Angela M. Christiano
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Angela M. Christianomedical Degrees
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Dermatology
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Angela M. Christianobiology Degrees
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Genetics
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Medical Biology
Angela M. Christiano's Degrees
- PhD Genetics and Development Columbia University
- Doctorate Medicine Columbia University
Why Is Angela M. Christiano Influential?
(Suggest an Edit or Addition)Angela M. Christiano's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Alopecia areata is driven by cytotoxic T lymphocytes and is reversed by JAK inhibition (2014) (636)
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity (2010) (631)
- Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa. (2000) (417)
- Alopecia universalis associated with a mutation in the human hairless gene. (1998) (413)
- Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia (1995) (394)
- Pseudoxanthoma elasticum: mutations in the MRP6 gene encoding a transmembrane ATP-binding cassette (ABC) transporter. (2000) (383)
- Mutations in the 180–kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa (1995) (360)
- Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion Evidence from Inherited Hypotrichosis and Acquired Pemphigus Vulgaris (2003) (337)
- Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ–5) (1994) (332)
- Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization. (1996) (315)
- Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study (2017) (302)
- Mutations in the γ2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa (1994) (302)
- The dermal-epidermal junction. (1997) (278)
- Generation of keratinocytes from normal and recessive dystrophic epidermolysis bullosa-induced pluripotent stem cells (2011) (264)
- Exposing the human nude phenotype (1999) (258)
- Microenvironmental reprogramming by three-dimensional culture enables dermal papilla cells to induce de novo human hair-follicle growth (2013) (251)
- Alopecia areata: Disease characteristics, clinical evaluation, and new perspectives on pathogenesis. (2017) (249)
- A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome (1996) (243)
- Safety and efficacy of the JAK inhibitor tofacitinib citrate in patients with alopecia areata. (2016) (240)
- Trans-gender induction of hair follicles (1999) (230)
- A homozygous nonsense mutation in the beta 3 chain gene of laminin 5 (LAMB3) in Herlitz junctional epidermolysis bullosa. (1994) (229)
- Hair follicle predetermination. (2001) (225)
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex (2010) (214)
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair (2008) (207)
- Oral ruxolitinib induces hair regrowth in patients with moderate-to-severe alopecia areata. (2016) (204)
- Hair follicle stem cells. (2003) (200)
- Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci (2015) (199)
- A missense mutation in type VII collagen in two affected siblings with recessive dystrophic epidermolysis bullosa (1993) (199)
- Cloning of human type VII collagen. Complete primary sequence of the alpha 1(VII) chain and identification of intragenic polymorphisms. (1994) (196)
- Reversal of Alopecia Areata Following Treatment With the JAK1/2 Inhibitor Baricitinib (2015) (193)
- Epitope mapping of type VII collagen. Identification of discrete peptide sequences recognized by sera from patients with acquired epidermolysis bullosa. (1993) (187)
- The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia (2006) (186)
- Structural organization of the human type VII collagen gene (COL7A1), composed of more exons than any previously characterized gene. (1994) (185)
- Generation of 3D Skin Equivalents Fully Reconstituted from Human Induced Pluripotent Stem Cells (iPSCs) (2013) (182)
- Alopecia areata (2017) (174)
- The role of the hairless (hr) gene in the regulation of hair follicle catagen transformation. (1999) (174)
- Classification of pseudoxanthoma elasticum: report of a consensus conference. (1994) (174)
- Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formation. (1997) (168)
- Amelioration of epidermolysis bullosa by transfer of wild-type bone marrow cells. (2009) (166)
- Pumpless microfluidic platform for drug testing on human skin equivalents. (2015) (164)
- The molecular pathology of progressive symmetric erythrokeratoderma: a frameshift mutation in the loricrin gene and perturbations in the cornified cell envelope. (1997) (157)
- Pharmacologic inhibition of JAK-STAT signaling promotes hair growth (2015) (153)
- Rapid skin repigmentation on oral ruxolitinib in a patient with coexistent vitiligo and alopecia areata (AA). (2016) (152)
- Molecular genetics of the cutaneous basement membrane zone. Perspectives on epidermolysis bullosa and other blistering skin diseases. (1992) (151)
- Human Skin Constructs with Spatially Controlled Vasculature Using Primary and iPSC‐Derived Endothelial Cells (2016) (151)
- The functions of laminins: lessons from in vivo studies. (1996) (148)
- Genomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areata. (2007) (145)
- Molecular basis of the dystrophic and junctional forms of epidermolysis bullosa: mutations in the type VII collagen and kalinin (laminin 5) genes. (1994) (143)
- Compound heterozygosity for non-sense and mis-sense mutations in desmoplakin underlies skin fragility/woolly hair syndrome. (2002) (140)
- Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene. (2001) (137)
- Dominant dystrophic epidermolysis bullosa: identification of a Gly-->Ser substitution in the triple-helical domain of type VII collagen. (1994) (136)
- The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases. (1997) (135)
- Altered laminin 5 expression due to mutations in the gene encoding the beta 3 chain (LAMB3) in generalized atrophic benign epidermolysis bullosa. (1995) (133)
- Tissue engineering of human hair follicles using a biomimetic developmental approach (2018) (133)
- Premature termination codons in the type VII collagen gene (COL7A1) underlie severe, mutilating recessive dystrophic epidermolysis bullosa. (1994) (129)
- Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16. (1996) (122)
- P-cadherin is a p63 target gene with a crucial role in the developing human limb bud and hair follicle (2008) (121)
- An Open-Label Pilot Study to Evaluate the Efficacy of Tofacitinib in Moderate to Severe Patch-Type Alopecia Areata, Totalis, and Universalis. (2018) (120)
- Elevated expression of type VII collagen in the skin of patients with systemic sclerosis. Regulation by transforming growth factor-beta. (1994) (116)
- FGF5 is a crucial regulator of hair length in humans (2014) (116)
- Glycine substitutions in the triple-helical region of type VII collagen result in a spectrum of dystrophic epidermolysis bullosa phenotypes and patterns of inheritance. (1996) (115)
- A homozygous insertion–deletion in the type VII collagen gene (COL7A1) in Hallopeau–Siemens dystrophic epidermolysis bullosa (1993) (115)
- Strategy for identification of sequence variants in COL7A1 and a novel 2‐bp deletion mutation in recessive dystrophic epidermolysis bullosa (1997) (111)
- Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition. (1996) (111)
- Induced pluripotent stem cells from human revertant keratinocytes for the treatment of epidermolysis bullosa (2014) (110)
- Cloning of the laminin alpha 3 chain gene (LAMA3) and identification of a homozygous deletion in a patient with Herlitz junctional epidermolysis bullosa. (1995) (107)
- A 30 kb deletion within the elastin gene results in familial supravalvular aortic stenosis. (1995) (103)
- Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis. (2009) (102)
- Mutational hotspots in the LAMB3 gene in the lethal (Herlitz) type of junctional epidermolysis bullosa. (1996) (102)
- Melanin Transfer in Human 3D Skin Equivalents Generated Exclusively from Induced Pluripotent Stem Cells (2015) (94)
- Site-specific genome editing for correction of induced pluripotent stem cells derived from dominant dystrophic epidermolysis bullosa (2016) (93)
- Desmoglein 4 is expressed in highly differentiated keratinocytes and trichocytes in human epidermis and hair follicle. (2006) (91)
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis. (2007) (90)
- Mechanisms and Disease Associations of Haplotype-Dependent Allele-Specific DNA Methylation. (2016) (89)
- Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions. (2001) (89)
- Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family. (1999) (88)
- A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1. (1998) (87)
- Biology and genetics of hair. (2010) (87)
- Type VII collagen gene expression by cultured human cells and in fetal skin. Abundant mRNA and protein levels in epidermal keratinocytes. (1992) (84)
- A Subset of TREM2+ Dermal Macrophages Secretes Oncostatin M to Maintain Hair Follicle Stem Cell Quiescence and Inhibit Hair Growth. (2019) (83)
- Molecular basis of recessive dystrophic epidermolysis bullosa: genotype/phenotype correlation in a case of moderate clinical severity. (1996) (81)
- Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture. (2010) (81)
- A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers. (1998) (80)
- KGF and EGF signalling block hair follicle induction and promote interfollicular epidermal fate in developing mouse skin (2009) (80)
- Structural and functional consequences of loricrin mutations in human loricrin keratoderma (Vohwinkel syndrome with ichthyosis). (2004) (79)
- Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions. (2006) (79)
- Identification of Two Novel Human Acyl-CoA Wax Alcohol Acyltransferases (2005) (77)
- Patterns of hairless (hr) gene expression in mouse hair follicle morphogenesis and cycling. (2000) (75)
- Recurrent nonsense mutations within the type VII collagen gene in patients with severe recessive dystrophic epidermolysis bullosa. (1994) (73)
- Treatment of an alopecia areata patient with tofacitinib results in regrowth of hair and changes in serum and skin biomarkers (2016) (73)
- CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells (2019) (72)
- Mutations in the non-helical linker segment L1-2 of keratin 5 in patients with Weber-Cockayne epidermolysis bullosa simplex. (1994) (72)
- Novel molecular therapies for heritable skin disorders. (2012) (70)
- Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa. (1997) (70)
- Molecular signatures define alopecia areata subtypes and transcriptional biomarkers (2016) (70)
- Congenital atrichia in five Arab Palestinian families resulting from a deletion mutation in the human hairless gene (1998) (70)
- Next generation human skin constructs as advanced tools for drug development (2017) (69)
- Identification of C7orf11 (TTDN1) gene mutations and genetic heterogeneity in nonphotosensitive trichothiodystrophy. (2005) (67)
- The large non-collagenous domain (NC-1) of type VII collagen is amino-terminal and chimeric. Homology to cartilage matrix protein, the type III domains of fibronectin and the A domains of von Willebrand factor. (1992) (66)
- Germline fumarate hydratase mutations in families with multiple cutaneous and uterine leiomyomata. (2003) (66)
- Genetic basis of dominantly inherited transient bullous dermolysis of the newborn: a splice site mutation in the type VII collagen gene. (1997) (65)
- Pretibial epidermolysis bullosa: genetic linkage to COL7A1 and identification of a glycine-to-cysteine substitution in the triple-helical domain of type VII collagen. (1995) (65)
- FUN-LDA: A LATENT DIRICHLET ALLOCATION MODEL FOR PREDICTING TISSUE-SPECIFIC FUNCTIONAL EFFECTS OF NONCODING VARIATION (2017) (65)
- Human equivalent of the mouse Nude/SCID phenotype: long-term evaluation of immunologic reconstitution after bone marrow transplantation. (2001) (65)
- Molecular basis for the dystrophic forms of epidermolysis bullosa: mutations in the type VII collagen gene (2004) (64)
- Genetic basis of Bart's syndrome: a glycine substitution mutation in type VII collagen gene. (1996) (64)
- Sequential Loss of Two Neighboring Exons of the Tropoelastin Gene During Primate Evolution (1999) (63)
- A homozygous deletion mutation in the gene encoding the 180-kDa bullous pemphigoid antigen (BPAG2) in a family with generalized atrophic benign epidermolysis bullosa. (1996) (63)
- Molecular diagnosis of inherited skin diseases: the paradigm of dystrophic epidermolysis bullosa. (1996) (63)
- Premature termination codon mutations in the type VII collagen gene in recessive dystrophic epidermolysis bullosa result in nonsense-mediated mRNA decay and absence of functional protein. (1997) (62)
- Production-scale fibronectin nanofibers promote wound closure and tissue repair in a dermal mouse model. (2018) (62)
- Workshop on pseudoxanthoma elasticum: molecular biology and pathology of the elastic fibers. Jefferson Medical College, Philadelphia, Pennsylvania, June 10, 1992. (1992) (62)
- Tofacitinib for the treatment of lichen planopilaris: A case series (2018) (62)
- Molecular pathology of the elastic fibers. (1994) (62)
- Progress Towards Treatment and Cure of Epidermolysis Bullosa: Summary of the DEBRA International Research Symposium EB2015 (2015) (61)
- Epithelial Stem Cells Stepping out of Their Niche (2004) (61)
- Activation of Notch1 in the hair follicle leads to cell-fate switch and Mohawk alopecia. (2004) (59)
- A multi-organ chip with matured tissue niches linked by vascular flow (2022) (59)
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice. (2008) (58)
- Recurrent mutations in the type VII collagen gene (COL7A1) in patients with recessive dystrophic epidermolysis bullosa. (1997) (58)
- Cloning of the β3 chain gene (LAMB3) of human laminin 5, a candidate gene in junctional epidermolysis bullosa (1995) (57)
- Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata. (2005) (57)
- CXCR3 Blockade Inhibits T Cell Migration into the Skin and Prevents Development of Alopecia Areata (2016) (56)
- Multiple familial cutaneous glomangioma: a pedigree of 4 generations and critical analysis of histologic and genetic differences of glomus tumors. (2000) (55)
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene. (2004) (54)
- Differential cytokine modulation of the genes LAMA3, LAMB3, and LAMC2, encoding the constitutive polypeptides, α3, β3, and γ2, of human laminin 5 in epidermal keratinocytes (1995) (54)
- MUTATION‐BASED PRENATAL DIAGNOSIS OF HERLITZ JUNCTIONAL EPIDERMOLYSIS BULLOSA (1997) (53)
- Mammalian tropoelastin: multiple domains of the protein define an evolutionarily divergent amino acid sequence. (1991) (53)
- A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk. (1995) (53)
- Clinicopathological correlations of compound heterozygous COL7A1 mutations in recessive dystrophic epidermolysis bullosa. (1996) (52)
- Mutations in R-spondin 4 (RSPO4) underlie inherited anonychia. (2008) (52)
- A glycine-to-arginine substitution in the triple-helical domain of type VII collagen in a family with dominant dystrophic epidermolysis bullosa. (1997) (51)
- Influence of the second COL7A1 mutation in determining the phenotypic severity of recessive dystrophic epidermolysis bullosa. (1996) (50)
- Niche Crosstalk: Intercellular Signals at the Hair Follicle (2011) (50)
- Trps1 and Its Target Gene Sox9 Regulate Epithelial Proliferation in the Developing Hair Follicle and Are Associated with Hypertrichosis (2012) (50)
- Molecular basis for the rhino (hrrh-8J) phenotype: a nonsense mutation in the mouse hairless gene. (1998) (49)
- Premature termination codons are present on both alleles of the bullous pemphigoid antigen 2/type XVII collagen gene in five Austrian families with generalized atrophic benign epidermolysis bullosa. (1997) (49)
- Whole-exome sequencing in a single proband reveals a mutation in the CHST8 gene in autosomal recessive peeling skin syndrome. (2012) (48)
- JAK Inhibitors for Treatment of Alopecia Areata. (2018) (48)
- Broken hearts, woolly hair, and tattered skin: when desmosomal adhesion goes awry. (2007) (48)
- DNA-based prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa in six pregnancies at risk for recurrence. (1995) (47)
- Glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: implications for genetic counseling. (1997) (47)
- Characterization of Desmoglein Expression in the Normal Prostatic Gland. Desmoglein 2 Is an Independent Prognostic Factor for Aggressive Prostate Cancer (2014) (47)
- Compound heterozygosity for COL7A1 mutations in twins with dystrophic epidermolysis bullosa: a recessive paternal deletion/insertion mutation and a dominant negative maternal glycine substitution result in a severe phenotype. (1996) (47)
- Molecular biology and pathology of human elastin. (1991) (46)
- Human Cord Blood-Derived Unrestricted Somatic Stem Cells Promote Wound Healing and have Therapeutic Potential for Patients with Recessive Dystrophic Epidermolysis Bullosa (2014) (45)
- Premature termination codons on both alleles of the type VII collagen gene (COL7A1) in three brothers with recessive dystrophic epidermolysis bullosa. (1995) (45)
- The genetics of alopecia areata: What's new and how will it help our patients? (2011) (44)
- Genetic basis of alopecia areata: a roadmap for translational research. (2013) (44)
- Homozygous variegate porphyria: identification of mutations on both alleles of the protoporphyrinogen oxidase gene in a severely affected proband. (1998) (44)
- Health-Related Quality of Life (HRQoL) in alopecia areata patients-a secondary analysis of the National Alopecia Areata Registry Data. (2013) (44)
- Mutations in the keratin 85 (KRT85/hHb5) gene underlie pure hair and nail ectodermal dysplasia. (2010) (43)
- The molecular basis of congenital atrichia in humans and mice: mutations in the hairless gene. (1999) (43)
- Restoration of open reading frame resulting from skipping of an exon with an internal deletion in the COL7A1 gene. (1998) (43)
- Hairless is translocated to the nucleus via a novel bipartite nuclear localization signal and is associated with the nuclear matrix. (2001) (42)
- Clinical and pathologic correlations in genetically distinct forms of atrichia. (2003) (42)
- Trps1 activates a network of secreted Wnt inhibitors and transcription factors crucial to vibrissa follicle morphogenesis (2012) (42)
- Hereditary leukonychia, or porcelain nails, resulting from mutations in PLCD1. (2011) (42)
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome. (2011) (41)
- A recurrent intragenic deletion in the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis. (2004) (40)
- Pathomechanisms of immune-mediated alopecia. (2019) (40)
- Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis (2013) (40)
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation. (2009) (40)
- Bullous pemphigoid antigen: cDNA cloning, cellular expression, and evidence for polymorphism of the human gene. (1990) (39)
- Mutations in the Cholesterol Transporter Gene ABCA5 Are Associated with Excessive Hair Overgrowth (2014) (39)
- Cloning of the Gene for Human Pemphigus Vulgaris Antigen (Desmoglein 3), a Desmosomal Cadherin (1996) (39)
- Compound heterozygosity for nonsense ans missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosa. (1996) (39)
- The WNT signalling modulator, Wise, is expressed in an interaction-dependent manner during hair-follicle cycling. (2004) (39)
- Nothing but skin and bone. (2006) (39)
- Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22–q24 (2003) (39)
- Bone marrow stem cell therapy for recessive dystrophic epidermolysis bullosa. (2010) (38)
- Novel and de novo glycine substitution mutations in the type VII collagen gene (COL7A1) in dystrophic epidermolysis bullosa: implications for genetic counseling. (1998) (38)
- Predominance of the recurrent mutation R635X in the LAMB3 gene in European patients with Herlitz junctional epidermolysis bullosa has implications for mutation detection strategy. (1997) (38)
- A to G polymorphism in ELN gene. (1991) (37)
- A homozygous nonsense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia. (1999) (37)
- Morphological approach to hair disorders. (2003) (37)
- Evidence for extensive locus heterogeneity in Naxos disease. (2002) (36)
- PI3K/AKT pathway regulates E-cadherin and Desmoglein 2 in aggressive prostate cancer (2015) (36)
- Castration-mediated IL-8 promotes myeloid infiltration and prostate cancer progression (2019) (36)
- Human leukocyte antigen class II alleles are associated with risk of alopecia areata. (2008) (36)
- Alopecia areata is a medical disease. (2018) (35)
- Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis. (2009) (35)
- Hairless is a histone H3K9 demethylase (2014) (35)
- Building a microphysiological skin model from induced pluripotent stem cells (2013) (34)
- Dynamic expression of the zinc-finger transcription factor Trps1 during hair follicle morphogenesis and cycling. (2008) (34)
- Functional interpretation of genome-wide association study evidence in alopecia areata (2015) (34)
- The bulge is the source of cellular renewal in the sebaceous gland of mouse skin (2000) (34)
- Compound heterozygosity for nonsense and missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosa. (1996) (34)
- Premature termination codon mutations in the type VII collagen gene (COL7A1) underlie severe recessive dystrophic epidermolysis bullosa. (1995) (33)
- Multifaceted role of hair follicle dermal cells in bioengineered skins (2017) (33)
- DNA-based prenatal diagnosis of heritable skin diseases. (1993) (33)
- The Effect of Inbreeding on the Distribution of Compound Heterozygotes: A Lesson from Lipase H Mutations in Autosomal Recessive Woolly Hair/Hypotrichosis (2009) (33)
- NIPAL4/Ichthyin Is Expressed in the Granular Layer of Human Epidermis and Mutated in Two Pakistani Families with Autosomal Recessive Ichthyosis (2009) (32)
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity. (2008) (32)
- Nail dystrophy associated with a heterozygous mutation of the nude/SCID human FOXN1 (WHN) gene. (2005) (32)
- A novel homozygous nonsense mutation in the LAMC2 gene in patients with the Herlitz junctional epidermolysis bullosa. (1994) (32)
- High-throughput T cell receptor sequencing identifies clonally expanded CD8+ T cell populations in alopecia areata. (2018) (31)
- Differential structural properties and expression patterns suggest functional significance for multiple mouse desmoglein 1 isoforms. (2004) (31)
- Frontiers in keratodermas: pushing the envelope. (1997) (31)
- Evidence for pseudodominant inheritance of atrichia with papular lesions. (2002) (30)
- A recurrent homozygous nonsense mutation within the LAMA3 gene as a cause of Herlitz junctional epidermolysis bullosa in patients of Pakistani ancestry: evidence for a founder effect. (1996) (30)
- A missense mutation in the cadherin interaction site of the desmoglein 4 gene underlies localized autosomal recessive hypotrichosis. (2005) (30)
- Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation. (2008) (30)
- A spontaneous mutation in the desmoglein 4 gene underlies hypotrichosis in a new lanceolate hair rat model. (2004) (29)
- Multiple cutaneous and uterine leiomyomas: refinement of the genetic locus for multiple cutaneous and uterine leiomyomas on chromosome 1q42.3-43. (2002) (29)
- A Nonsense Mutation in the SCN9A Gene in Congenital Insensitivity to Pain (2010) (29)
- Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase gene (1996) (29)
- Variegate Porphyria: Past, Present and Future (1998) (28)
- Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene cluster. (1993) (28)
- First trimester DNA‐based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus sampling (1996) (27)
- Reduced Toxicity Conditioning and Allogeneic Hematopoietic Progenitor Cell Transplantation for Recessive Dystrophic Epidermolysis Bullosa. (2015) (27)
- A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance (2011) (27)
- Localized autosomal recessive hypotrichosis due to a frameshift mutation in the desmoglein 4 gene exhibits extensive phenotypic variability within a Pakistani family. (2007) (27)
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo "hairless" rat. (2004) (27)
- Identification of a Founder Mutation in the Protoporphyrinogen Oxidase Gene in Variegate Porphyria Patients from Chile (2001) (26)
- Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome (2004) (26)
- Detection of Novel LAMC2 Mutations in Herlitz Junctional Epidermolysis Bullosa (1997) (26)
- Complex cytogenetic rearrangement of chromosome 8q in a case of Ambras syndrome. (2001) (26)
- STXBP4 regulates APC/C-mediated p63 turnover and drives squamous cell carcinogenesis (2018) (25)
- Recapitulating T cell infiltration in 3D psoriatic skin models for patient-specific drug testing (2020) (25)
- Inherited disorders of the skin in human and mouse: from development to differentiation. (2004) (25)
- Cloning of mouse type VII collagen reveals evolutionary conservation of functional protein domains and genomic organization. (1996) (25)
- A common insertion mutation in COL7A1 in two Italian families with recessive dystrophic epidermolysis bullosa. (1996) (25)
- Loss of Hairless Confers Susceptibility to UVB-Induced Tumorigenesis via Disruption of NF-kappaB Signaling (2012) (24)
- Mutations in the desmoglein 1 gene in five Pakistani families with striate palmoplantar keratoderma. (2009) (23)
- Compound heterozygosity for a nonsense mutation and a splice site mutation in the type VII collagen gene (COL7A1) in recessive dystrophic epidermolysis bullosa. (1997) (23)
- Alopecia areata registry: an overview. (2003) (23)
- Compound heterozygous mutations in the hairless gene in atrichia with papular lesions. (2003) (23)
- Genetic linkage studies in alopecia areata. (2003) (23)
- The Genetic Bases of the Porphyrias (1998) (23)
- Maternal germline mosaicism in dominant dystrophic epidermolysis bullosa. (2001) (23)
- Master regulators of infiltrate recruitment in autoimmune disease identified through network-based molecular deconvolution. (2015) (23)
- cDNA cloning and chromosomal mapping of the mouse type VII collagen gene (Col7a1): evidence for rapid evolutionary divergence of the gene. (1993) (23)
- Dystrophic forms of epidermolysis bullosa. (1993) (23)
- Regenerative medicine and hair loss: how hair follicle culture has advanced our understanding of treatment options for androgenetic alopecia. (2014) (23)
- The genetics of human skin disease. (2014) (22)
- Striate palmoplantar keratoderma resulting from a frameshift mutation in the desmoglein 1 gene. (2007) (22)
- Molecular analysis of the human laminin alpha3a chain gene (LAMA3a): a strategy for mutation identification and DNA-based prenatal diagnosis in Herlitz junctional epidermolysis bullosa. (1998) (22)
- Reprogramming of human hair follicle dermal papilla cells into induced pluripotent stem cells. (2012) (22)
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene (2002) (22)
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2 (2017) (21)
- Hairless contains a novel nuclear matrix targeting signal and associates with histone deacetylase 3 in nuclear speckles. (2004) (21)
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- Complete coding sequence, intron/exon organization, and chromosomal location of the gene for the core I protein of human ubiquinol-cytochrome c reductase. (1993) (20)
- The genetic architecture of alopecia areata. (2013) (20)
- The molecular genetics of dystrophic epidermolysis bullosa. (1993) (20)
- Identification of mutations in the transgluataminase 1 gene in lamellar ichthyosis (1999) (19)
- Mutations in the SLURP-1 gene underlie Mal de Meleda in three Pakistani families. (2009) (19)
- Mutations in the LIPH gene in three Japanese families with autosomal recessive woolly hair/hypotrichosis. (2009) (19)
- Variegate porphyria: identification of a nonsense mutation in the protoporphyrinogen oxidase gene. (1998) (19)
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias (2018) (19)
- Cord Blood‐Derived Stem Cells Suppress Fibrosis and May Prevent Malignant Progression in Recessive Dystrophic Epidermolysis Bullosa (2018) (18)
- PCR-based detection of two exonic polymorphisms in the human type VII collagen gene (COL7A1) at 3p21.1. (1992) (18)
- Recurrent missense mutation in the protoporphyrinogen oxidase gene underlies variegate porphyria. (1998) (18)
- The Changing Landscape of Alopecia Areata: The Translational Landscape (2017) (18)
- Atrichia with papular lesions resulting from compound heterozygous mutations in the hairless gene: A lesson for differential diagnosis of alopecia universalis. (2002) (18)
- Identification of the glycine‐to‐arginine substitution G2043R in type VII collagen in a family with dominant dystrophic epidermolysis bullosa from Hungary (1997) (18)
- EB simplex superficialis resulting from a mutation in the type VII collagen gene. (2002) (17)
- Cloning of the beta 3 chain gene (LAMB3) of human laminin 5, a candidate gene in junctional epidermolysis bullosa. (1995) (17)
- Absence of R42X and R635X mutations in the LAMB3 gene in 12 Japanese patients with junctional epidermolysis bullosa (1997) (17)
- Nonsense mutations in the hairless gene underlie APL in five families of Pakistani origin. (2007) (17)
- Hoxa4 expression in developing mouse hair follicles and skin (2000) (16)
- Erythropoietic protoporphyria: identification of novel mutations in the ferrochelatase gene and comparison of biochemical markers versus molecular analysis as diagnostic strategies. (1999) (16)
- Early‐Onset Heart Failure, Alopecia, and Cutaneous Abnormalities Associated with a Novel Compound Heterozygous Mutation in Desmoplakin (2015) (16)
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy (2020) (16)
- Childhood alopecia areata—Data from the National Alopecia Areata Registry (2018) (16)
- The genetic basis of “Scarsdale Gourmet Diet” variegate porphyria: a missense mutation in the protoporphyrinogen oxidase gene (1998) (15)
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- Molecular basis of congenital atrichia in humans and mice. (1999) (15)
- Identification of a glycine substitution and a splice site mutation in the type VII collagen gene in a proband with mitis recessive dystrophic epidermolysis bullosa (1997) (15)
- Molecular basis of variegate porphyria: a missense mutation in the protoporphyrinogen oxidase gene. (1998) (15)
- A spectrum of novel mutations in the protoporphyrinogen oxidase gene in 13 families with variegate porphyria. (2001) (15)
- Interaction of hairless and thyroid hormone receptor is not involved in the pathogenesis of atrichia with papular lesions (2004) (15)
- Expression patterns of the transcription factor AP-2alpha during hair follicle morphogenesis and cycling. (2003) (14)
- Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats. (2005) (14)
- Stem Cells in the Epidermis (2001) (14)
- Novel compound heterozygous nonsense mutations in the hairless gene causing atrichia with papular lesions. (2005) (14)
- Abnormal cornified cell envelope formation in mutilating palmoplantar keratoderma unrelated to epidermal differentiation complex. (1998) (14)
- Allele-specific DNA methylation is increased in cancers and its dense mapping in normal plus neoplastic cells increases the yield of disease-associated regulatory SNPs (2019) (14)
- Evidence for a Founder Mutation in the Cathepsin C Gene in Three Families with Papillon-Lefèvre Syndrome (2009) (14)
- Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata. (2017) (13)
- Novel therapies for alopecia areata: The era of rational drug development (2017) (13)
- Identification of differentially expressed miRNAs in alopecia areata that target immune-regulatory pathways (2017) (13)
- Challenges and promises in modeling dermatologic disorders with bioengineered skin (2014) (13)
- Erythropoietic protoporphyria: four novel frameshift mutations in the ferrochelatase gene. (1997) (13)
- Pathobiology of the hairless phenotype: Dysregulation of hair follicle apoptosis and topobiology during the initiation of follicle cycling (1998) (13)
- Identification of Distinct Mutations in AAGAB in Families with Type 1 Punctate Palmoplantar Keratoderma (2014) (12)
- Shedding Light on Alopecia Areata in Pediatrics: A Retrospective Analysis of Comorbidities in Children in the National Alopecia Areata Registry (2017) (12)
- Rapid prenatal diagnosis of sickle cell diseases using oligonucleotide ligation assay coupled with laser‐induced capillary fluorescence detection (2002) (12)
- Identification of a novel splice site mutation in the human hairless gene underlying atrichia with papular lesions. (2005) (12)
- The single copy gene coding for human α1 (IV) procollagen is located at the terminal end of the long arm of chromosome 13 (1986) (12)
- Epidermolytic palmoplantar keratoderma in a Hispanic kindred resulting from a mutation in the keratin 9 gene (2000) (11)
- Genetics of Structural Hair Disorders. (2012) (11)
- Copy Number Variations on Chromosome 4q26–27 Are Associated with Cantu Syndrome (2012) (11)
- JAK-STAT Signaling Jump Starts the Hair Cycle. (2016) (11)
- Efficacy of Human Placental‐Derived Stem Cells in Collagen VII Knockout (Recessive Dystrophic Epidermolysis Bullosa) Animal Model (2018) (10)
- Polymorphism of the human genome: markers for genetic linkage analyses in heritable diseases of the skin. (1992) (10)
- In vivo enhanced expression of patched dampens the sonic hedgehog pathway. (2002) (10)
- Bumps and pumps, SERCA 1999 (1999) (10)
- A Common Founder Mutation in the EDA-A1 Gene in X-Linked Hypodontia (2010) (9)
- Genetic basis of Bart's syndrome: a glycine substitution mutation in the type VII collagen gene. (1996) (9)
- Keratin 71 mutations: from water dogs to woolly hair. (2012) (9)
- Extensive alternate exon usage at the 5' end of the sheep tropoelastin gene. (1995) (9)
- Mutations in the hairless gene underlie APL in three families of Pakistani origin. (2008) (9)
- An open-label study evaluating the efficacy of abatacept in alopecia areata. (2020) (8)
- Hair follicle disruption facilitates pathogenesis to UVB-induced cutaneous inflammation and basal cell carcinoma development in Ptch(+/-) mice. (2014) (8)
- Genomic Organization of Mouse Desmocollin Genes Reveals Evolutionary Conservation (2004) (8)
- Medical Comorbidities and Gender Distribution Among Patients with Lichen Planopilaris and Frontal Fibrosing Alopecia: A Retrospective Cohort Study. (2020) (8)
- Validation of Case Identification for Alopecia Areata Using International Classification of Diseases Coding (2020) (8)
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis (2013) (8)
- Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A gene (2013) (8)
- Blockade of IL-7 signaling suppresses inflammatory responses and reverses alopecia areata in C3H/HeJ mice (2021) (8)
- The Charles River "hairless" rat mutation is distinct from the hairless mouse alleles. (2001) (8)
- Alopecia areata. (1977) (7)
- Genomic organization and analysis of the hairless gene in four hypotrichotic rat strains (2004) (7)
- Restoration of open reading frame due to skipping of an exon with an internal deletion in the COL7A1 gene (1998) (7)
- Hair follicle epithelial stem cells get their sox on. (2008) (7)
- Recapitulation of the hairless mouse phenotype using catalytic oligonucleotides: implications for permanent hair removal (2004) (7)
- 649 Gut microbiota plays a role in the development of alopecia areata (2017) (7)
- The pro alpha 1 (IV) collagen gene is linked to the D13S3 locus at the distal end of human chromosome 13q. (1987) (6)
- Tissue-specific functional effect prediction of genetic variation and applications to complex trait genetics (2016) (6)
- Acne chlorina and acne vulgaris – casual likeness or causal homology? (2000) (6)
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82 (2022) (5)
- Genome-wide linkage analysis of an autosomal recessive hypotrichosis identi fi es a novel P 2 RY 5 mutation (2008) (5)
- Fibrillin immunofluorescence in pseudoxanthoma elasticum. (1995) (5)
- Collagen VII in severe recessive dystrophic epidermolysis bullosa: expression of mRNA but lack of intact protein product in skin and cutaneous cells in vitro. (1994) (5)
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- Apcdd1 is a dual BMP/Wnt inhibitor in the developing nervous system and skin (2019) (5)
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- Mutations in the Laminin 5 LAMB3 Gene in Generalized Atrophic Benign Epidermolysis Bullosa (1995) (5)
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- There and back again: hair follicle stem cell dynamics. (2011) (4)
- Demystification of Chester porphyria: a nonsense mutation in the Porphobilinogen Deaminase gene. (2006) (3)
- Preimplantation genetic diagnosis in a family at risk for recurrence of Herlitz junctional epidermolysis bullosa (1998) (3)
- PCR-based detection of intragenic RFLPs in the human type VII collagen gene: Applications to prenatal diagnosis of dystrophic epidermolysis bullosa (1993) (3)
- Molecular characterization of Blau syndrome: Genetic linkage to chromosome 16 (1994) (3)
- A glycine substitution in the COL7A1 gene causes mild RDEB in a Pakistani family. (2006) (3)
- Genetics of structural hair disorders. (2012) (3)
- A semi-supervised model to predict regulatory effects of genetic variants at single nucleotide resolution using massively parallel reporter assays. (2021) (3)
- Hair Follicle Dermal Cells Support Expansion of Murine and Human Embryonic and Induced Pluripotent Stem Cells and Promote Haematopoiesis in Mouse Cultures (2018) (3)
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- Improved therapeutic efficacy of unmodified anti-tumor antibodies by immune checkpoint blockade and kinase targeted therapy in mouse models of melanoma (2021) (2)
- Mutations in the laminin 5 genes (LAMB3 and LAMC2) in patients with the junctional forms of epidermolysis bullosa (JEB) (1994) (2)
- Inherited Disorders of the Hair (2013) (2)
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- Search for susceptibility genes in alopecia areata. (2005) (2)
- Heterogeneity of mutations in the type VII collagen gene (COL7A1) in different forms of dystrophic epidermolysis bullosa (1994) (2)
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- Junctional Forms of Epidermolysis Bullosa (1998) (2)
- Settling the score on hairless. (2000) (2)
- Impaired autophagy promotes hair loss in the C3H/HeJ mouse model of alopecia areata (2022) (2)
- The Role of MMAC 1 Mutations in Early-Onset Breast Cancer : Causative in Association with Cowden Syndrome and Excluded in BRCA 1-Negative Cases (2006) (2)
- 691 Topical curcumin promotes induction of the murine hair cycle (2016) (2)
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- 085 Autoantigen screening in C3H/HeJ mouse model of alopecia areata revealed high antigenicity of melanocyte-associated antigen epitopes (2019) (1)
- Correction of the Skin Defect in Murine Recessive Dystrophic Epidermolysis Bullosa by Bone Marrow Derived SLAM Family Receptor Enriched Cells. (2007) (1)
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- 320 An open label clinical trial of Abatacept (CTLA4-Ig) for alopecia areata (2017) (1)
- Generation of induced pluripotent stem cells from revertant mosaic keratinocytes: A novel strategy for natural gene therapy for epidermolysis bullosa (2013) (1)
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- Characterization of mutations in the type VII collagen gene in patients with the dystrophic forms of epidermolysis bullosa (1993) (1)
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3 (2014) (1)
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- Detection of Novel LAMC 2 Mutations in Herlitz Junctional Epidermolysis Bullosa (2007) (1)
- 190 Biallelic correction of recessive dystrophic epidermolysis bullosa mutations in iPSCs using CRISPR/Cas9- based genome editing (2017) (1)
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- Termination Codons on Both Alleles of the Type VIl Collagen Gene ( COL 7 A 1 ) in Three Brothers with Recessive Dystrophic Epidermolysis Bullosa (2013) (1)
- 455 Molecular correlation with clinical outcomes in an open label clinical trial of oral tofacitinib in patients with alopecia areata (2018) (1)
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- A recurrent premature termination codon mutation (498insA) in the type VII collagen gene (COL7A1) in two unrelated families with recessive dystrophic epidermolysis bullosa (RDEB) in Italy (1994) (0)
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- 475 Targeting the JAK/STAT3 pathway with ruxolitinib for RDEB-cSCC therapy (2019) (0)
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- Epidermal Health and Disease Desmosomes : Regulators of Cellular Signaling and Adhesion in Subject Collection The Skin and Its Diseases Immunology and Skin in Health and Disease (2014) (0)
- 054 Regulatory natural killer cells are protective in alopecia areata (2017) (0)
- 798 Biallelic COL7A1 editing in iPSCs via CRISPR/Cas9 for recessive dystrophic epidermolysis bullosa mutations (2018) (0)
- Medical Comorbidities and Gender Distribution Among Patients with Lichen Planopilaris and Frontal Fibrosing Alopecia: A Retrospective Cohort Study- Supplementary Methods (2020) (0)
- 099 Identification of T cell receptor chains responsible for alopecia areata pathogenesis via bulk and single cell TCR sequencing (2018) (0)
- 399 Expression quantitative trait loci (eQTL) mapping in a multicenter cross-sectional study of Alopecia Areata (2016) (0)
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- 397 Predictive modeling of drug response and mechanism of action in alopecia areata clinical trials (2017) (0)
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- 073 Identification of alopecia areata autoantigens in C3H/HeJ mice using whole-skin homogenates (2018) (0)
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- 413 One-step iPSC-reprogramming and genome-editing on primary fibroblasts using CRISPR/Cas9 ribonuleoprotein approach for recessive dystrophic epidermolysis bullosa (2019) (0)
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- 706 Predictive modeling of patient response to JAK/STAT inhibitors and dynamic patient-matching (2019) (0)
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- Transplantation of hair follicle dermal cells as a therapeutic approach for recessive dystrophic epidermolysis bullosa (2013) (0)
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- 1039 Novel mouse model of recessive dystrophic epidermolysis bullosa-squamous cell carcinoma (2019) (0)
- 052 Identification of pathogenic T cell subsets in human alopecia areata (2017) (0)
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- 441 Targeting glycolysis metabolism prevents the onset of alopecia areata in C3H/HeJ mice (2019) (0)
- Promotion of Wound Healing by Cord Blood Derived Unrestricted Somatic Stem Cells (USSCs) in a Murine Wound Healing Model and Analysis on Their Bio-Distribution by In Vivo Bioluminescent Imaging (BLI) (2013) (0)
- 908 Keratinocytes and fibroblasts facilitate maturation of sensory neurons differentiated from human induced pluripotent stem cells (2017) (0)
- 1210 Enhancing the therapeutic efficacy of immune checkpoint inhibition and targeted therapy using anti-tumor antibodies in mouse melanoma (2018) (0)
- 746 Differentiation of sensory neurons from human induced pluripotent stem cells (2016) (0)
- 1123. Adenovirus-Mediated Expression of Sonic Hedgehog Increases the Number of CD34+ Cells in the Epidermal Stem Cell Niche in Hair Follicles (2005) (0)
- 301 Whole exome sequencing in AA patients identifies a hotspot mutation in the type II hair keratin gene, KRT82 (2020) (0)
- 470 The gut microbiome is required for the development of alopecia areata (2016) (0)
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- Abstract 1510: Androgen regulated IL-8 expression in prostate cancer: Insights into tumor cell mediated immunosuppression (2019) (0)
- Special issue on epidermal and hair follicle differentiation, part 2 (2004) (0)
- Abnormal cornified cell envelope formation in mutilating palmoplantar keratoderma unrelated to epidermal differentiation complex (1998) (0)
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- Human Umbilical Cord Blood (HUCB) Derived Stem Cells Enhances Wound Healing (2012) (0)
- Genetic Hair and Nail Defects (2006) (0)
- 438 Pharmacological inhibition of leptin delays anagen in the murine hair cycle (2019) (0)
- 028 Large-scale screening for T cell epitopes in human alopecia areata (2017) (0)
- 863 Central centrifugal cicatricial alopecia gene expression analysis revealed cholesterol, fatty acid, and mast cell pathways (2019) (0)
- Sa1344 Celiac Disease-Associated Antibodies in the Phenotypic Spectrum of Alopecia Areata (2012) (0)
- 101 Alopecia areata is reversed by IL-7Rα blockade via upregulation of the PD-1 signaling pathway and T cell exhaustion (2018) (0)
- Analysing the mechanisms of follicle dermal cell aggregation and induction: a cell and molecular study (2005) (0)
- Studies uncover new approaches to combat hair loss in men and women (2020) (0)
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- Department of Clinical Chemistry University of Helsinki MOLECULAR GENETICS OF AUTOSOMAL RECESSIVE CONGENITAL ICHTHYOSIS (2000) (0)
- 216 Master regulators of immune infiltrate recruitment improve efficacy of immune checkpoint inhibitor therapy in melanomas (2018) (0)
- Complete characterization of the human type VII collagen gene (1993) (0)
- Human Umbilical Cord Blood (HUCB) Derived Pluripotent Stem Cells Enhances Wound Healing (2011) (0)
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- 519 The role of the leaky gut in the development of alopecia areata (2019) (0)
- Mutations in the LAMB3 gene in the generalized atrophic benign form of junctional epidermolysis bullosa (1994) (0)
- 462 Clinical improvement in primary cicatricial alopecias following mast cell stabilizer treatment (2021) (0)
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- 307 Computer-assisted epitope prediction revealed potential autoantigens associated with human alopecia areata (2018) (0)
- 07-P006 A new in situ study of the cellular and molecular basis of adipogenesis using developing mouse skin (2009) (0)
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- 780 Rare genetic mutations contribute to alopecia areata etiology and provide rationale for sequencing patient genomes (2018) (0)
- 198 The JAK1/2 inhibitor ruxolitinib induces cell cycle arrest and apoptosis through inhibiting STAT3 phosphorylation in squamous cell carcinoma (2018) (0)
- Variegate porphyria: Identification of 10 novel mutations in the protoporphyrinogen oxidase gene (1998) (0)
- 924 Efficient genome editing using CRISPR/Cas9 ribonucleoprotein approach in iPS cells for recessive dystrophic epidermolysis bullosa (2019) (0)
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- Collagen Gene Expression by Cultured Human Cells and in Fetal Skin Abundant mRNAand Protein Levels in Epidermal Keratinocytes (2013) (0)
- Subject Index Vol. 11, 1998 (1998) (0)
- 491 Efficacy of oral tofacitinib in the treatment of lichen planopilaris (2018) (0)
- Contents vol. 219, 2009 (2009) (0)
- 786 A master regulator function of hairless in skin homeostasis and immune regulation (2020) (0)
- Newsletter ILDS No. 14 (2010) (0)
- nine Chapter fifty-four Basic Principles of Genetics (2012) (0)
- 522 Integrative analysis of gene expression data and rare copy number variants in alopecia areata (2017) (0)
- 660 Recapitulating T cell infiltration in psoriasis for patient-specific drug testing models (2019) (0)
- Plain language summaries in Simplified Chinese (2017) (0)
- Acknowledgments to Reviewers (1998) (0)
- 865 Conditional ablation of JAK-STAT5 signaling induces anagen hair growth (2017) (0)
- Acknowledgement to Referees for Dermatology 2009 (2009) (0)
- 909 Developing a 3D microfluidic model of immune-competent human skin using autologous cells (2017) (0)
- 526 Gut dysbiosis in alopecia areata patients reveals overabundance of firmicutes and under representation of bacteroides (2019) (0)
- 821 Pigmentation and autophagy in alopecia areata pathogenesis (2017) (0)
- ILDS Newsletter No. 12/2010 (2010) (0)
- 688 Efficacy of topical Vorinostat in the reversal of alopecia areata (2017) (0)
- Contents Vol. 14, 2001 (2001) (0)
- 1072 Promotion of hair growth in normal mouse skin and alopecia areata by topical treatment of HDAC inhibitors (2018) (0)
- 114 Blockade of Th2 and Th17 axes failed to prevent alopecia areata in C3H/HeJ grafted mice (2018) (0)
- An open-label study evaluating the efficacy of abatacept in alopecia areata supplementary data (2020) (0)
- Activation of EGF and FGF signaling in developing mouse skin inhibits hair follicle morphogenesis (2007) (0)
- Type I Punctate Palmoplantar Keratoderma: Identification and Refinement of a Locus for on Chromosome 15q22-24 and Evidence for Genetic Heterogeneity (2017) (0)
- Defining a Role for Hairless by Analytical Comparison of Differential Gene Expression (2005) (0)
- Ancestral patterns of recessive dystrophic epidermolysis bullosa mutations in Hispanic populations suggest sephardic ancestry (2021) (0)
- 616 Endoplasmic reticulum stress upregulates NKG2D ligands in the hair follicle (2017) (0)
- 427 Blockade of autophagy accelerates the development of alopecia areata (2019) (0)
- Montagna Symposium 2009: Genetic-epigenetic Basis of Skin Diseases. (2010) (0)
- Editorial (2004) (0)
- Immunogenic Catagen Initiates Alopecia Areata (2021) (0)
- 838 An eQTL in syntaxin17 (STX17) leads to disrupted melanogenesis in alopecia areata (2019) (0)
- Cloning of collagens of the cutaneous basement of membrane zone: Type VII and XVII (1994) (0)
- 487 Induction of T cell exhaustion by JAK1/3 inhibition in the treatment of alopecia areata (2018) (0)
- 522 Gut microbiota is required for the development of alopecia areata (2019) (0)
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias (2017) (0)
- PRE-READING MATERIALS (2016) (0)
- Molecular heterogeneity in erythropoietic protoporphyria: 10 mutations in the ferrochelatase gene (1998) (0)
- Newsletter No. 9/2009 (2009) (0)
- Phenotypic heterogeneity associated with haploinsufficiency mutations in the desmosomal plaque protein, desmoplakin (2000) (0)
- Abstract 1845: Enhancing the efficacy of antitumor antibodies with immune checkpoint inhibitors and targeted therapy in melanoma (2021) (0)
- 863 Molecular basis of hair follicle donor dominance in androgenetic alopecia and sexual dimorphism of the skin (2017) (0)
- Table. Pattern of Nail Dystrophy in R255X Heterozygous Subjects (2017) (0)
- Contents Vol. 223, 2011 (2012) (0)
- Generation of induced pluripotent stem cells from revertant mosaic keratinocytes (2014) (0)
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What Schools Are Affiliated With Angela M. Christiano?
Angela M. Christiano is affiliated with the following schools:
