Bruno Reversade
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American geneticist
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Biology
Bruno Reversade's Degrees
- PhD Genetics Stanford University
Why Is Bruno Reversade Influential?
(Suggest an Edit or Addition)According to Wikipedia, Bruno Reversade is an American human geneticist and developmental biologist . He is a Director of the Institute of Molecular and Cellular Biology and the Genome Institute of Singapore at A*STAR and holds several faculty positions at other universities. Reversade is known for identifying mutated genes that cause Mendelian diseases, for his research on the genetics of identical twins and for the characterizations of novel hormones.
Bruno Reversade'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
- Connective-tissue growth factor (CTGF) modulates cell signalling by BMP and TGF-β (2002) (565)
- Connective-tissue growth factor (CTGF) modulates cell signalling by BMP and TGF-beta. (2002) (410)
- ELABELA: a hormone essential for heart development signals via the apelin receptor. (2013) (351)
- Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report (2011) (271)
- Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation (2016) (260)
- Regulation of ADMP and BMP2/4/7 at Opposite Embryonic Poles Generates a Self-Regulating Morphogenetic Field (2005) (246)
- Mutations in PYCR1 cause cutis laxa with progeroid features (2009) (228)
- Embryonic Dorsal-Ventral Signaling: Secreted Frizzled-Related Proteins as Inhibitors of Tolloid Proteinases (2006) (221)
- Proteolytic cleavage of Chordin as a switch for the dual activities of Twisted gastrulation in BMP signaling. (2001) (156)
- Multiple self-healing squamous epithelioma is caused by a disease-specific spectrum of mutations in TGFBR1 (2011) (152)
- Default neural induction: neuralization of dissociated Xenopus cells is mediated by Ras/MAPK activation. (2005) (152)
- ELABELA deficiency promotes preeclampsia and cardiovascular malformations in mice (2017) (146)
- Depletion of Bmp2, Bmp4, Bmp7 and Spemann organizer signals induces massive brain formation in Xenopus embryos (2005) (143)
- Chordin is required for the Spemann organizer transplantation phenomenon in Xenopus embryos. (2003) (140)
- ELABELA Is an Endogenous Growth Factor that Sustains hESC Self-Renewal via the PI3K/AKT Pathway. (2015) (134)
- RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6 (2018) (116)
- Human DPP9 represses NLRP1 inflammasome and protects against autoinflammatory diseases via both peptidase activity and FIIND domain binding (2018) (114)
- Enteroviral 3C protease activates the human NLRP1 inflammasome in airway epithelia (2020) (98)
- ELABELA-APJ axis protects from pressure overload heart failure and angiotensin II-induced cardiac damage (2017) (96)
- The hormonal peptide Elabela guides angioblasts to the midline during vasculogenesis (2015) (95)
- Discovery and Structure-Activity Relationship of a Bioactive Fragment of ELABELA that Modulates Vascular and Cardiac Functions. (2016) (93)
- De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development (2017) (88)
- Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signaling. (2010) (86)
- Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility. (2016) (83)
- Sirenomelia in Bmp7 and Tsg compound mutant mice: requirement for Bmp signaling in the development of ventral posterior mesoderm (2005) (82)
- Katanin p80 Regulates Human Cortical Development by Limiting Centriole and Cilia Number (2014) (81)
- Genome-wide CRISPR-Cas9 Screen Identifies Leukemia-Specific Dependence on a Pre-mRNA Metabolic Pathway Regulated by DCPS. (2018) (81)
- Alternative Progenitor Cells Compensate to Rebuild the Coronary Vasculature in Elabela- and Apj-Deficient Hearts. (2017) (81)
- The opposing homeobox genes Goosecoid and Vent1/2 self-regulate Xenopus patterning (2007) (76)
- De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations. (2016) (75)
- The pro-BMP activity of Twisted gastrulation is independent of BMP binding (2003) (75)
- Fifteen years of research on oral–facial–digital syndromes: from 1 to 16 causal genes (2017) (72)
- C5orf42 is the major gene responsible for OFD syndrome type VI (2014) (71)
- Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma (2012) (69)
- Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1 (2012) (65)
- Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa. (2015) (64)
- Gmnc Is a Master Regulator of the Multiciliated Cell Differentiation Program (2015) (63)
- Homozygous NLRP1 gain-of-function mutation in siblings with a syndromic form of recurrent respiratory papillomatosis (2019) (62)
- Gene expression profiles in normal and Otx2-/- early gastrulating mouse embryos. (2000) (60)
- Mitochondrial peptide BRAWNIN is essential for vertebrate respiratory complex III assembly (2020) (60)
- Metabolic pathway analyses identify proline biosynthesis pathway as a promoter of liver tumorigenesis. (2019) (48)
- Long-Term Culture of Self-renewing Pancreatic Progenitors Derived from Human Pluripotent Stem Cells (2017) (47)
- Structural basis of RIP2 activation and signaling (2018) (43)
- A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability (2018) (40)
- KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis (2017) (39)
- SMCHD1 is involved in de novo methylation of the DUX4-encoding D4Z4 macrosatellite (2019) (35)
- Structural basis for distinct inflammasome complex assembly by human NLRP1 and CARD8 (2020) (33)
- Quantitative imaging reveals real-time Pou5f3–Nanog complexes driving dorsoventral mesendoderm patterning in zebrafish (2016) (32)
- A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome (2016) (32)
- Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease (2021) (30)
- Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects (2015) (28)
- The Apelin receptor enhances Nodal/TGFβ signaling to ensure proper cardiac development (2016) (27)
- FSHD2- and BAMS-associated mutations confer opposing effects on SMCHD1 function (2018) (27)
- Somatic genetic rescue of a germline ribosome assembly defect (2021) (25)
- Elabela Antagonizes Intrarenal Renin-Angiotensin System to Lower Blood Pressure and Protects Against Renal Injury. (2020) (25)
- Katanin p80, NuMA and cytoplasmic dynein cooperate to control microtubule dynamics (2017) (25)
- Loss of PYCR2 Causes Neurodegeneration by Increasing Cerebral Glycine Levels via SHMT2 (2020) (24)
- Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology (2020) (24)
- Human NLRP1 is a sensor of pathogenic coronavirus 3CL proteases in lung epithelial cells (2022) (23)
- CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental Delays. (2017) (23)
- Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy (2020) (23)
- Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization (2016) (21)
- Incidentalome from Genomic Sequencing: A Barrier to Personalized Medicine? (2016) (21)
- Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome. (2018) (20)
- Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling. (2016) (20)
- IL11 is elevated in systemic sclerosis and IL11-dependent ERK signalling underlies TGFβ-mediated activation of dermal fibroblasts (2021) (20)
- Direct identification of A-to-I editing sites with nanopore native RNA sequencing (2022) (18)
- Next‐generation sequencing in a series of 80 fetuses with complex cardiac malformations and/or heterotaxy (2020) (18)
- Nuclear-localized Asunder regulates cytoplasmic dynein localization via its role in the Integrator complex (2013) (18)
- Human Asunder promotes dynein recruitment and centrosomal tethering to the nucleus at mitotic entry (2012) (18)
- Characterization of a cDNA encoding a novel band 4.1-like protein in zebrafish. (1997) (18)
- Discriminative Features in Three Autosomal Recessive Cutis Laxa Syndromes: Cutis Laxa IIA, Cutis Laxa IIB, and Geroderma Osteoplastica (2017) (17)
- The snRNA-processing complex, Integrator, is required for ciliogenesis and dynein recruitment to the nuclear envelope via distinct mechanisms (2013) (17)
- ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis. (2017) (16)
- Multiple Self-Healing Palmoplantar Carcinoma: A Familial Predisposition to Skin Cancer with Primary Palmoplantar and Conjunctival Lesions (2014) (16)
- A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signaling (2020) (16)
- Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita. (2017) (16)
- Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction. (2020) (15)
- Identical twins carry a persistent epigenetic signature of early genome programming (2021) (15)
- Optimal histone H3 to linker histone H1 chromatin ratio is vital for mesodermal competence in Xenopus (2013) (14)
- R-spondin signalling is essential for the maintenance and differentiation of mouse nephron progenitors (2020) (13)
- Homozygous Null TBX4 Mutations Lead to Posterior Amelia with Pelvic and Pulmonary Hypoplasia. (2019) (12)
- R-SPONDIN2+ Mesenchymal Cells Form the Bud Tip Progenitor Niche During Human Lung Development (2021) (11)
- Dominant-negative NFKBIA mutation promotes IL-1β production causing hepatic disease with severe immunodeficiency. (2020) (11)
- A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion. (2021) (10)
- Publisher Correction: Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates (2021) (10)
- Congenital insensitivity to pain with anhidrosis syndrome: A series from Jordan (2019) (10)
- A Micropatterned Human‐Specific Neuroepithelial Tissue for Modeling Gene and Drug‐Induced Neurodevelopmental Defects (2021) (9)
- Definition of the phenotypic spectrum of Temtamy preaxial brachydactyly syndrome associated with autosomal recessive CHYS1 mutations (2012) (8)
- Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features (2019) (8)
- SMCHD 1 is involved in de novo methylation of the DUX 4-encoding D 4 Z 4 macrosatellite (2019) (7)
- Intellectual disability, muscle weakness and characteristic face in three siblings: A newly described recessive syndrome mapping to 3p24.3–p25.3 (2015) (7)
- Leveraging interacting signaling pathways to robustly improve the quality and yield of human pluripotent stem cell-derived hepatoblasts and hepatocytes (2022) (7)
- Mutation in TWINKLE in a Large Iranian Family with Progressive External Ophthalmoplegia, Myopathy, Dysphagia and Dysphonia, and Behavior Change. (2016) (7)
- Heterozygous missense variant in EIF6 gene: A novel form of Shwachman-Diamond syndrome? (2020) (7)
- Bone matrix hypermineralization associated with low bone turnover in a case of Nasu-Hakola disease. (2019) (7)
- Biallelic ZNFX1 variants are associated with a spectrum of immuno‐hematological abnormalities (2021) (7)
- Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen storage-associated mitochondriopathy. (2021) (6)
- DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signaling (2021) (6)
- Cenani-Lenz syndactyly syndrome - a case report of a family with isolated syndactyly (2018) (6)
- INTS13 Mutations Causing a Developmental Ciliopathy Disrupt Integrator Complex Assembly (2020) (5)
- Gmnc Is a Master Regulator of the Multiciliated Cell Differentiation Program (2017) (5)
- Congenital posterior cervical spine malformation due to biallelic c.240‐4T>G RIPPLY2 variant: A discrete entity (2020) (4)
- Leveraging complex interactions between signaling pathways involved in liver development to robustly improve the maturity and yield of pluripotent stem cell-derived hepatocytes (2020) (4)
- SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease (2021) (3)
- A novel nonsense ATP2C1 mutation causes Hailey-Hailey disease in a Tunisian family (2018) (3)
- Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 system. (2021) (3)
- Huriez syndrome caused by a large deletion that abrogates the skin‐specific isoform of SMARCAD1 (2021) (3)
- C10orf99/GPR15L Regulates Proinflammatory Response of Keratinocytes and Barrier Formation of the Skin (2022) (3)
- Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis (2022) (3)
- MATTHEW-WOOD SYNDROME: A CASE WITH DEXTROCARDIA AND STREAK GONADS. (2016) (3)
- Mitchell-Riley syndrome iPSC exhibit reduced pancreatic endoderm differentiation due to an RFX6 mutation. (2020) (3)
- AKT Signaling Modifies the Balance between Cell Proliferation and Migration in Neural Crest Cells from Patients Affected with Bosma Arhinia and Microphthalmia Syndrome (2021) (3)
- INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex (2022) (3)
- Author response: The Apelin receptor enhances Nodal/TGFβ signaling to ensure proper cardiac development (2016) (2)
- Ermin deficiency leads to compromised myelin, inflammatory milieu, and susceptibility to demyelinating insult (2022) (2)
- A GLI3 variant leading to polydactyly in heterozygotes and Pallister‐Hall‐like syndrome in a homozygote (2020) (2)
- Cloning and functional study of Nanog in zebrafish (2011) (2)
- Heterozygous Missense Variant in EIF6 gene: a novel form of Shwachman‐Diamond Syndrome? (2021) (2)
- Mitchell-Riley syndrome iPSC exhibit reduced pancreatic endoderm differentiation due to an RFX6 mutation. (2020) (2)
- Huriez syndrome: Additional pathogenic variants supporting allelism to SMARCAD syndrome (2022) (2)
- Author response: The hormonal peptide Elabela guides angioblasts to the midline during vasculogenesis (2015) (2)
- Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders (2014) (2)
- Structural basis for distinct inflammasome complex assembly by human NLRP1 and CARD8 (2021) (2)
- Increased Endoplasmic Reticulum Stress in patients with Congenital Liver Fibrosis caused by germline mutations in a Protein Disulfide Isomerase (2017) (1)
- Bi-allelic loss-of-function variants in TMEM147 cause moderate to profound intellectual disability with facial dysmorphism and pseudo-Pelger-Huët anomaly (2022) (1)
- Generation of four H1 hESC sublines carrying a hemizygous knock-out/mutant MECP2. (2019) (1)
- A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings. (2022) (1)
- Peptide hormone ELABELA that causes pre-eclampsia-like symptoms in knockout mice enhances human trophoblast invasion (2017) (1)
- Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6 (2018) (1)
- Author response: R-spondin signalling is essential for the maintenance and differentiation of mouse nephron progenitors (2020) (1)
- 5922A novel APJ ligand, ELABELA/Apela/Toddler, protects from pressure overload- and Angiotensin II-induced cardiac hypertrophy and fibrosis (2017) (1)
- HOX epimutations driven by maternal SMCHD1/LRIF1 haploinsufficiency trigger homeotic transformations in genetically wildtype offspring (2022) (1)
- University of Groningen De Novo Loss-of-Function Mutations in USP 9 X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations (2018) (1)
- SMCHD1 variants may induce variegated expression in Facio Scapulo Humeral Dystophy and Bosma Arhinia and microphtalmia syndrome (2021) (1)
- Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates (2021) (1)
- UGDH germline loss-of-function mutations cause epilepsy and global developmental delay (2017) (1)
- Mitochondrial peptide BRAWNIN is essential for vertebrate respiratory complex III assembly (2020) (1)
- Ermin deficiency as an inside-out model of inflammatory dysmyelination (2020) (1)
- RAF1 deficiency causes a lethal syndrome that underscores RTK signaling during embryogenesis. (2023) (0)
- A Progeroid Syndrome Caused by RAF1 deficiency Underscores the importance of RTK signaling for Human Development (2022) (0)
- 424 C10orf99 governs keratinocyte inflammatory response and barrier formation of the skin (2022) (0)
- P98. Raiders of the lost FRINGE (2010) (0)
- 13462 Elucidating the role of innate immunity involving interleukin-1 cytokines and inflammasome signaling pathways in the pathogenesis of psoriasis (2020) (0)
- Deciphering the consequence of deep intronic variants: a progeroid syndrome caused by a TAPT1 mutation is revealed by combined RNA/SI-NET sequencing (2022) (0)
- Schwartz-Jampel Syndrome (SJS1), Type 1 a Novel Variant in the HSPG2 Gene (2018) (0)
- Omics profiling identifies MAPK/ERK pathway as a gatekeeper of nephron progenitor metabolism (2021) (0)
- Title Long-Term Culture of Self-renewing PancreaticProgenitors Derived from Human Pluripotent Stem Cells (2018) (0)
- 06-P037 Dubowitz syndrome maps to chromosome 12 within an interval of 70 genes (2009) (0)
- Inactivation of DRG1, encoding a translation factor GTPase, causes a Recessive Neurodevelopmental Disorder (2022) (0)
- Abstract P111: ELABELA Antagonizes Intrarenal Renin to Lower Blood Pressure and Protect Against Renal Injury (2018) (0)
- Structural basis of RIP2 activation and signaling (2018) (0)
- 06-P018 Skin development and aging are under the control of the proline metabolic pathway (2009) (0)
- Loss of C2orf69 defines a fatal auto-inflammatory mitochondriopathy in Humans and Zebrafish (2021) (0)
- A deleterious recessive mutation in NUAK2 causes absence of brain in humans (2017) (0)
- Reto: A Novel Secreted Peptide in the Skin (2017) (0)
- Direct cleavage of human NLRP1 by enteroviral 3C protease triggers inflammasome activation in airway epithelium (2020) (0)
- Mutations in Pycr1 cause progeroid changes in skin and bone due to reduced mitochondrial stress resistance (2010) (0)
- Requirement of Goosecoid in early Xenopus development: A loss-of-function study (2007) (0)
- 06-P053 ENT3, mutated in H syndrome, is required for proper heart formation (2009) (0)
- 05-P010 Histone variant H3.3 is required for Xenopus embryonic development (2009) (0)
- Loss-of-function mutations in Carboxypeptidase D cause a new syndrome with lymphedema and sensorineural hearing loss (2017) (0)
- Author Correction: Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology (2020) (0)
- Omics profiling identifies the regulatory functions of the MAPK/ERK pathway in nephron progenitor metabolism (2022) (0)
- Differentiation of iPS-RPE cells from a patient with clinical anophthalmia (2013) (0)
- Identifying the Alternative Receptor of ELABELA in hESCs (2017) (0)
- P106. Congenital hypertelorism and osteopenia: A novel autosomal recessive disease (2010) (0)
- Human NLRP1 Is a Sensor of 3CL Proteases from Pathogenic Coronaviruses in Lung Epithelial Cells (2021) (0)
- The Organization Committee of the Spinoza Chair, set up by the Amsterdam University Association on behalf of the Faculty of Medicine of the University of Amsterdam, has awarded the Spinoza Chair to (2015) (0)
- A unique secreted peptide regulates early embryogenesis in vertebrates (2011) (0)
- Isogenic iPSC-derived models of disease (2013) (0)
- Publisher Correction: Somatic genetic rescue of a germline ribosome assembly defect (2022) (0)
- Stem Cell Society Singapore Symposium 2013 (2013) (0)
- Abstract LB-245: Loss of function of the TGFβRI receptor leads to the spontaneously regressing squamous carcinoma condition, multiple self-healing squamous epithelioma (Ferguson-Smith disease) (2011) (0)
- 06-P029 Congenital hypertelorism & osteopenia, a novel autosomal recessive disease of development (2009) (0)
- University of Groningen Recurrent De Novo Mutations Affecting Residue Arg1 38 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa Fischer-Zirnsak, (0)
- Author response: A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability (2018) (0)
- DPP9 is an endogenous and direct inhibitor of the NLRP1 inflammasome that guards against human auto-inflammatory diseases (2018) (0)
- MUTANT SMCHD1 FOR THERAPY (2018) (0)
- Genome-Wide CRISPR/Cas9 Screen Reveals That the Dcps Scavenger Decapping Enzyme Is Essential for AML Cell Survival (2017) (0)
- A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI‐NET sequencing (2023) (0)
- 901 Inflammasome signaling and translocation of apoptotic speck-like protein containing a caspase activation and recruitment domain (ASC) in psoriatic keratinocytes (2018) (0)
- To see, or not to see: In the eye of Retinol and STRA6 signaling (2011) (0)
- Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features (2022) (0)
- Ischemia-driven exosome release of human iPSC-CM-derived cardiomyocytes increase viability of endothelial cells via pro-survival factors BENCH Dipeptidyl peptidase-4 inhibitor markedly enhances the cardioprotective efficacy of Sodium-glucose cotransporter-2 inhibitor in pre-diabetic rats with cardiac (0)
- Paracrine and autocrine R-spondin signalling is essential for the maintenance and differentiation of renal stem cells (2019) (0)
- Editorial overview: Cilia in development and disease. (2019) (0)
- Hamamy syndrome: Deciphering the role of IRX5 transcription factor in the regulation of human cardiac electrical conduction (2017) (0)
- Neurodevelopmental Defects: A Micropatterned Human‐Specific Neuroepithelial Tissue for Modeling Gene and Drug‐Induced Neurodevelopmental Defects (Adv. Sci. 5/2021) (2021) (0)
- Building a nose: Mutations in an epigenetic regulator cause congenital arhinia (2017) (0)
- P97. Loss of CHSY1, a novel FRINGE enzyme, causes syndromic brachydactyly via increased NOTCH signaling (2010) (0)
- TOUT-DE-TRAVERS (TDT): A novel protease mutated in patients with heterotaxy drives left-right asymmetry upstream of Nodal signalling (2017) (0)
- RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation (2021) (0)
- Publisher Correction: Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates (2022) (0)
- 578Hamamy syndrome: Deciphering the role of IRX5 transcription factor in the regulation of human cardiac electrical conduction (2017) (0)
- PYCR2 Protects from Neurodegeneration by Controlling Oligodendrocyte Maturation and Glycinemia through SHMT2 (2017) (0)
- Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6 (2018) (0)
- A Micropatterned Human‐Specific Neuroepithelial Tissue for Modeling Gene and Drug‐Induced Neurodevelopmental Defects (2021) (0)
- Remodelling and cardioprotection 1247 (0)
- C5orf42 is the major gene responsible for OFD syndrome type VI (2013) (0)
- Loss of C2orf69 defines a fatal autoinflammatory syndrome in humans and zebrafish that evokes a glycogen-storage-associated mitochondriopathy. (2021) (0)
- BRAWNIN: A sORF-encoded Peptide Essential for Vertebrate Mitochondrial Complex III Assembly (2020) (0)
- Mutated NS1-BP causes segmental premature ageing of skin and neural lineages (2017) (0)
- The Opto-inflammasome in zebrafish: a tool to study cell and tissue responses to speck formation and cell death (2022) (0)
- 176 C10orf99/2610528A11Rik induces keratinocyte proinflammatory response and regulates lipid metabolism and barrier formation of the skin (2022) (0)
- RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6 (2018) (0)
- Author response: Quantitative imaging reveals real-time Pou5f3–Nanog complexes driving dorsoventral mesendoderm patterning in zebrafish (2016) (0)
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