Andreas Kispert

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Andreas Kispert is affiliated with the following schools: University of Amsterdam, University of California, Berkeley, University of Oxford, Hannover Medical School, Stanford University

Andreas Kispert's AcademicInfluence.com Rankings

Andreas Kispert

Computer Science

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Computational Linguistics

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#2503

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Machine Learning

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#4545

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Artificial Intelligence

#4853

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#4916

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Computer Science

Andreas Kispert's Degrees

Bachelors Computer Science University of California, Berkeley

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Andreas Kispert'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

β‐catenin is a target for the ubiquitin–proteasome pathway (1997) (2372)
Female development in mammals is regulated by Wnt-4 signalling (1999) (1210)
beta-catenin is a target for the ubiquitin-proteasome pathway. (1997) (960)
A primary requirement for nodal in the formation and maintenance of the primitive streak in the mouse. (1994) (834)
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination (2003) (625)
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4 (2006) (560)
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry (2002) (515)
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible (2006) (511)
Wnt-4 is a mesenchymal signal for epithelial transformation of metanephric mesenchyme in the developing kidney. (1998) (510)
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure (2001) (475)
Wnt11 and Ret/Gdnf pathways cooperate in regulating ureteric branching during metanephric kidney development (2003) (473)
Liver Disintegration in the Mouse Embryo Caused by Deficiency in the RNA-editing Enzyme ADAR1* (2004) (408)
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin (2005) (379)
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis (2003) (352)
Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation. (2004) (347)
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness. (2011) (338)
Proteoglycans are required for maintenance of Wnt-11 expression in the ureter tips. (1996) (324)
The Brachyury gene encodes a novel DNA binding protein. (1993) (321)
The T protein encoded by Brachyury is a tissue‐specific transcription factor. (1995) (319)
CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs (2011) (314)
Okihiro syndrome is caused by SALL4 mutations. (2002) (307)
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. (2008) (303)
Formation of the Venous Pole of the Heart From an Nkx2–5–Negative Precursor Population Requires Tbx18 (2006) (292)
Formation of the Sinus Node Head and Differentiation of Sinus Node Myocardium Are Independently Regulated by Tbx18 and Tbx3 (2009) (279)
Tbx18 and the fate of epicardial progenitors (2009) (276)
Development of the Pacemaker Tissues of the Heart (2010) (269)
Brachyury is a target gene of the Wnt/β-catenin signaling pathway (2000) (266)
Mechanisms of T-box gene function in the developing heart. (2011) (236)
Cloning and expression analysis of the mouse T-box gene Tbx18 (2001) (235)
Immunohistochemical analysis of the Brachyury protein in wild-type and mutant mouse embryos. (1994) (232)
The T genes in embryogenesis. (1994) (222)
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects. (2009) (216)
Homologs of the mouse Brachyury gene are involved in the specification of posterior terminal structures in Drosophila, Tribolium, and Locusta. (1994) (204)
Tbx20 is essential for cardiac chamber differentiation and repression of Tbx2 (2005) (198)
Paracrine and autocrine mechanisms of apelin signaling govern embryonic and tumor angiogenesis. (2007) (188)
Identification of multipotent progenitors in the embryonic mouse kidney by a novel colony-forming assay (2006) (183)
A role for Pax-1 as a mediator of notochordal signals during the dorsoventral specification of vertebrae. (1993) (180)
GDNF induces branching and increased cell proliferation in the ureter of the mouse. (1997) (178)
The Tbx2+ Primary Myocardium of the Atrioventricular Canal Forms the Atrioventricular Node and the Base of the Left Ventricle (2009) (174)
The chick Brachyury gene: developmental expression pattern and response to axial induction by localized activin. (1995) (170)
The T-box transcription factor Tbx18 maintains the separation of anterior and posterior somite compartments. (2004) (165)
The sinus venosus progenitors separate and diversify from the first and second heart fields early in development. (2010) (159)
A protein kinase encoded by the t complex responder gene causes non-mendelian inheritance (1999) (155)
Brachyury is a target gene of the Wnt/beta-catenin signaling pathway. (2000) (153)
Notch Signaling Regulates Smooth Muscle Differentiation of Epicardium-Derived Cells (2011) (150)
The Brachyury gene encodes a novel DNA binding protein. (1993) (146)
Tbx18 regulates the development of the ureteral mesenchyme. (2006) (143)
sFRP‐2 is a target of the Wnt‐4 signaling pathway in the developing metanephric kidney (1998) (142)
Secreted Frizzled Related Protein 2 is a procollagen C proteinase enhancer with a role in myocardial infarction-associated fibrosis (2008) (142)
Developmental Origin, Growth, and Three-Dimensional Architecture of the Atrioventricular Conduction Axis of the Mouse Heart (2010) (133)
Cloning and expression analysis of the mouse T-box gene Tbx20 (2001) (131)
Wt1 and Epicardial Fate Mapping (2012) (131)
Tbx2 and Tbx3 induce atrioventricular myocardial development and endocardial cushion formation (2011) (123)
Tbx20 Interacts With Smads to Confine Tbx2 Expression to the Atrioventricular Canal (2009) (121)
The T-box transcription factor Tbx15 is required for skeletal development (2005) (120)
The prepattern transcription factor Irx3 directs nephron segment identity. (2007) (114)
SHH-N upregulates Sfrp2 to mediate its competitive interaction with WNT1 and WNT4 in the somitic mesoderm. (2000) (113)
Tbx3 promotes liver bud expansion during mouse development by suppression of cholangiocyte differentiation (2009) (113)
The paired homeobox gene Uncx4.1 specifies pedicles, transverse processes and proximal ribs of the vertebral column. (2000) (107)
Rescue of the tail defect of Brachyury mice. (1993) (107)
Expression patterns of Wnt genes in mouse gut development (2001) (106)
AHI1 is required for outer segment development and is a modifier for retinal degeneration in nephronophthisis (2010) (106)
Expression of Msgn1 in the presomitic mesoderm is controlled by synergism of WNT signalling and Tbx6 (2007) (103)
WNT signaling affects gene expression in the ventral diencephalon and pituitary gland growth (2008) (102)
Characterization of the Atypical MAPK ERK4 and Its Activation of the MAPK-activated Protein Kinase MK5* (2006) (98)
Transcriptional Repression by the T-box Proteins Tbx18 and Tbx15 Depends on Groucho Corepressors*♦ (2007) (93)
TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression. (2007) (91)
Sox9 is required for notochord maintenance in mice. (2006) (83)
Female Development in Mammals is Regulated by Wnt-4-Signaling (1999) (80)
An interacting network of T-box genes directs gene expression and fate in the zebrafish mesoderm (2003) (79)
Cloning and expression analysis of Sall4, the murine homologue of the gene mutated in Okihiro syndrome (2002) (78)
Left and right ventricular contributions to the formation of the interventricular septum in the mouse heart. (2006) (78)
The transcription factor GATA4 promotes myocardial regeneration in neonatal mice (2017) (76)
Wnt5a and Wnt11 regulate mammalian anterior-posterior axis elongation (2015) (74)
Wnt6 Is Expressed in Granulomatous Lesions of Mycobacterium tuberculosis–Infected Mice and Is Involved in Macrophage Differentiation and Proliferation (2013) (72)
Tbx18 expression demarcates multipotent precursor populations in the developing urogenital system but is exclusively required within the ureteric mesenchymal lineage to suppress a renal stromal fate. (2013) (71)
Regulation of neurotrophin-3 expression by epithelial-mesenchymal interactions: the role of Wnt factors. (1999) (71)
TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndrome. (2008) (70)
Down the tube of obstructive nephropathies: the importance of tissue interactions during ureter development. (2007) (69)
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development. (2015) (67)
A mouse gene of the paired-related homeobox class expressed in the caudal somite compartment and in the developing vertebral column, kidney and nervous system (1997) (67)
Inhibition of Sox2-dependent activation of Shh in the ventral diencephalon by Tbx3 is required for formation of the neurohypophysis (2013) (66)
Tbx15 controls skeletal muscle fibre-type determination and muscle metabolism (2015) (66)
Deafness in mice lacking the T-box transcription factor Tbx18 in otic fibrocytes (2008) (64)
Tbx2 Controls Lung Growth by Direct Repression of the Cell Cycle Inhibitor Genes Cdkn1a and Cdkn1b (2013) (64)
Renal-retinal ciliopathy gene Sdccag8 regulates DNA damage response signaling. (2014) (63)
Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism. (2006) (62)
Dach1, a vertebrate homologue of Drosophila dachshund, is expressed in the developing eye and ear of both chick and mouse and is regulated independently of Pax and Eya genes (2002) (61)
Embryonic expression of the murine homologue of SALL1, the gene mutated in Townes–Brocks syndrome (2001) (60)
Carboxypeptidase Z (CPZ) modulates Wnt signaling and regulates the development of skeletal elements in the chicken (2003) (59)
Tbx 20 is essential for cardiac chamber differentiation and repression of Tbx 2 (59)
Characterization of Pax-2 regulatory sequences that direct transgene expression in the Wolffian duct and its derivatives. (2001) (58)
Cystin localizes to primary cilia via membrane microdomains and a targeting motif. (2009) (58)
Neuronal expression and interaction with the synaptic protein CASK suggest a role for Neph1 and Neph2 in synaptogenesis (2006) (56)
Wnt6 Is Essential for Stromal Cell Proliferation During Decidualization in Mice1 (2013) (55)
Wnts differentially regulate colony growth and differentiation of chondrogenic rat calvaria cells. (2001) (52)
Hydroureternephrosis due to loss of Sox9-regulated smooth muscle cell differentiation of the ureteric mesenchyme. (2010) (52)
Tbx2 Terminates Shh/Fgf Signaling in the Developing Mouse Limb Bud by Direct Repression of Gremlin1 (2013) (50)
Nephrocystin: gene expression and sequence conservation between human, mouse, and Caenorhabditis elegans. (2000) (49)
Repression of Sox9 by Jag1 is continuously required to suppress the default chondrogenic fate of vascular smooth muscle cells. (2014) (49)
Wt1 and Retinoic Acid Signaling in the Subcoelomic Mesenchyme Control the Development of the Pleuropericardial Membranes and the Sinus Horns (2010) (49)
Loss of Sox9 in the periotic mesenchyme affects mesenchymal expansion and differentiation, and epithelial morphogenesis during cochlea development in the mouse. (2010) (48)
Analysis of TBX18 expression in chick embryos (2004) (48)
Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients. (2005) (48)
Sipl1 and Rbck1 Are Novel Eya1-Binding Proteins with a Role in Craniofacial Development (2010) (47)
Tbx2 and Tbx3 Act Downstream of Shh to Maintain Canonical Wnt Signaling during Branching Morphogenesis of the Murine Lung. (2016) (45)
Ureter growth and differentiation. (2014) (43)
Identification of a Wnt/β-Catenin Signaling Pathway in Human Thyroid Cells. (2001) (42)
Expression and requirement of T-box transcription factors Tbx2 and Tbx3 during secondary palate development in the mouse. (2009) (41)
Slit–Roundabout Signaling Regulates the Development of the Cardiac Systemic Venous Return and Pericardium (2013) (40)
Canonical Wnt signaling regulates smooth muscle precursor development in the mouse ureter (2012) (40)
Gene expression analysis identifies novel genes participating in early murine liver development and adult liver regeneration. (2006) (39)
T-box Protein Tbx18 Interacts with the Paired Box Protein Pax3 in the Development of the Paraxial Mesoderm* (2008) (39)
A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling. (2017) (39)
Serum-free differentiation of murine embryonic stem cells into alveolar type II epithelial cells. (2008) (39)
Genotype-phenotype correlations in PCD patients carrying DNAH5 mutations (2003) (38)
Epicardial function of canonical Wnt-, Hedgehog-, Fgfr1/2-, and Pdgfra-signalling. (2013) (38)
Upk3b Is Dispensable for Development and Integrity of Urothelium and Mesothelium (2014) (37)
MicroRNA-199a-5p inhibition enhances the liver repopulation ability of human embryonic stem cell-derived hepatic cells. (2015) (37)
Single-step purification and h.p.l.c. analysis of glutathione transferase 8-8 in rat tissues. (1989) (36)
Tbx18 function in epicardial development. (2012) (36)
GATA6 Promotes Angiogenic Function and Survival in Endothelial Cells by Suppression of Autocrine Transforming Growth Factor β/Activin Receptor-like Kinase 5 Signaling* (2010) (36)
Tbx15 Defines a Glycolytic Subpopulation and White Adipocyte Heterogeneity (2017) (34)
Growth differentiation factor 11 attenuates liver fibrosis via expansion of liver progenitor cells (2019) (34)
Comparative analysis of Neph gene expression in mouse and chicken development (2011) (33)
Inactivation of Sox9 in fibroblasts reduces cardiac fibrosis and inflammation. (2019) (33)
Sialic acid is a critical fetal defense against maternal complement attack (2018) (32)
Hepatocyte-specific suppression of microRNA-221-3p mitigates liver fibrosis. (2019) (30)
Purification and characterization of a labile rat glutathione transferase of the Mu class. (1989) (30)
Pax-2 regulatory sequences that direct transgene expression in the developing neural plate and external granule cell layer of the cerebellum. (1999) (30)
The Brachyury protein: A T-domain transcription factor (1995) (28)
Diversification of Cell Lineages in Ureter Development. (2017) (28)
A SHH-FOXF1-BMP4 signaling axis regulating growth and differentiation of epithelial and mesenchymal tissues in ureter development (2017) (28)
Wnt/&bgr;-Catenin Signaling Maintains the Mesenchymal Precursor Pool for Murine Sinus Horn Formation (2011) (28)
Cloning and expression analysis of the chick ortholog of TBX22, the gene mutated in X-linked cleft palate and ankyloglossia (2002) (27)
Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT) (2015) (27)
Partial Absence of Pleuropericardial Membranes in Tbx18- and Wt1-Deficient Mice (2012) (26)
Phenotypical Analysis of Atypical PKCs In Vivo Function Display a Compensatory System at Mouse Embryonic Day 7.5 (2013) (26)
Expression of fibulin-6 in failing hearts and its role for cardiac fibroblast migration. (2014) (25)
Impaired stria vascularis integrity upon loss of E-cadherin in basal cells. (2011) (24)
Canonical Wnt signaling regulates the proliferative expansion and differentiation of fibrocytes in the murine inner ear. (2014) (24)
Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations (2017) (24)
TBX2 and TBX3 act downstream of canonical WNT signaling in patterning and differentiation of the mouse ureteric mesenchyme (2018) (23)
GTPase domain driven dimerization of SEPT7 is dispensable for the critical role of septins in fibroblast cytokinesis (2016) (23)
Misexpression of Tbx18 in cardiac chambers of fetal mice interferes with chamber-specific developmental programs but does not induce a pacemaker-like gene signature. (2016) (21)
Tbx20, Smads, and the atrioventricular canal. (2010) (19)
Nephric duct insertion requires EphA4/EphA7 signaling from the pericloacal mesenchyme (2014) (19)
Regulation of otocyst patterning by Tbx2 and Tbx3 is required for inner ear morphogenesis in the mouse. (2021) (19)
BMP4 uses several different effector pathways to regulate proliferation and differentiation in the epithelial and mesenchymal tissue compartments of the developing mouse ureter (2017) (18)
Fgfr2 is required for the expansion of the early adrenocortical primordium (2015) (16)
The transcription factor Uncx4.1 acts in a short window of midbrain dopaminergic neuron differentiation (2012) (16)
TSHZ3 and SOX9 Regulate the Timing of Smooth Muscle Cell Differentiation in the Ureter by Reducing Myocardin Activity (2013) (16)
Promotion of gastrulation by maternal growth factor in cultured rabbit blastocysts (1995) (15)
Heparan Sulfate-Editing Extracellular Sulfatases Enhance Vascular Endothelial Growth Factor Bioavailability for Ischemic Heart Repair. (2019) (15)
Wnt11 Is Required for Oriented Migration of Dermogenic Progenitor Cells from the Dorsomedial Lip of the Avian Dermomyotome (2014) (14)
Identification of a Wnt/beta-catenin signaling pathway in human thyroid cells. (2001) (13)
Retinoic acid signaling maintains epithelial and mesenchymal progenitors in the developing mouse ureter (2017) (13)
Mesothelial mobilization in the developing lung and heart differs in timing, quantity, and pathway dependency. (2019) (12)
No muscle for a damaged heart: thymosin beta 4 treatment after myocardial infarction does not induce myocardial differentiation of epicardial cells. (2012) (12)
A 3D iPSC-differentiation model identifies interleukin-3 as a regulator of early human hematopoietic specification (2020) (12)
Eph/ephrin signaling in the kidney and lower urinary tract (2016) (10)
Establishment of the Visceral Embryonic Midline Is a Dynamic Process that Requires Bilaterally Symmetric BMP Signaling. (2016) (10)
Mutations in ACY 1 , the Gene Encoding Aminoacylase 1 , Cause a Novel Inborn Error of Metabolism (2007) (10)
A New Look at Tubulointerstitial Communication with Exosomes (2013) (9)
Wnt/Ctnnb1 signaling and the mesenchymal precursor pools of the heart. (2012) (9)
Tbx18 Regulates the Differentiation of Periductal Smooth Muscle Stroma and the Maintenance of Epithelial Integrity in the Prostate (2016) (8)
Tetrodotoxin-sensitive α-subunits of voltage-gated sodium channels are relevant for inhibition of cardiac sodium currents by local anesthetics (2016) (7)
Proteomic analysis identifies transcriptional cofactors and homeobox transcription factors as TBX18 binding proteins (2018) (7)
A distant downstream enhancer directs essential expression of Tbx18 in urogenital tissues. (2014) (7)
The mouse Rsk3 gene maps to the Leh66 elements carrying the t-complex responder Tcr (1999) (7)
TBX2-positive cells represent a multi-potent mesenchymal progenitor pool in the developing lung (2019) (7)
WNT6/ACC2-induced storage of triacylglycerols in macrophages is exploited by Mycobacterium tuberculosis. (2021) (6)
Delayed onset of smooth muscle cell differentiation leads to hydroureter formation in mice with conditional loss of the zinc finger transcription factor gene Gata2 in the ureteric mesenchyme (2019) (6)
Epicardial Lineages (2013) (6)
Loss of Anks6 leads to YAP deficiency and liver abnormalities. (2020) (6)
Dexamethasone improves therapeutic outcomes in a preclinical bacterial epididymitis mouse model. (2019) (6)
Lack of Genetic Interaction between Tbx18 and Tbx2/Tbx20 in Mouse Epicardial Development (2016) (6)
Tbx2 and Tbx3 induce atrioventricular myocardial development and endocardial cushion formation (2011) (6)
Combined genomic and proteomic approaches reveal DNA binding sites and interaction partners of TBX2 in the developing lung (2021) (5)
Rare heterozygous GDF6 variants in patients with renal anomalies (2020) (5)
Expansion of the renal capsular stroma, ureteric bud branching defects and cryptorchidism in mice with Wilms tumor 1 gene deletion in the stromal compartment of the developing kidney (2020) (5)
WNT6-ACC2-induced accumulation of triacylglycerol rich lipid droplets is exploited by M. tuberculosis (2020) (3)
T-Box Genes in the Kidney and Urinary Tract. (2017) (3)
Proteomic analysis identifies ZMYM2 as endogenous binding partner of TBX18 protein in 293 and A549 cells. (2021) (3)
Gne deletion in mice leads to lethal intracerebral hemorrhage during embryonic development. (2021) (3)
FGFR2 signaling enhances the SHH-BMP4 signaling axis in early ureter development. (2022) (3)
Inflammation-like changes in the urothelium of Lifr-deficient mice and LIFR-haploinsufficient humans with urinary tract anomalies. (2020) (2)
CHAPTER 11 – Introduction to Early Mouse Development (2004) (2)
The transcription factor GATA4 promotes myocardial regeneration in neonatal mice (2019) (2)
Generation of hiPSC-derived low threshold mechanoreceptors containing axonal termini resembling bulbous sensory nerve endings and expressing Piezo1 and Piezo2. (2021) (2)
Notch signaling is a novel regulator of visceral smooth muscle cell differentiation in the murine ureter. (2022) (1)
Redundant function of Wnt5a and Wnt11 in somitogenesis and anteroposterior axis elongation (2008) (1)
09-P043 Tbx3 promotes liver bud expansion during mouse development by suppression of cholangiocyte differentiation (2009) (1)
S100A1 expression characterizes terminally differentiated superficial cells in the urothelium of the murine bladder and ureter (2022) (1)
patterns during cardiac development Three-dimensional reconstruction of gene expression (2015) (1)
The transcription factor Uncx4.1 acts in a short window of midbrain dopaminergic neuron differentiation (2012) (1)
TBX2 specifies and maintains inner hair and supporting cell fate in the Organ of Corti (2022) (1)
GATA6 is a crucial factor for Myocd expression in the visceral smooth muscle cell differentiation program of the murine ureter. (2022) (1)
UvA-DARE ( Digital Academic Repository ) The Tbx 2 ( + ) Primary Myocardium of the Atrioventricular Canal Forms the Atrioventricular Node and the Base of the Left Ventricle (2009) (0)
Tetrodotoxin-sensitive α-subunits of voltage-gated sodium channels are relevant for inhibition of cardiac sodium currents by local anesthetics (2016) (0)
Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs (2022) (0)
Purification andcharacterization ofalabile ratglutathione transferase oftheMu class (1989) (0)
Corrigendum to: 'Hepatocyte-specific suppression of microRNA-221-3p mitigates liver fibrosis' [J Hepatol (2019) 722-734]. (2022) (0)
Correction: Tbx18 Regulates the Differentiation of Periductal Smooth Muscle Stroma and the Maintenance of Epithelial Integrity in the Prostate (2016) (0)
Subject Index Vol. 98, 2002 (2003) (0)
Ardem Patapoutian Interactions : The Role of Wnt Factors Regulation of Neurotrophin-3 Expression by Epithelial-Mesenchymal (2011) (0)
Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT) (2015) (0)
Differentiation of embryonic stem cells into type-II pneumocytes (2006) (0)
Mutations in NRIP 1 cause dominant urinary tract malformations via dysregulation of retinoic acid signaling (2017) (0)
Interplay between Tbx20, Tbx2/Tbx3 and Bmp/Smad- signaling controls compartmentalization of the developing heart tube into working chambers and the atrioventricular canal (2009) (0)
Chapter 2.1 – Early Mouse Development (2012) (0)
Brief UltraRapid Communication Wt1 and Epicardial Fate Mapping (2012) (0)
Contents continued (2001) (0)
Contents Vol. 98, 2002 (2003) (0)
Permissive ureter specification by TBX18-mediated repression of metanephric gene expression. (2023) (0)
Wnt genes affect patterning of the ventral diencephalon and pituitary gland growth (2006) (0)
Mesenchymal FGFR1 and FGFR2 control patterning of the ureteric mesenchyme by balancing SHH and BMP4 signaling. (2022) (0)
A large number of human genetic disorders and of mouse mutants as well as embryological manipulations in the chick embryo have shed some light on the genetic control of early somite patterning and differentiation, and on cell lineage (2000) (0)
Herrmann A mouse gene of the paired-related homeobox class expressed in the caudal somite compartment and in the developing vertebral column , kidney and nervous system (0)
Differentiation and Proliferation and Is Involved in Macrophage Infected Mice - Mycobacterium tuberculosis of Wnt6 Is Expressed in Granulomatous Lesions (2013) (0)
Inhibition of ependymal flow during brain development: A novel mechanism for hydrocephalus formation (2005) (0)
Editorial board members (2007) (0)
NPHP3 expression in ciliated neural precursor cells of the cerebellum suggests a specific function of nephrocystin-3 for cerebellar development (2004) (0)
Heterozygous variants in the DVL2 interaction region of DACT1 cause CAKUT and features of Townes–Brocks syndrome 2 (2022) (0)
Comparative analysis of Neph gene expression in mouse and chicken development (2011) (0)
Retinoic acid signaling maintains epithelial and mesenchymal progenitors in the developing mouse ureter (2017) (0)

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What Schools Are Affiliated With Andreas Kispert?

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