Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome
about
Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disordersWNT5A mutations in patients with autosomal dominant Robinow syndromeIdentification of Ror2 as a hypoxia-inducible factor target in von Hippel-Lindau-associated renal cell carcinomaRor2, a developmentally regulated kinase, promotes tumor growth potential in renal cell carcinomaDistinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)Molecular basis of cleft palates in miceThe dual role of the novel Wnt receptor tyrosine kinase, ROR2, in human carcinogenesismicroRNA regulation of Wnt signaling pathways in development and diseaseProspective isolation of human embryonic stem cell-derived cardiovascular progenitors that integrate into human fetal heart tissueDysregulation of Wnt inhibitory factor 1 (Wif1) expression resulted in aberrant Wnt-β-catenin signaling and cell death of the cloaca endoderm, and anorectal malformations.Prickle1 is necessary for the caudal migration of murine facial branchiomotor neurons.Wnt5a regulates growth, patterning, and odontoblast differentiation of developing mouse tooth.Expression of type XXIII collagen mRNA and protein.Ror receptor tyrosine kinases: orphans no more.Planar cell polarity signaling in craniofacial development.ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian populationPartitioning the heart: mechanisms of cardiac septation and valve developmentTargeting ROR1 identifies new treatment strategies in hematological cancers.Molecular signaling along the anterior-posterior axis of early palate development.Development of the external genitalia: conserved and divergent mechanisms of appendage patterning.The functions and possible significance of Kremen as the gatekeeper of Wnt signalling in development and pathology.Analysis of PRICKLE1 in human cleft palate and mouse development demonstrates rare and common variants involved in human malformations.Alternative Wnt pathways and receptors.When hormone defects cannot explain it: malformative disorders of sex development.Prickle1 stunts limb growth through alteration of cell polarity and gene expressionA Novel Role for the BMP Antagonist Noggin in Sensitizing Cells to Non-canonical Wnt-5a/Ror2/Disheveled Pathway ActivationSignaling pathways and tissue interactions in neural plate border formation.Craniofacial and intraoral phenotype of Robinow syndrome forms.Abnormal WNT5A Signaling Causes Mandibular Hypoplasia in Robinow Syndrome.Wnt5a regulates directional cell migration and cell proliferation via Ror2-mediated noncanonical pathway in mammalian palate developmentIsolation of primitive endoderm, mesoderm, vascular endothelial and trophoblast progenitors from human pluripotent stem cells.The receptor tyrosine kinase Ror2 associates with and is activated by casein kinase Iepsilon.The Wnt5a Receptor, Receptor Tyrosine Kinase-Like Orphan Receptor 2, Is a Predictive Cell Surface Marker of Human Mesenchymal Stem Cells with an Enhanced Capacity for Chondrogenic Differentiation.WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome.Mathematical analysis of mandibular morphogenesis by micro-CT-based mouse and alizarin red S-stained-based human studies during development.WNT5A and Its Receptors in the Bone-Cancer Dialogue.Essential role of Wnt5a-Ror1/Ror2 signaling in metanephric mesenchyme and ureteric bud formation.Role of WNT5A receptors FZD5 and RYK in prostate cancer cells.
P2860
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P2860
Ror2 knockout mouse as a model for the developmental pathology of autosomal recessive Robinow syndrome
description
2004 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2004
@ast
im Februar 2004 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2004/02/01)
@sk
vědecký článek publikovaný v roce 2004
@cs
wetenschappelijk artikel (gepubliceerd op 2004/02/01)
@nl
наукова стаття, опублікована в лютому 2004
@uk
مقالة علمية (نشرت في فبراير 2004)
@ar
name
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@ast
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@en
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@nl
type
label
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@ast
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@en
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@nl
prefLabel
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@ast
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@en
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@nl
P2093
P2860
P356
P1476
Ror2 knockout mouse as a model ...... mal recessive Robinow syndrome
@en
P2093
Britta Trepczik
Georg C. Schwabe
Kathrin Süring
Norbert Brieske
Paul T. Sharpe
Stefan Mundlos
Yasuhiro Minami
P2860
P304
P356
10.1002/DVDY.10466
P577
2004-02-01T00:00:00Z