Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5.
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White spotting in the domestic cat (Felis catus) maps near KIT on feline chromosome B1The original shaker-with-syndactylism mutation (sy) is a contiguous gene deletion syndrome.The mouse Clock mutation behaves as an antimorph and maps within the W19H deletion, distal of KitThe Wsh and Ph mutations affect the c-kit expression profile: c-kit misexpression in embryogenesis impairs melanogenesis in Wsh and Ph mutant mice.Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism.The molecular basis of human piebaldism.Structural analysis of chromosomal rearrangements associated with the developmental mutations Ph, W19H, and Rw on mouse chromosome 5.Control of melanocyte proliferation and differentiation in the mouse epidermis.Testicular development involves the spatiotemporal control of PDGFs and PDGF receptors gene expression and action.Rump white inversion in the mouse disrupts dipeptidyl aminopeptidase-like protein 6 and causes dysregulation of Kit expression.Embryonic mesoderm cells spread in response to platelet-derived growth factor and signaling by phosphatidylinositol 3-kinase.PDGFRβ regulates craniofacial development through homodimers and functional heterodimers with PDGFRαDeletion of the c-kit protooncogene in the human developmental defect piebald trait.Mouse as a model for multifactorial inheritance of neural tube defects.Pdgfrα functions in endothelial-derived cells to regulate neural crest cells and development of the great arteries.Oct-4 regulates alternative platelet-derived growth factor alpha receptor gene promoter in human embryonal carcinoma cells.Functional proteomics of signal transduction by membrane receptors.Sustained platelet-derived growth factor receptor alpha signaling in osteoblasts results in craniosynostosis by overactivating the phospholipase C-gamma pathway.PDGF-A and PDGFR-alpha regulate tooth formation via autocrine mechanism during mandibular morphogenesis in vitro.MAPK and PI3K Signaling: at the Crossroads of Neural Crest Development.D5Ucl1 and Els1 are closely linked to W on mouse chromosome 5 but lie distal to the W19H deletion.
P2860
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P2860
Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on June 1991
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Mouse platelet-derived growth ...... tch mutations on chromosome 5.
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Mouse platelet-derived growth ...... tch mutations on chromosome 5.
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type
label
Mouse platelet-derived growth ...... tch mutations on chromosome 5.
@en
Mouse platelet-derived growth ...... tch mutations on chromosome 5.
@nl
prefLabel
Mouse platelet-derived growth ...... tch mutations on chromosome 5.
@en
Mouse platelet-derived growth ...... tch mutations on chromosome 5.
@nl
P2093
P2860
P356
P1476
Mouse platelet-derived growth ...... tch mutations on chromosome 5.
@en
P2093
G G Choudhury
L Martinez
M F Seldin
M L Watson
P A Lalley
S Aaronson
S L Naylor
P2860
P304
P356
10.1073/PNAS.88.11.4811
P407
P577
1991-06-01T00:00:00Z