A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
about
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humansBrain and Retinal Pericytes: Origin, Function and RoleFunctional Characterization of Germline Mutations in PDGFB and PDGFRB in Primary Familial Brain CalcificationNotch3 establishes brain vascular integrity by regulating pericyte number.From pathobiology to the targeting of pericytes for the treatment of diabetic retinopathyNOTCH3 regulates stem-to-mural cell differentiation in infantile hemangioma.The Novel Pathogenesis of Retinopathy Mediated by Multiple RTK Signals is Uncovered in Newly Developed Mouse Model.
P2860
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P2860
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
description
2013 nî lūn-bûn
@nan
2013 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
@ast
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
@en
type
label
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
@ast
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
@en
prefLabel
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
@ast
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
@en
P2093
P2860
P356
P1476
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathy.
@en
P2093
Alan W Hart
Margaret Keighren
Richard L Mort
Russell Joynson
Sara Wells
Shalini Jadeja
P2860
P304
P356
10.1167/IOVS.12-11125
P407
P577
2013-05-01T00:00:00Z