RAX and anophthalmia in humans: evidence of brain anomalies.
about
Activation of Wnt/ß-catenin signaling in ESC promotes rostral forebrain differentiation in vitro.Conserved genetic pathways associated with microphthalmia, anophthalmia, and coloboma.Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations.Essential function of the transcription factor Rax in the early patterning of the mammalian hypothalamus.The role of the Rx homeobox gene in retinal progenitor proliferation and cell fate specification.
P2860
RAX and anophthalmia in humans: evidence of brain anomalies.
description
2012 nî lūn-bûn
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2012年の論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年论文
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name
RAX and anophthalmia in humans: evidence of brain anomalies.
@ast
RAX and anophthalmia in humans: evidence of brain anomalies.
@en
type
label
RAX and anophthalmia in humans: evidence of brain anomalies.
@ast
RAX and anophthalmia in humans: evidence of brain anomalies.
@en
prefLabel
RAX and anophthalmia in humans: evidence of brain anomalies.
@ast
RAX and anophthalmia in humans: evidence of brain anomalies.
@en
P2093
P2860
P1433
P1476
RAX and anophthalmia in humans: evidence of brain anomalies.
@en
P2093
Daniel F Schorderet
Hana Abouzeid
Iman Marzouk
Mohamed A Youssef
Nader Bayoumi
Nihal ElShakankiri
Philippe Hauser
P2860
P304
P577
2012-06-02T00:00:00Z