Congenital diseases and semaphorin signaling: overview to date of the evidence linking them.

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An extracellular biochemical screen reveals that FLRTs and Unc5s mediate neuronal subtype recognition in the retina Contribution of semaphorins to the formation of the peripheral nervous system in higher vertebrates.View Point: Semaphorin-3E: An Emerging Modulator of Natural Killer Cell Functions?

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Congenital diseases and semaphorin signaling: overview to date of the evidence linking them.

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2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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Congenital diseases and semaph ...... of the evidence linking them.

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Congenital diseases and semaph ...... of the evidence linking them.

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Congenital diseases and semaph ...... of the evidence linking them.

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Congenital diseases and semaph ...... of the evidence linking them.

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Masahiko Taniguchi

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Tomoyuki Masuda

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P2860

Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes

Cone rod dystrophies

Plexins are a large family of receptors for transmembrane, secreted, and GPI-anchored semaphorins in vertebrates

Plexin-B3 is a functional receptor for semaphorin 5A.

Semaphorin-4A, an activator for T-cell-mediated immunity, suppresses angiogenesis via Plexin-D1

Plexin-a4 mediates axon-repulsive activities of both secreted and transmembrane semaphorins and plays roles in nerve fiber guidance

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

GATA6 mutations cause human cardiac outflow tract defects by disrupting semaphorin-plexin signaling

GATA-6 regulates semaphorin 3C and is required in cardiac neural crest for cardiovascular morphogenesis.

Dual roles of Sema6D in cardiac morphogenesis through region-specific association of its receptor, Plexin-A1, with off-track and vascular endothelial growth factor receptor type 2

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26-30

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scholarly article

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10.1111/CGA.12095

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2015-02-01T00:00:00Z

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25385160

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birth defect

Congenital diseases and semaphorin signaling: overview to date of the evidence linking them.

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P2860

P2860

Congenital diseases and semaphorin signaling: overview to date of the evidence linking them.

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P1433

P1476

P2093

P2860

P304

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P356

P433

P478

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P921