about
Dcc Mediates Functional Assembly of Peripheral Auditory CircuitsActin dynamics in growth cone motility and navigationThe Netrin-1 receptor DCC is a regulator of maladaptive responses to chronic morphine administrationNetrin-1 stimulates developing GnRH neurons to extend neurites to the median eminence in a calcium- dependent mannerAspirin-induced histone acetylation in endothelial cells enhances synthesis of the secreted isoform of netrin-1 thus inhibiting monocyte vascular infiltration.Hsc70 chaperone activity underlies Trio GEF function in axon growth and guidance induced by netrin-1.Human disorders of axon guidance.Genome-wide pathway analysis of memory impairment in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort implicates gene candidates, canonical pathways, and networks.Evolution of the functionally conserved DCC gene in birdsThe tangled web of non-canonical Wnt signalling in neural migration.Biallelic mutations in human DCC cause developmental split-brain syndrome.Pyramidal tract abnormalities in the human fetus and infant with trisomy 18 syndrome.In vivo Functional Analysis of Drosophila Robo1 Fibronectin Type III Repeats.Behavioral Consequences of a Bifacial Map in the Mouse Somatosensory Cortex.Midline axon guidance in the Drosophila embryonic central nervous system.Undecussated superior cerebellar peduncles and absence of the dorsal transverse pontine fibers: a new axonal guidance disorder?The Midline Axon Crossing Decision Is Regulated through an Activity-Dependent Mechanism by the NMDA Receptor.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Midline axon guidance and human genetic disorders.
@ast
Midline axon guidance and human genetic disorders.
@en
Midline axon guidance and human genetic disorders.
@nl
type
label
Midline axon guidance and human genetic disorders.
@ast
Midline axon guidance and human genetic disorders.
@en
Midline axon guidance and human genetic disorders.
@nl
prefLabel
Midline axon guidance and human genetic disorders.
@ast
Midline axon guidance and human genetic disorders.
@en
Midline axon guidance and human genetic disorders.
@nl
P2860
P1433
P1476
Midline axon guidance and human genetic disorders.
@en
P2093
P2860
P304
P356
10.1111/J.1399-0004.2011.01735.X
P577
2011-07-25T00:00:00Z