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Characterization of ocular motor deficits in congenital facial weakness: Moebius and related syndromes.Variability of Ponto-cerebellar Fibers by Diffusion Tensor Imaging in Diverse Brain Malformations.Structural and functional brain rewiring clarifies preserved interhemispheric transfer in humans born without the corpus callosum.The structural connectome of the human brain in agenesis of the corpus callosumIn-lab three-dimensional printing: an inexpensive tool for experimentation and visualization for the field of organogenesis.Slit2 inactivates GSK3β to signal neurite outgrowth inhibition.A forward genetic screen in mice identifies mutants with abnormal cortical patterning.Transcriptomic analysis of pancreatic cancer cells in response to metformin and aspirin: an implication of synergy.Developmental Wiring of Specific Neurons Is Regulated by RET-1/Nogo-A in Caenorhabditis elegans.Insights into the biological functions of Dock family guanine nucleotide exchange factors.Cell adhesion and invasion mechanisms that guide developing axonsBiallelic mutations in human DCC cause developmental split-brain syndrome.Chondroitin sulfates and their binding molecules in the central nervous system.Analyzing kinesin motor domain translocation in cultured hippocampal neurons.Diabetic neuropathy and the sensory apparatus "meissner corpuscle and merkel cells".Mutant α2-chimaerin signals via bidirectional ephrin pathways in Duane retraction syndromeIdentifying splicing regulatory elements with de Bruijn graphs.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.The Absence of Sensory Axon Bifurcation Affects Nociception and Termination Fields of Afferents in the Spinal Cord.Alternating Hypotropia with Pseudoptosis: A New Phenotype of Congenital Cranial Dysinnervation Disorder.Molecular Analysis of Sensory Axon Branching Unraveled a cGMP-Dependent Signaling Cascade.Loss of Axon Bifurcation in Mesencephalic Trigeminal Neurons Impairs the Maximal Biting Force in Npr2-Deficient Mice.
P2860
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P2860
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Human disorders of axon guidance.
@ast
Human disorders of axon guidance.
@en
type
label
Human disorders of axon guidance.
@ast
Human disorders of axon guidance.
@en
prefLabel
Human disorders of axon guidance.
@ast
Human disorders of axon guidance.
@en
P2093
P2860
P1476
Human disorders of axon guidance.
@en
P2093
Adrianne L Kolpak
Alicia A Nugent
Elizabeth C Engle
P2860
P304
P356
10.1016/J.CONB.2012.02.006
P577
2012-03-05T00:00:00Z