Functional annotation of genes overlapping copy number variants in autistic patients: focus on axon pathfinding.
about
Novel autism subtype-dependent genetic variants are revealed by quantitative trait and subphenotype association analyses of published GWAS dataThe neuroanatomy of autism - a developmental perspectiveLargely typical patterns of resting-state functional connectivity in high-functioning adults with autismDIA1R is an X-linked gene related to Deleted In Autism-1.Biochip∕laser cell deposition system to assess polarized axonal growth from single neurons and neuron∕glia pairs in microchannels with novel asymmetrical geometriesBrain transcriptional and epigenetic associations with autism.Dovetailing biology and chemistry: integrating the Gene Ontology with the ChEBI chemical ontology.Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons.Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study.Evidence for dysregulation of axonal growth and guidance in the etiology of ASD.Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavin.Stem cells as a good tool to investigate dysregulated biological systems in autism spectrum disorders.Neurobiology meets genomic science: the promise of human-induced pluripotent stem cells.
P2860
Q21135474-B093593D-A109-4FB5-82D0-DCC5EA9E323BQ28973599-535226D1-8902-42A7-87FA-718CA99BD974Q33735131-3769D003-2E01-4216-A9A4-BF8EB716DB23Q33802577-9FCA8799-B5BA-4432-B4B0-5B860640F608Q33882554-A787BC46-CFEB-48F9-A7CF-8AFE1CF64DE9Q34416063-686AC2EE-4C29-4E60-94FE-7B6ADEB458EDQ34878068-98E08D20-1961-422B-A4A3-8B99D109A784Q35593898-F0E68EE9-333F-4CD1-9D3C-1C1FAF871C74Q36738328-8A560020-883C-4700-AD35-95166B1D8EC4Q37246408-17A4A56B-62A4-4CC8-8524-16902EA170A6Q37739698-72364A62-630F-4797-8F1F-F72AE233899DQ38314579-35E2829D-258D-41D9-9AE8-0A71DC53AA06Q42385406-F0305B7D-31AD-4723-B355-5E20145995AC
P2860
Functional annotation of genes overlapping copy number variants in autistic patients: focus on axon pathfinding.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Functional annotation of genes ...... ts: focus on axon pathfinding.
@en
type
label
Functional annotation of genes ...... ts: focus on axon pathfinding.
@en
prefLabel
Functional annotation of genes ...... ts: focus on axon pathfinding.
@en
P2093
P2860
P1433
P1476
Functional annotation of genes ...... ts: focus on axon pathfinding.
@en
P2093
Francesco Acquadro
Ignazio Calò
Silvia Sbacchi
P2860
P304
P356
10.2174/138920210790886880
P577
2010-04-01T00:00:00Z