Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function.
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JIP3 Activates Kinesin-1 Motility to Promote Axon ElongationMGFM: a novel tool for detection of tissue and cell specific marker genes from microarray gene expression dataSIRT1-FOXO3a regulate cocaine actions in the nucleus accumbens.Identification of genes that promote or inhibit olfactory memory formation in Drosophila.De Novo Mutations in CHAMP1 Cause Intellectual Disability with Severe Speech Impairment.Molecular subtyping and improved treatment of neurodevelopmental disease.An emerging role for mitochondrial dynamics in schizophrenia.Potential Role of Microtubule Stabilizing Agents in Neurodevelopmental Disorders.Recurrent KIF2A mutations are responsible for classic lissencephaly.KIF1A mediates axonal transport of BACE1 and identification of independently moving cargoes in living SCG neurons.Genetics of intellectual disability in consanguineous families.A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency.Kinesin KIF4A is associated with chemotherapeutic drug resistance by regulating intracellular trafficking of lung resistance-related protein.Role of maternal Xenopus syntabulin in germ plasm aggregation and primordial germ cell specification.Challenges and opportunities in the investigation of unexplained intellectual disability using family-based whole-exome sequencing.Network analysis of UBE3A/E6AP-associated proteins provides connections to several distinct cellular processes.Lissencephaly: Expanded imaging and clinical classification.Mutations of KIF5C cause a neurodevelopmental disorder of infantile-onset epilepsy, absent language, and distinctive malformations of cortical development.Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly.ATG5 overexpression is neuroprotective and attenuates cytoskeletal and vesicle-trafficking alterations in axotomized motoneurons.The Role of the Microtubule Cytoskeleton in Neurodevelopmental Disorders.Recurrent KIF5C mutation leading to frontal pachygyria without microcephalyComprehensive genotype-phenotype correlation in lissencephaly
P2860
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P2860
Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Involvement of the kinesin fam ...... ability and synaptic function.
@en
type
label
Involvement of the kinesin fam ...... ability and synaptic function.
@en
prefLabel
Involvement of the kinesin fam ...... ability and synaptic function.
@en
P2093
P2860
P50
P1476
Involvement of the kinesin fam ...... sability and synaptic function
@en
P2093
Arjan P M de Brouwer
Marjolein H Willemsen
Melanie Bienek
Tjitske Kleefstra
Willemijn M Wissink-Lindhout
P2860
P304
P356
10.1136/JMEDGENET-2013-102182
P407
P577
2014-05-08T00:00:00Z