Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
about
Rai1 frees mice from the repression of active wake behaviors by light.Rai1 Haploinsufficiency Is Associated with Social Abnormalities in Mice.The interrelationship of metabolic syndrome and neurodegenerative diseases with focus on brain-derived neurotrophic factor (BDNF): Kill two birds with one stone.RAI1 gene mutations: mechanisms of Smith-Magenis syndrome.Reversed gender ratio of autism spectrum disorder in Smith-Magenis syndrome.A New Patient with Potocki-Lupski Syndrome: A Literature Review.A Rare De Novo RAI1 Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation.Early adolescent Rai1 reactivation reverses transcriptional and social interaction deficits in a mouse model of Smith-Magenis syndrome
P2860
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P2860
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
@en
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
@nl
type
label
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
@en
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
@nl
prefLabel
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
@en
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
@nl
P2093
P2860
P50
P1433
P1476
Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.
@en
P2093
Alex W Wilkinson
Casey J Guenthner
Howard Y Chang
Lindsay A Schwarz
Mehrdad Shamloo
Tiffany Nguyen
P2860
P304
P356
10.1016/J.NEURON.2016.09.019
P407
P577
2016-09-22T00:00:00Z