Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
about
Impact of FHIT loss on the translation of cancer-associated mRNAs.Neurodevelopmental disorders: Miniaturized protein offers treatment hopes for Rett syndrome.Rett syndrome: a neurological disorder with metabolic components.Rett syndrome from bench to bedside: recent advances.Autism spectrum disorder: prospects for treatment using gene therapy.A mutation-led search for novel functional domains in MeCP2.The Axon-Myelin Unit in Development and Degenerative DiseaseAffinity for DNA Contributes to NLS Independent Nuclear Localization of MeCP2
P2860
Q47105879-2E5F3009-AEC6-4A67-B7DE-975748F1920FQ47597770-A2C9CF40-48B7-405A-A01A-95CC28875ABFQ50422613-88EB8BD4-6586-4D35-BC7A-E4E81DE5AF36Q55312256-39CA49A4-F098-4590-886E-FDA94AC41B0DQ55339450-CECBB5F7-CFB1-48F0-9E8B-5C01A1F825D5Q55499199-F24B9402-78EC-41E3-A9EC-716074D8DEE5Q56000910-022ACEDA-FDE2-4104-B039-B87CD113E89AQ58697752-E7031D33-240A-4BC7-9C0D-3E2CCB7A1DEE
P2860
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
description
2017 nî lūn-bûn
@nan
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
2017年论文
@zh
2017年论文
@zh-cn
name
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
@en
type
label
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
@en
prefLabel
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.
@en
P2093
P2860
P50
P356
P1433
P1476
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects
@en
P2093
Dina De Sousa
Martha V Koerner
Rebekah Tillotson
Stuart R Cobb
P2860
P2888
P304
P356
10.1038/NATURE24058
P407
P577
2017-10-11T00:00:00Z
P6179
1092152723