Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntington's disease.
about
Enhanced neuronal glucose transporter expression reveals metabolic choice in a HD Drosophila modelDetermining multiallelic complex copy number and sequence variation from high coverage exome sequencing dataAvian and Mammalian Facilitative Glucose Transporters.Mechanisms and consequences of aneuploidy and chromosome instability in the aging brainCopy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.Beyond the redox imbalance: Oxidative stress contributes to an impaired GLUT3 modulation in Huntington's diseaseMetabolic Dysfunction in Parkinson's Disease: Bioenergetics, Redox Homeostasis and Central Carbon Metabolism.Brain metabolism in health, aging, and neurodegeneration.Towards an Understanding of Energy Impairment in Huntington's Disease Brain.SLC2A3 single-nucleotide polymorphism and duplication influence cognitive processing and population-specific risk for attention-deficit/hyperactivity disorder.Autosomal and X chromosome structural variants are associated with congenital heart defects in Turner syndrome: The NHLBI GenTAC registry.
P2860
Q28389710-66696291-2DB4-4AA6-9C94-8117F14F32E0Q31015139-81F3DD02-1102-4711-B4D5-1785FFE2F2DBQ33844784-B94C01BF-ECC4-48E2-BD4B-23D615DCB8B6Q33850635-82D67AE8-1623-4888-9739-7C873E3E571BQ36060851-6CEF77D9-152B-4A6B-B1EB-2A8697158638Q36824396-3ADDCAE9-CF93-4246-BE3C-B0AFAFE0BAD2Q39199926-C8240ECA-7610-4E52-8854-5350937B26F3Q39259780-31DB0C2D-D1B5-4D39-8038-46B2318FFBE0Q47442924-73910747-0DBB-4D7F-ACD4-B360C8EB2512Q47794013-6C759E53-A1D8-4AAF-BB09-4A096D172EB0Q52850139-2FDA1425-1499-4909-BCC2-666FDB43EF7F
P2860
Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntington's disease.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հունվարին հրատարակված գիտական հոդված
@hy
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
name
Copy-number variation of the n ...... onset in Huntington's disease.
@ast
Copy-number variation of the n ...... onset in Huntington's disease.
@en
type
label
Copy-number variation of the n ...... onset in Huntington's disease.
@ast
Copy-number variation of the n ...... onset in Huntington's disease.
@en
prefLabel
Copy-number variation of the n ...... onset in Huntington's disease.
@ast
Copy-number variation of the n ...... onset in Huntington's disease.
@en
P2093
P2860
P50
P356
P1476
Copy-number variation of the n ...... onset in Huntington's disease.
@en
P2093
Angelica Vittori
Flaviano Giorgini
Michael Orth
REGISTRY investigators of the European Huntington's Disease Network
Raymund A C Roos
P2860
P304
P356
10.1093/HMG/DDU022
P577
2014-01-22T00:00:00Z