Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis
about
Wolframin expression induces novel ion channel activity in endoplasmic reticulum membranes and increases intracellular calciumWolfram syndrome 1 gene negatively regulates ER stress signaling in rodent and human cellsWolfram syndrome: new mutations, different phenotypeImpact of type 2 diabetes susceptibility variants on quantitative glycemic traits reveals mechanistic heterogeneity.Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss.Current knowledge of Japanese type 1 diabetic syndrome.Genetic epidemiology of type 1 diabetes.Monogenic Diabetes: What It Teaches Us on the Common Forms of Type 1 and Type 2 Diabetes.Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation.Endoplasmic reticulum stress and eIF2α phosphorylation: The Achilles heel of pancreatic β cells.WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims.Evidence for linkage on chromosome 4p16.1 in Type 1 diabetes Danish families and complete mutation scanning of the WFS1 (Wolframin) gene.WFS1 mutations in Spanish patients with diabetes mellitus and deafness
P2860
Q24296961-95008027-8472-4A42-9548-54EA603F6BB5Q24299603-DACDAB52-EB17-4D7F-A46B-C03A8D98022CQ28478694-B8A4FDC3-3770-45A7-81A4-9358D5573CD7Q33646698-9E5F9686-D529-4612-B818-C258164D3A26Q34527976-D1064EE0-0353-4273-B97C-2249032D6786Q34979242-29F1ECB8-0BE2-4CF6-9046-4B004F98A564Q35600184-AA18668A-9399-4613-ADE5-FFC558614CC1Q36960085-26D972E1-64D7-47DF-BE0F-63C00126315DQ37251162-3CFC75B5-8B3F-41DE-9D1E-3DA2D3000FA5Q41689677-B8FF5269-389C-4214-9D09-F6A17CFED1E9Q44793653-17A914A5-DD68-4827-B65C-AC7809F3185AQ47982108-9E6E9B95-BADC-4BD8-B4AB-A52E7C0AFDE0Q55670953-10F25F14-5725-4BFD-8A29-9E867EF583AB
P2860
Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis
description
2000 nî lūn-bûn
@nan
2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Missense variations of the gen ...... a nonautoimmune genetic basis
@ast
Missense variations of the gen ...... a nonautoimmune genetic basis
@en
Missense variations of the gen ...... a nonautoimmune genetic basis
@nl
type
label
Missense variations of the gen ...... a nonautoimmune genetic basis
@ast
Missense variations of the gen ...... a nonautoimmune genetic basis
@en
Missense variations of the gen ...... a nonautoimmune genetic basis
@nl
prefLabel
Missense variations of the gen ...... a nonautoimmune genetic basis
@ast
Missense variations of the gen ...... a nonautoimmune genetic basis
@en
Missense variations of the gen ...... a nonautoimmune genetic basis
@nl
P2093
P356
P1476
Missense variations of the gen ...... a nonautoimmune genetic basis
@en
P2093
Kanazawa Y
Katayama S
Kurihara S
P304
P356
10.1006/BBRC.2000.2169
P407
P50
P577
2000-02-01T00:00:00Z