Results 171 to 180 of about 2,517,817 (182)

Mutational Analysis of the Wolfram Syndrome Gene (WFS1) in Greek and Dominican Patients

International Journal on Disability and Human Development, 2002
S. Bretschger, L. Deng, E. Caine, B. Boden-Albala, R. Sacco, R.L. Leibel, W.K. Chung   +6 more
openaire   +1 more source

Unmasking of a hemizygous WFS1 gene mutation by a chromosome 4p deletion of 8.3 Mb in a patient with Wolf–Hirschhorn syndrome

European Journal of Human Genetics, 2007
Peter M van Hasselt, Van Hasselt Peter M, Frits A Beemer   +2 more
exaly  

Hypothalamic gene expression profile indicates a reduction in G protein signaling in theWfs1mutant mice

Physiological Genomics, 2011
Eero Vasar, Sulev Koks, Leonard Schalkwyk   +2 more
exaly  

Wolfram syndrome and WFS1 gene

Clinical Genetics, 2011
exaly  

Expansion of the Clinical Ocular Spectrum of Wolfram Syndrome in a Family Carrying a NovelWFS1Gene Deletion

Ophthalmic Genetics, 2013
Juan Carlos Zenteno
exaly  

A novel heterozygous mutation of the WFS1 gene leading to constitutive endoplasmic reticulum stress is the cause of Wolfram syndrome

Pediatric Diabetes, 2017
Shuntaro Morikawa
exaly  

Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified

European Journal of Human Genetics, 2005
Toke Bek, Hans Eiberg, Timothy Barrett   +2 more
exaly  

Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in the WFS1 gene

Diabetic Medicine, 2008
exaly  

Rare variants in WFS1 gene in patients with young-onset diabetes

Четырнадцатая международная мультиконференция : Тез. докл.
openaire   +1 more source

Deletion of the Wolfram syndrome-related gene Wfs1 results in increased sensitivity to ethanol in female mice

Neuropharmacology, 2015
Eero Vasar, Hendrik Luuk, Tanel Visnapuu   +2 more
exaly