Results 171 to 178 of about 1,999 (178)

A Nonsense ALMS1 Mutation Underlies Alström Syndrome in an Extended Mennonite Kindred Settled in North Mexico

Genetic Testing and Molecular Biomarkers, 2017
Marisa Cruz-Aguilar, CARLOS Galaviz-Hernández, Martha Sosa-Macias   +2 more
exaly  

A truncating mutation of Alms1 reduces the number of hypothalamic neuronal cilia in obese mice

Developmental Neurobiology, 2013
Claire Z Larter, Michel R Leroux
exaly  

Five novel ALMS1 gene mutations in six patients with Alström syndrome

Journal of Pediatric Endocrinology and Metabolism, 2018
Suna Kilinc, Didem Yücel-Yılmaz, Süheylâ Apaydin   +2 more
exaly  

Ophthalmic features of cone‐rod dystrophy caused by pathogenic variants in the ALMS1 gene

Acta Ophthalmologica, 2018
Fadi Nasser, Nicole Weißschuh, Pietro Maffei   +2 more
exaly  

Knockdown of the Alström syndrome-associated gene Alms1 in 3T3-L1 preadipocytes impairs adipogenesis but has no effect on cell-autonomous insulin action

International Journal of Obesity, 2010
Isabel Huang-Doran, Robert K Semple, Semple R K   +2 more
exaly  

Alström syndrome: intrafamilial phenotypic variability in sibs with a novel nonsense mutation of the ALMS1 gene

Clinical Genetics, 2004
TITOMANLIO, LUIGI, DE BRASI, DANIELE, BUONINCONTI A, SPERANDEO MP, PEPE A, ANDRIA, GENEROSO, SEBASTIO, GIANFRANCO   +6 more
openaire   +3 more sources

Identification of a novel ALMS1 mutation in a Chinese family with Alström syndrome

Eye, 2009
exaly  

ALMS1-IT1: A Key Player in the Novel Disulfidptosis-Related LncRNA Prognostic Signature for Head and Neck Squamous Cell Carcinoma

Biomolecules
Xin-Yi Sun, Min Fu, Xi-Yuan Ge
exaly