Results 141 to 150 of about 2,671 (159)

Variation in ovine CAPN3 is not associated with meat tenderness

Animal Genetics, 2009
H, Zhou, C M, Frampton, J G H, Hickford
openaire   +2 more sources

Screening of the CAPN3 gene in patients with possible LGMD2A

Clinical Genetics, 2006
Martin, Krahn, Rafaelle, Bernard, Christophe, Pecheux, El Hadi, Hammouda, Bruno, Eymard, Adolfo, Lopez de Munain, Anna Maria, Cobo, Norma, Romero, Andoni, Urtizberea, France, Leturcq, Nicolas, Levy   +10 more
openaire   +2 more sources

Novel CAPN3 variant associated with an autosomal dominant calpainopathy

Neuropathology and Applied Neurobiology, 2020
Nicolas Levy, Svetlana Gorokhova, Cintas Pascal   +2 more
exaly  

CAPN3 c.1746‐20C>G variant is hypomorphic for LGMD R1 calpain 3‐related

Human Mutation, 2022
Baiba Lace, Sanna Puusepp, Lenka Fajkusova   +2 more
exaly  

Heterozygous CAPN3 missense variants causing autosomal‐dominant calpainopathy in seven unrelated families

Neuropathology and Applied Neurobiology, 2021
C Domínguez-González, Montse Olive, Fabiola Mavillard   +2 more
exaly  

Nucleolus-localized Def-CAPN3 protein degradation pathway and its role in cell cycle control and ribosome biogenesis

Journal of Genetics and Genomics, 2021
Jinrong Peng, Delai Huang, Shuyi Zhao
exaly  

Characterization of the eosinophilic myositis caused by CAPN3 mutations on a mouse model

Neuromuscular Disorders, 2017
Warnez-Soulie, J., Giannesini, B., Henri, S., Richard, I., Malissen, Bernard, Krahn, M., Bartoli, Marc   +6 more
openaire   +2 more sources

Bovine CAPN3 core promoter initiates expression of foreign genes in skeletal muscle cells by MyoD transcriptional regulation

International Journal of Biochemistry and Cell Biology, 2020
Luxing Ge, Xu Liu, Fusheng Quan
exaly  

Characterization of the Goose <i>CAPN3</i> Gene and its Expression Pattern in Muscle Tissues of Sichuan White Geese at Different Growth Stages

Journal of Poultry Science, 2018
Liang Li, Hengyong Xu, Hehe Liu
exaly  

P.187CAPN3 c.598_612delTTCTGGAGTGCTCTG: another CAPN3 dominant variant?

Neuromuscular Disorders, 2019
M. Mroczek, A. Töpf, J. Duff, R. Barresi, J. Hudson, E. England, K. Chao, D. MacArthur, V. Straub, null MYO-SEQ consortium   +9 more
openaire   +1 more source