Page last updated: 2024-08-17

cycloheximide and Limb-Girdle Muscular Dystrophies

cycloheximide has been researched along with Limb-Girdle Muscular Dystrophies in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baas, F; Bashir, R; Bolduc, V; Boycott, KM; Brais, B; de Visser, M; Inoue, H; Itakura, M; Kamata, N; Kroon, J; Linssen, WH; Mahjneh, I; Marlow, G; Mizuta, K; Parent, L; Richard, I; Robitaille, Y; Saleki, K	1

Other Studies

1 other study(ies) available for cycloheximide and Limb-Girdle Muscular Dystrophies

Article	Year
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies. American journal of human genetics, 2010, Feb-12, Volume: 86, Issue:2 Topics: Adult; Aged; Anoctamins; Base Sequence; Canada; Chloride Channels; Codon, Nonsense; Cycloheximide; DNA Mutational Analysis; Dysferlin; Family; Female; Genes, Recessive; Humans; Male; Membrane Proteins; Middle Aged; Molecular Sequence Data; Muscle Proteins; Muscles; Muscular Dystrophies, Limb-Girdle; Mutation; Pedigree	2010

Article

Year

Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies.

American journal of human genetics, 2010, Feb-12, Volume: 86, Issue:2

Topics: Adult; Aged; Anoctamins; Base Sequence; Canada; Chloride Channels; Codon, Nonsense; Cycloheximide; DNA Mutational Analysis; Dysferlin; Family; Female; Genes, Recessive; Humans; Male; Membrane Proteins; Middle Aged; Molecular Sequence Data; Muscle Proteins; Muscles; Muscular Dystrophies, Limb-Girdle; Mutation; Pedigree

2010