Page last updated: 2024-08-18

xanthenes and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

xanthenes has been researched along with Autosomal Recessive Emery-Dreifuss Muscular Dystrophy in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Egashira, T; Fukuda, K; Hashimoto, H; Hayashi, K; Hayashiji, N; Ito, S; Kashimura, S; Kodaira, M; Kunitomi, A; Kusumoto, D; Lachmann, M; Motoda, C; Nagai, T; Nakanishi, C; Sakata, K; Seki, T; Shimojima, M; Takei, M; Tohyama, S; Yamagishi, M; Yozu, G; Yuasa, S1
Buendia, B; Dabauvalle, MC; Kandert, S; Müller, CR; Wehnert, M1

Other Studies

2 other study(ies) available for xanthenes and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

ArticleYear
Emerin plays a crucial role in nuclear invagination and in the nuclear calcium transient.
    Scientific reports, 2017, 03-14, Volume: 7

    Topics: Active Transport, Cell Nucleus; Angiotensin II; Aniline Compounds; Animals; Atrial Remodeling; Calcium; Cardiomegaly; Cytoplasm; Disease Models, Animal; Endothelin-1; Fluorescent Dyes; Gene Expression Regulation; Heterocyclic Compounds, 3-Ring; Humans; Membrane Proteins; Muscular Dystrophy, Emery-Dreifuss; Myocardium; Myocytes, Cardiac; Nuclear Envelope; Nuclear Proteins; Phenylephrine; Primary Cell Culture; Rats; Rats, Sprague-Dawley; RNA, Small Interfering; Ventricular Remodeling; Xanthenes

2017
Impaired nuclear functions lead to increased senescence and inefficient differentiation in human myoblasts with a dominant p.R545C mutation in the LMNA gene.
    European journal of cell biology, 2009, Volume: 88, Issue:10

    Topics: Aging; Amino Acid Substitution; Antibodies; Bisbenzimidazole; Carbocyanines; Case-Control Studies; Cell Culture Techniques; Cell Differentiation; Cell Nucleus; Cells, Cultured; Cysteine; Female; Fluorescein-5-isothiocyanate; Fluorescent Dyes; Humans; Lamin Type A; Male; Muscular Dystrophy, Emery-Dreifuss; Mutation, Missense; Myoblasts; Point Mutation; Xanthenes

2009