Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle Laminopathies.

Autor: Nicolas HA; Department of Biology, Faculty of Science, University of Ottawa, Ottawa, ON K1N 6N5, Canada., Bertrand AT; Sorbonne Université, Inserm, Center of Research in Myology, Institute of Myology, F-75013 Paris, France., Labib S; Interdisciplinary School of Health Sciences, Faculty of Health Sciences, University of Ottawa, Ottawa, ON K1N 6N5, Canada., Mohamed-Uvaize M; Interdisciplinary School of Health Sciences, Faculty of Health Sciences, University of Ottawa, Ottawa, ON K1N 6N5, Canada., Bolongo PM; Interdisciplinary School of Health Sciences, Faculty of Health Sciences, University of Ottawa, Ottawa, ON K1N 6N5, Canada., Wu WY; Department of Biology, Faculty of Science, University of Ottawa, Ottawa, ON K1N 6N5, Canada., Bilińska ZT; Unit for Screening Studies in Inherited Cardiovascular Diseases, National Institute of Cardiology, 04-628 Warsaw, Poland., Bonne G; Sorbonne Université, Inserm, Center of Research in Myology, Institute of Myology, F-75013 Paris, France., Akimenko MA; Department of Biology, Faculty of Science, University of Ottawa, Ottawa, ON K1N 6N5, Canada., Tesson F; Interdisciplinary School of Health Sciences, Faculty of Health Sciences, University of Ottawa, Ottawa, ON K1N 6N5, Canada.

Publikováno v: Cells [Cells] 2020 Oct 31; Vol. 9 (11). Date of Electronic Publication: 2020 Oct 31.

Caenorhabditis elegans models for striated muscle disorders caused by missense variants of human LMNA.

Autor: Gregory, Ellen F.¹ (AUTHOR), Kalra, Shilpi¹ (AUTHOR), Brock, Trisha² (AUTHOR), Bonne, Gisèle³ (AUTHOR), Luxton, G. W. Gant¹ (AUTHOR), Hopkins, Christopher² (AUTHOR), Starr, Daniel A.¹ (AUTHOR) dastarr@ucdavis.edu

Publikováno v: PLoS Genetics. 8/25/2023, Vol. 19 Issue 8, p1-23. 23p.

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption.

Autor: Gupta P; Faculty of Health Sciences, University of Ottawa, Ottawa, ON, K1H 8M5, Canada., Bilinska ZT, Sylvius N, Boudreau E, Veinot JP, Labib S, Bolongo PM, Hamza A, Jackson T, Ploski R, Walski M, Grzybowski J, Walczak E, Religa G, Fidzianska A, Tesson F

Publikováno v: Basic research in cardiology [Basic Res Cardiol] 2010 May; Vol. 105 (3), pp. 365-77. Date of Electronic Publication: 2010 Feb 03.

Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report.

Autor: PENG FAN¹, DI ZHANG², KUN-QI YANG¹, TAO TIAN¹, FANG LUO¹, YA-XIN LIU², LIN-PING WANG¹ wanglping@139.com, XIAN-LIANG ZHOU¹

Publikováno v: Molecular Medicine Reports. Jun2020, Vol. 21 Issue 6, p2459-2465. 7p.

Genetic mutation of familial dilated cardiomyopathy based on next-generation semiconductor sequencing.

Autor: Lin, Xin-Fu^1,2, Luo, Jie-Wei^1,3 docluo0421@aliyun.com, Liu, Gui³, Zhu, Yao-Bin⁴, Jin, Zhao¹, Lin, Xing^1,5

Publikováno v: Molecular Medicine Reports. Nov2018, Vol. 18 Issue 5, p4271-4280. 10p.