These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
247 related articles for article (PubMed ID: 19015158)
1. Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue. Hicks D; Lampe AK; Laval SH; Allamand V; Jimenez-Mallebrera C; Walter MC; Muntoni F; Quijano-Roy S; Richard P; Straub V; Lochmüller H; Bushby KM Brain; 2009 Jan; 132(Pt 1):147-55. PubMed ID: 19015158 [TBL] [Abstract][Full Text] [Related]
5. Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy. Baker NL; Mörgelin M; Peat R; Goemans N; North KN; Bateman JF; Lamandé SR Hum Mol Genet; 2005 Jan; 14(2):279-93. PubMed ID: 15563506 [TBL] [Abstract][Full Text] [Related]
6. Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 loci. Demir E; Ferreiro A; Sabatelli P; Allamand V; Makri S; Echenne B; Maraldi M; Merlini L; Topaloglu H; Guicheney P Neuropediatrics; 2004 Apr; 35(2):103-12. PubMed ID: 15127309 [TBL] [Abstract][Full Text] [Related]
7. NIM811, a cyclophilin inhibitor without immunosuppressive activity, is beneficial in collagen VI congenital muscular dystrophy models. Zulian A; Rizzo E; Schiavone M; Palma E; Tagliavini F; Blaauw B; Merlini L; Maraldi NM; Sabatelli P; Braghetta P; Bonaldo P; Argenton F; Bernardi P Hum Mol Genet; 2014 Oct; 23(20):5353-63. PubMed ID: 24852368 [TBL] [Abstract][Full Text] [Related]
8. Dysfunction of mitochondria and sarcoplasmic reticulum in the pathogenesis of collagen VI muscular dystrophies. Bernardi P; Bonaldo P Ann N Y Acad Sci; 2008 Dec; 1147():303-11. PubMed ID: 19076452 [TBL] [Abstract][Full Text] [Related]
9. Mitochondrial dysfunction and defective autophagy in the pathogenesis of collagen VI muscular dystrophies. Bernardi P; Bonaldo P Cold Spring Harb Perspect Biol; 2013 May; 5(5):a011387. PubMed ID: 23580791 [TBL] [Abstract][Full Text] [Related]
10. Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance. Lampe AK; Zou Y; Sudano D; O'Brien KK; Hicks D; Laval SH; Charlton R; Jimenez-Mallebrera C; Zhang RZ; Finkel RS; Tennekoon G; Schreiber G; van der Knaap MS; Marks H; Straub V; Flanigan KM; Chu ML; Muntoni F; Bushby KM; Bönnemann CG Hum Mutat; 2008 Jun; 29(6):809-22. PubMed ID: 18366090 [TBL] [Abstract][Full Text] [Related]
11. Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies. Tagliavini F; Pellegrini C; Sardone F; Squarzoni S; Paulsson M; Wagener R; Gualandi F; Trabanelli C; Ferlini A; Merlini L; Santi S; Maraldi NM; Faldini C; Sabatelli P Biochim Biophys Acta; 2014 Sep; 1842(9):1604-12. PubMed ID: 24907562 [TBL] [Abstract][Full Text] [Related]
12. Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotype. Scacheri PC; Gillanders EM; Subramony SH; Vedanarayanan V; Crowe CA; Thakore N; Bingler M; Hoffman EP Neurology; 2002 Feb; 58(4):593-602. PubMed ID: 11865138 [TBL] [Abstract][Full Text] [Related]
13. Collagen type VI myopathies. Bushby KM; Collins J; Hicks D Adv Exp Med Biol; 2014; 802():185-99. PubMed ID: 24443028 [TBL] [Abstract][Full Text] [Related]
14. Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice. Palma E; Tiepolo T; Angelin A; Sabatelli P; Maraldi NM; Basso E; Forte MA; Bernardi P; Bonaldo P Hum Mol Genet; 2009 Jun; 18(11):2024-31. PubMed ID: 19293339 [TBL] [Abstract][Full Text] [Related]
15. Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis. Sabatelli P; Gualandi F; Gara SK; Grumati P; Zamparelli A; Martoni E; Pellegrini C; Merlini L; Ferlini A; Bonaldo P; Maraldi NM; Paulsson M; Squarzoni S; Wagener R Matrix Biol; 2012 Apr; 31(3):187-96. PubMed ID: 22226732 [TBL] [Abstract][Full Text] [Related]
16. Muscle interstitial fibroblasts are the main source of collagen VI synthesis in skeletal muscle: implications for congenital muscular dystrophy types Ullrich and Bethlem. Zou Y; Zhang RZ; Sabatelli P; Chu ML; Bönnemann CG J Neuropathol Exp Neurol; 2008 Feb; 67(2):144-54. PubMed ID: 18219255 [TBL] [Abstract][Full Text] [Related]
17. Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency. Irwin WA; Bergamin N; Sabatelli P; Reggiani C; Megighian A; Merlini L; Braghetta P; Columbaro M; Volpin D; Bressan GM; Bernardi P; Bonaldo P Nat Genet; 2003 Dec; 35(4):367-71. PubMed ID: 14625552 [TBL] [Abstract][Full Text] [Related]