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5. Phenotypic behavior of caveolin-3 mutations that cause autosomal dominant limb girdle muscular dystrophy (LGMD-1C). Retention of LGMD-1C caveolin-3 mutants within the golgi complex. Galbiati F; Volonte D; Minetti C; Chu JB; Lisanti MP J Biol Chem; 1999 Sep; 274(36):25632-41. PubMed ID: 10464299 [TBL] [Abstract][Full Text] [Related]
6. Caveolin and NOS in the Development of Muscular Dystrophy. Nakashima M; Suga N; Yoshikawa S; Matsuda S Int J Mol Sci; 2024 Aug; 25(16):. PubMed ID: 39201459 [TBL] [Abstract][Full Text] [Related]
7. Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-like muscular dystrophy phenotype. Galbiati F; Volonte D; Chu JB; Li M; Fine SW; Fu M; Bermudez J; Pedemonte M; Weidenheim KM; Pestell RG; Minetti C; Lisanti MP Proc Natl Acad Sci U S A; 2000 Aug; 97(17):9689-94. PubMed ID: 10931944 [TBL] [Abstract][Full Text] [Related]
8. Caveolin-3 null mice show a loss of caveolae, changes in the microdomain distribution of the dystrophin-glycoprotein complex, and t-tubule abnormalities. Galbiati F; Engelman JA; Volonte D; Zhang XL; Minetti C; Li M; Hou H; Kneitz B; Edelmann W; Lisanti MP J Biol Chem; 2001 Jun; 276(24):21425-33. PubMed ID: 11259414 [TBL] [Abstract][Full Text] [Related]
9. Impairment of caveolae formation and T-system disorganization in human muscular dystrophy with caveolin-3 deficiency. Minetti C; Bado M; Broda P; Sotgia F; Bruno C; Galbiati F; Volonte D; Lucania G; Pavan A; Bonilla E; Lisanti MP; Cordone G Am J Pathol; 2002 Jan; 160(1):265-70. PubMed ID: 11786420 [TBL] [Abstract][Full Text] [Related]
10. Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation. Merrick D; Stadler LK; Larner D; Smith J Dis Model Mech; 2009; 2(7-8):374-88. PubMed ID: 19535499 [TBL] [Abstract][Full Text] [Related]
11. Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy. Herrmann R; Straub V; Blank M; Kutzick C; Franke N; Jacob EN; Lenard HG; Kröger S; Voit T Hum Mol Genet; 2000 Sep; 9(15):2335-40. PubMed ID: 11001938 [TBL] [Abstract][Full Text] [Related]
12. Limb-girdle muscular dystrophy (LGMD-1C) mutants of caveolin-3 undergo ubiquitination and proteasomal degradation. Treatment with proteasomal inhibitors blocks the dominant negative effect of LGMD-1C mutanta and rescues wild-type caveolin-3. Galbiati F; Volonte D; Minetti C; Bregman DB; Lisanti MP J Biol Chem; 2000 Dec; 275(48):37702-11. PubMed ID: 10973975 [TBL] [Abstract][Full Text] [Related]
14. Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy. Repetto S; Bado M; Broda P; Lucania G; Masetti E; Sotgia F; Carbone I; Pavan A; Bonilla E; Cordone G; Lisanti MP; Minetti C Biochem Biophys Res Commun; 1999 Aug; 261(3):547-50. PubMed ID: 10441463 [TBL] [Abstract][Full Text] [Related]
15. Angiogenic impairment of the vascular endothelium: a novel mechanism and potential therapeutic target in muscular dystrophy. Palladino M; Gatto I; Neri V; Straino S; Smith RC; Silver M; Gaetani E; Marcantoni M; Giarretta I; Stigliano E; Capogrossi M; Hlatky L; Landolfi R; Pola R Arterioscler Thromb Vasc Biol; 2013 Dec; 33(12):2867-76. PubMed ID: 24072696 [TBL] [Abstract][Full Text] [Related]
16. Loss of caveolin-3 induced by the dystrophy-associated P104L mutation impairs L-type calcium channel function in mouse skeletal muscle cells. Couchoux H; Allard B; Legrand C; Jacquemond V; Berthier C J Physiol; 2007 May; 580(Pt.3):745-54. PubMed ID: 17317753 [TBL] [Abstract][Full Text] [Related]
17. Zebrafish as a model for caveolin-associated muscle disease; caveolin-3 is required for myofibril organization and muscle cell patterning. Nixon SJ; Wegner J; Ferguson C; Méry PF; Hancock JF; Currie PD; Key B; Westerfield M; Parton RG Hum Mol Genet; 2005 Jul; 14(13):1727-43. PubMed ID: 15888488 [TBL] [Abstract][Full Text] [Related]
18. The biology of caveolae: lessons from caveolin knockout mice and implications for human disease. Hnasko R; Lisanti MP Mol Interv; 2003 Dec; 3(8):445-64. PubMed ID: 14993453 [TBL] [Abstract][Full Text] [Related]
19. The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle. Matsuda C; Hayashi YK; Ogawa M; Aoki M; Murayama K; Nishino I; Nonaka I; Arahata K; Brown RH Hum Mol Genet; 2001 Aug; 10(17):1761-6. PubMed ID: 11532985 [TBL] [Abstract][Full Text] [Related]
20. Filopodia powered by class x myosin promote fusion of mammalian myoblasts. Hammers DW; Hart CC; Matheny MK; Heimsath EG; Lee YI; Hammer JA; Cheney RE; Sweeney HL Elife; 2021 Sep; 10():. PubMed ID: 34519272 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]