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4. An alphaTropomyosin mutation alters dimer preference in nemaline myopathy. Corbett MA; Akkari PA; Domazetovska A; Cooper ST; North KN; Laing NG; Gunning PW; Hardeman EC Ann Neurol; 2005 Jan; 57(1):42-9. PubMed ID: 15562513 [TBL] [Abstract][Full Text] [Related]
5. Muscle weakness in a mouse model of nemaline myopathy can be reversed with exercise and reveals a novel myofiber repair mechanism. Joya JE; Kee AJ; Nair-Shalliker V; Ghoddusi M; Nguyen MA; Luther P; Hardeman EC Hum Mol Genet; 2004 Nov; 13(21):2633-45. PubMed ID: 15367485 [TBL] [Abstract][Full Text] [Related]
6. Disease severity and thin filament regulation in M9R TPM3 nemaline myopathy. Ilkovski B; Mokbel N; Lewis RA; Walker K; Nowak KJ; Domazetovska A; Laing NG; Fowler VM; North KN; Cooper ST J Neuropathol Exp Neurol; 2008 Sep; 67(9):867-77. PubMed ID: 18716557 [TBL] [Abstract][Full Text] [Related]
7. Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy. Nguyen MA; Joya JE; Kee AJ; Domazetovska A; Yang N; Hook JW; Lemckert FA; Kettle E; Valova VA; Robinson PJ; North KN; Gunning PW; Mitchell CA; Hardeman EC Brain; 2011 Dec; 134(Pt 12):3516-29. PubMed ID: 22067542 [TBL] [Abstract][Full Text] [Related]
9. Alterations at the cross-bridge level are associated with a paradoxical gain of muscle function in vivo in a mouse model of nemaline myopathy. Gineste C; Ottenheijm C; Le Fur Y; Banzet S; Pecchi E; Vilmen C; Cozzone PJ; Koulmann N; Hardeman EC; Bendahan D; Gondin J PLoS One; 2014; 9(9):e109066. PubMed ID: 25268244 [TBL] [Abstract][Full Text] [Related]
10. Rod distribution and muscle fiber type modification in the progression of nemaline myopathy. Gurgel-Giannetti J; Reed UC; Marie SK; Zanoteli E; Fireman MA; Oliveira AS; Werneck LC; Beggs AH; Zatz M; Vainzof M J Child Neurol; 2003 Mar; 18(3):235-40. PubMed ID: 12731651 [TBL] [Abstract][Full Text] [Related]
11. Combined cap disease and nemaline myopathy in the same patient caused by an autosomal dominant mutation in the TPM3 gene. Malfatti E; Schaeffer U; Chapon F; Yang Y; Eymard B; Xu R; Laporte J; Romero NB Neuromuscul Disord; 2013 Dec; 23(12):992-7. PubMed ID: 24095155 [TBL] [Abstract][Full Text] [Related]
13. A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy. Corbett MA; Robinson CS; Dunglison GF; Yang N; Joya JE; Stewart AW; Schnell C; Gunning PW; North KN; Hardeman EC Hum Mol Genet; 2001 Feb; 10(4):317-28. PubMed ID: 11157795 [TBL] [Abstract][Full Text] [Related]
14. Sexually dimorphic myofilament function in a mouse model of nemaline myopathy. Lindqvist J; Hardeman EC; Ochala J Arch Biochem Biophys; 2014 Dec; 564():37-42. PubMed ID: 25261348 [TBL] [Abstract][Full Text] [Related]
15. Severe neonatal nemaline myopathy with delayed maturation of muscle. Wada H; Nishio H; Kugo M; Waku S; Ikeda K; Takada S; Murakami R; Itoh H; Matsuo M; Nakamura H Brain Dev; 1996; 18(2):135-8. PubMed ID: 8733906 [TBL] [Abstract][Full Text] [Related]
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18. Expression and biological activity of Baculovirus generated wild-type human slow alpha tropomyosin and the Met9Arg mutant responsible for a dominant form of nemaline myopathy. Akkari PA; Song Y; Hitchcock-DeGregori S; Blechynden L; Laing N Biochem Biophys Res Commun; 2002 Aug; 296(2):300-4. PubMed ID: 12163017 [TBL] [Abstract][Full Text] [Related]
19. Triggering typical nemaline myopathy with compound heterozygous nebulin mutations reveals myofilament structural changes as pathomechanism. Lindqvist J; Ma W; Li F; Hernandez Y; Kolb J; Kiss B; Tonino P; van der Pijl R; Karimi E; Gong H; Strom J; Hourani Z; Smith JE; Ottenheijm C; Irving T; Granzier H Nat Commun; 2020 Jun; 11(1):2699. PubMed ID: 32483185 [TBL] [Abstract][Full Text] [Related]
20. Clinico-pathological and gene features of 15 nemaline myopathy patients from a single Chinese neuromuscular center. Haidong L; Yin L; Ping C; Xianzhao Z; Qi Q; Xiaoli M; Zheng L; Wenhao C; Yaguang Z; Qianqian Q Acta Neurol Belg; 2024 Feb; 124(1):91-99. PubMed ID: 37525074 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]