270 related articles for article (PubMed ID: 11157795)
1. 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]
2. 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]
3. 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]
4. Clinical course correlates poorly with muscle pathology in nemaline myopathy.
Ryan MM; Ilkovski B; Strickland CD; Schnell C; Sanoudou D; Midgett C; Houston R; Muirhead D; Dennett X; Shield LK; De Girolami U; Iannaccone ST; Laing NG; North KN; Beggs AH
Neurology; 2003 Feb; 60(4):665-73. PubMed ID: 12601110
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Myofiber adaptational response to exercise in a mouse model of nemaline myopathy.
Nair-Shalliker V; Kee AJ; Joya JE; Lucas CA; Hoh JF; Hardeman EC
Muscle Nerve; 2004 Oct; 30(4):470-80. PubMed ID: 15372535
[TBL] [Abstract][Full Text] [Related]
8. Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy.
Wattanasirichaigoon D; Swoboda KJ; Takada F; Tong HQ; Lip V; Iannaccone ST; Wallgren-Pettersson C; Laing NG; Beggs AH
Neurology; 2002 Aug; 59(4):613-7. PubMed ID: 12196661
[TBL] [Abstract][Full Text] [Related]
9. Nebulin expression in patients with nemaline myopathy.
Gurgel-Giannetti J; Reed U; Bang ML; Pelin K; Donner K; Marie SK; Carvalho M; Fireman MA; Zanoteli E; Oliveira AS; Zatz M; Wallgren-Pettersson C; Labeit S; Vainzof M
Neuromuscul Disord; 2001 Mar; 11(2):154-62. PubMed ID: 11257471
[TBL] [Abstract][Full Text] [Related]
10. A nemaline myopathy mutation in alpha-tropomyosin causes defective regulation of striated muscle force production.
Michele DE; Albayya FP; Metzger JM
J Clin Invest; 1999 Dec; 104(11):1575-81. PubMed ID: 10587521
[TBL] [Abstract][Full Text] [Related]
11. Nebulin deficiency in adult muscle causes sarcomere defects and muscle-type-dependent changes in trophicity: novel insights in nemaline myopathy.
Li F; Buck D; De Winter J; Kolb J; Meng H; Birch C; Slater R; Escobar YN; Smith JE; Yang L; Konhilas J; Lawlor MW; Ottenheijm C; Granzier HL
Hum Mol Genet; 2015 Sep; 24(18):5219-33. PubMed ID: 26123491
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Muscle weakness in respiratory and peripheral skeletal muscles in a mouse model for nebulin-based nemaline myopathy.
Joureau B; de Winter JM; Stam K; Granzier H; Ottenheijm CA
Neuromuscul Disord; 2017 Jan; 27(1):83-89. PubMed ID: 27890461
[TBL] [Abstract][Full Text] [Related]
15. Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function.
Sztal TE; Zhao M; Williams C; Oorschot V; Parslow AC; Giousoh A; Yuen M; Hall TE; Costin A; Ramm G; Bird PI; Busch-Nentwich EM; Stemple DL; Currie PD; Cooper ST; Laing NG; Nowak KJ; Bryson-Richardson RJ
Acta Neuropathol; 2015 Sep; 130(3):389-406. PubMed ID: 25931053
[TBL] [Abstract][Full Text] [Related]
16. Tropomyosin in the groove? Molecular insights into an inherited myopathy.
Chase PB
J Physiol; 2007 Jun; 581(Pt 3):889. PubMed ID: 17525111
[No Abstract] [Full Text] [Related]
17. Nemaline myopathy caused by mutations in the muscle alpha-skeletal-actin gene.
Ilkovski B; Cooper ST; Nowak K; Ryan MM; Yang N; Schnell C; Durling HJ; Roddick LG; Wilkinson I; Kornberg AJ; Collins KJ; Wallace G; Gunning P; Hardeman EC; Laing NG; North KN
Am J Hum Genet; 2001 Jun; 68(6):1333-43. PubMed ID: 11333380
[TBL] [Abstract][Full Text] [Related]
18. De novo missense mutation in a constitutively expressed exon of the slow alpha-tropomyosin gene TPM3 associated with an atypical, sporadic case of nemaline myopathy.
Durling HJ; Reilich P; Müller-Höcker J; Mendel B; Pongratz D; Wallgren-Pettersson C; Gunning P; Lochmüller H; Laing NG
Neuromuscul Disord; 2002 Dec; 12(10):947-51. PubMed ID: 12467750
[TBL] [Abstract][Full Text] [Related]
19. Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy.
Tan P; Briner J; Boltshauser E; Davis MR; Wilton SD; North K; Wallgren-Pettersson C; Laing NG
Neuromuscul Disord; 1999 Dec; 9(8):573-9. PubMed ID: 10619715
[TBL] [Abstract][Full Text] [Related]
20. Autosomal dominant nemaline myopathy: a new phenotype unlinked to previously known genetic loci.
Jeannet PY; Mittaz L; Dunand M; Lobrinus JA; Bonafe L; Kuntzer T
Neuromuscul Disord; 2007 Jan; 17(1):6-12. PubMed ID: 17157023
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]