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.
191 related articles for article (PubMed ID: 25268244)
21. Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation. Moraczewska J; Greenfield NJ; Liu Y; Hitchcock-DeGregori SE Biophys J; 2000 Dec; 79(6):3217-25. PubMed ID: 11106625 [TBL] [Abstract][Full Text] [Related]
22. A Novel Variant in Robaszkiewicz K; Siatkowska M; Wadman RI; Kamsteeg EJ; Chen Z; Merve A; Parton M; Bugiardini E; de Bie C; Moraczewska J Int J Mol Sci; 2023 Nov; 24(22):. PubMed ID: 38003336 [TBL] [Abstract][Full Text] [Related]
23. Skeletal muscle of mice with a mutation in slow alpha-tropomyosin is weaker at lower lengths. de Haan A; van der Vliet MR; Gommans IM; Hardeman EC; van Engelen BG Neuromuscul Disord; 2002 Dec; 12(10):952-7. PubMed ID: 12467751 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy. Ottenheijm CA; Buck D; de Winter JM; Ferrara C; Piroddi N; Tesi C; Jasper JR; Malik FI; Meng H; Stienen GJ; Beggs AH; Labeit S; Poggesi C; Lawlor MW; Granzier H Brain; 2013 Jun; 136(Pt 6):1718-31. PubMed ID: 23715096 [TBL] [Abstract][Full Text] [Related]
26. Variants in tropomyosins TPM2 and TPM3 causing muscle hypertonia. Wallgren-Pettersson C; Jokela M; Lehtokari VL; Tyynismaa H; Sainio MT; Ylikallio E; Tynninen O; Pelin K; Auranen M Neuromuscul Disord; 2024 Feb; 35():29-32. PubMed ID: 38219297 [TBL] [Abstract][Full Text] [Related]
27. Mild phenotype of nemaline myopathy with sleep hypoventilation due to a mutation in the skeletal muscle alpha-actin (ACTA1) gene. Jungbluth H; Sewry CA; Brown SC; Nowak KJ; Laing NG; Wallgren-Pettersson C; Pelin K; Manzur AY; Mercuri E; Dubowitz V; Muntoni F Neuromuscul Disord; 2001 Jan; 11(1):35-40. PubMed ID: 11166164 [TBL] [Abstract][Full Text] [Related]
28. Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion. Lawlor MW; Dechene ET; Roumm E; Geggel AS; Moghadaszadeh B; Beggs AH Hum Mutat; 2010 Feb; 31(2):176-83. PubMed ID: 19953533 [TBL] [Abstract][Full Text] [Related]
29. Novel Compound Heterozygous Splice-Site Variants in TPM3 Revealed by RNA Sequencing in a Patient with an Unusual Form of Nemaline Myopathy: A Case Report. Pelin K; Sagath L; Lehtonen J; Kiiski K; Tynninen O; Paetau A; Johari M; Savarese M; Wallgren-Pettersson C; Lehtokari VL J Neuromuscul Dis; 2023; 10(5):977-984. PubMed ID: 37393515 [TBL] [Abstract][Full Text] [Related]
33. K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity. Mokbel N; Ilkovski B; Kreissl M; Memo M; Jeffries CM; Marttila M; Lehtokari VL; Lemola E; Grönholm M; Yang N; Menard D; Marcorelles P; Echaniz-Laguna A; Reimann J; Vainzof M; Monnier N; Ravenscroft G; McNamara E; Nowak KJ; Laing NG; Wallgren-Pettersson C; Trewhella J; Marston S; Ottenheijm C; North KN; Clarke NF Brain; 2013 Feb; 136(Pt 2):494-507. PubMed ID: 23378224 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. 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]
36. Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy. Donner K; Ollikainen M; Ridanpää M; Christen HJ; Goebel HH; de Visser M; Pelin K; Wallgren-Pettersson C Neuromuscul Disord; 2002 Feb; 12(2):151-8. PubMed ID: 11738357 [TBL] [Abstract][Full Text] [Related]
37. A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: a clinical and pathological study. Pénisson-Besnier I; Monnier N; Toutain A; Dubas F; Laing N Neuromuscul Disord; 2007 Apr; 17(4):330-7. PubMed ID: 17376686 [TBL] [Abstract][Full Text] [Related]
40. Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2). Tajsharghi H; Ohlsson M; Lindberg C; Oldfors A Arch Neurol; 2007 Sep; 64(9):1334-8. PubMed ID: 17846275 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]