248 related articles for article (PubMed ID: 19209820)
1. Tropomyosins in skeletal muscle diseases.
Kee AJ; Hardeman EC
Adv Exp Med Biol; 2008; 644():143-57. PubMed ID: 19209820
[TBL] [Abstract][Full Text] [Related]
2. Thin filament proteins mutations associated with skeletal myopathies: defective regulation of muscle contraction.
Ochala J
J Mol Med (Berl); 2008 Nov; 86(11):1197-204. PubMed ID: 18574571
[TBL] [Abstract][Full Text] [Related]
3. Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies.
Marttila M; Lehtokari VL; Marston S; Nyman TA; Barnerias C; Beggs AH; Bertini E; Ceyhan-Birsoy O; Cintas P; Gerard M; Gilbert-Dussardier B; Hogue JS; Longman C; Eymard B; Frydman M; Kang PB; Klinge L; Kolski H; Lochmüller H; Magy L; Manel V; Mayer M; Mercuri E; North KN; Peudenier-Robert S; Pihko H; Probst FJ; Reisin R; Stewart W; Taratuto AL; de Visser M; Wilichowski E; Winer J; Nowak K; Laing NG; Winder TL; Monnier N; Clarke NF; Pelin K; Grönholm M; Wallgren-Pettersson C
Hum Mutat; 2014 Jul; 35(7):779-90. PubMed ID: 24692096
[TBL] [Abstract][Full Text] [Related]
4. Congenital myopathies: diseases of the actin cytoskeleton.
Clarkson E; Costa CF; Machesky LM
J Pathol; 2004 Nov; 204(4):407-17. PubMed ID: 15495263
[TBL] [Abstract][Full Text] [Related]
5. Skeletal muscle disease due to mutations in tropomyosin, troponin and cofilin.
Clarke NF
Adv Exp Med Biol; 2008; 642():40-54. PubMed ID: 19181092
[TBL] [Abstract][Full Text] [Related]
6. The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of Myopathies.
Borovikov YS; Karpicheva OE; Simonyan AO; Avrova SV; Rogozovets EA; Sirenko VV; Redwood CS
Int J Mol Sci; 2018 Dec; 19(12):. PubMed ID: 30544720
[TBL] [Abstract][Full Text] [Related]
7. [Congenital myopathies - skeletal muscle diseases related to disorder of actin filament structure and functions].
Robaszkiewicz K; Moraczewska J
Postepy Hig Med Dosw (Online); 2011 Jun; 65():347-56. PubMed ID: 21677359
[TBL] [Abstract][Full Text] [Related]
8. Autosomal dominant nemaline myopathy caused by a novel alpha-tropomyosin 3 mutation.
Kiphuth IC; Krause S; Huttner HB; Dekomien G; Struffert T; Schröder R
J Neurol; 2010 Apr; 257(4):658-60. PubMed ID: 20012312
[TBL] [Abstract][Full Text] [Related]
9. Demonstration of beta-tropomyosin (Tpm2) and duplication of the alpha-slow tropomyosin gene (TPM3) in Atlantic salmon Salmo salar.
Silva AMM; Kennedy LS; Hasan SC; Cohen AM; Heeley DH
Comp Biochem Physiol B Biochem Mol Biol; 2020 Jul; 245():110439. PubMed ID: 32283206
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Nebulin interactions with actin and tropomyosin are altered by disease-causing mutations.
Marttila M; Hanif M; Lemola E; Nowak KJ; Laitila J; Grönholm M; Wallgren-Pettersson C; Pelin K
Skelet Muscle; 2014; 4():15. PubMed ID: 25110572
[TBL] [Abstract][Full Text] [Related]
12. Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients.
Marston S; Memo M; Messer A; Papadaki M; Nowak K; McNamara E; Ong R; El-Mezgueldi M; Li X; Lehman W
Hum Mol Genet; 2013 Dec; 22(24):4978-87. PubMed ID: 23886664
[TBL] [Abstract][Full Text] [Related]
13. Myopathy-causing Q147P TPM2 mutation shifts tropomyosin strands further towards the open position and increases the proportion of strong-binding cross-bridges during the ATPase cycle.
Karpicheva OE; Simonyan AO; Kuleva NV; Redwood CS; Borovikov YS
Biochim Biophys Acta; 2016 Mar; 1864(3):260-267. PubMed ID: 26708479
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Frequency and phenotype of patients carrying TPM2 and TPM3 gene mutations in a cohort of 94 patients with congenital myopathy.
Citirak G; Witting N; Duno M; Werlauff U; Petri H; Vissing J
Neuromuscul Disord; 2014 Apr; 24(4):325-30. PubMed ID: 24507666
[TBL] [Abstract][Full Text] [Related]
17. Tropomyosin isoforms differentially modulate the regulation of actin filament polymerization and depolymerization by cofilins.
Robaszkiewicz K; Ostrowska Z; Marchlewicz K; Moraczewska J
FEBS J; 2016 Feb; 283(4):723-37. PubMed ID: 26663234
[TBL] [Abstract][Full Text] [Related]
18. Mutations Q93H and E97K in
Śliwinska M; Robaszkiewicz K; Wasąg P; Moraczewska J
Int J Mol Sci; 2021 Apr; 22(8):. PubMed ID: 33919826
[TBL] [Abstract][Full Text] [Related]
19. Cap disease due to mutation of the beta-tropomyosin gene (TPM2).
Clarke NF; Domazetovska A; Waddell L; Kornberg A; McLean C; North KN
Neuromuscul Disord; 2009 May; 19(5):348-51. PubMed ID: 19345583
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]