150 related articles for article (PubMed ID: 27429059)
21. TNNT1 myopathy with novel compound heterozygous mutations.
Lee S; Eum J; Park S; Ki S; Hwang BJ; Kee Y; Chae JH
Neuromuscul Disord; 2022 Feb; 32(2):176-184. PubMed ID: 35165004
[TBL] [Abstract][Full Text] [Related]
22. TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.
Wei B; Jin JP
Gene; 2016 May; 582(1):1-13. PubMed ID: 26774798
[TBL] [Abstract][Full Text] [Related]
23. Troponin-T type 1 (TNNT1)-related nemaline myopathy: unique respiratory phenotype and muscle pathology findings.
Zambon AA; Abel F; Linnane B; O'Rourke D; Phadke R; Sewry CA; Sarkozy A; Manzur A; Muntoni F
Neuromuscul Disord; 2022 Mar; 32(3):245-254. PubMed ID: 35249790
[TBL] [Abstract][Full Text] [Related]
24. Novel TNNT1 mutation and mild nemaline myopathy phenotype in an Italian patient.
Petrucci A; Primiano G; Savarese M; Sancricca C; Udd B; Servidei S
Neuromuscul Disord; 2021 Jun; 31(6):532-538. PubMed ID: 33832840
[TBL] [Abstract][Full Text] [Related]
25. Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians.
Pellerin D; Aykanat A; Ellezam B; Troiano EC; Karamchandani J; Dicaire MJ; Petitclerc M; Robertson R; Allard-Chamard X; Brunet D; Konersman CG; Mathieu J; Warman Chardon J; Gupta VA; Beggs AH; Brais B; Chrestian N
Ann Neurol; 2020 Apr; 87(4):568-583. PubMed ID: 31970803
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. The glutamic acid-rich-long C-terminal extension of troponin T has a critical role in insect muscle functions.
Cao T; Sujkowski A; Cobb T; Wessells RJ; Jin JP
J Biol Chem; 2020 Mar; 295(12):3794-3807. PubMed ID: 32024695
[TBL] [Abstract][Full Text] [Related]
28. Aberrant splicing of an alternative exon in the Drosophila troponin-T gene affects flight muscle development.
Nongthomba U; Ansari M; Thimmaiya D; Stark M; Sparrow J
Genetics; 2007 Sep; 177(1):295-306. PubMed ID: 17603127
[TBL] [Abstract][Full Text] [Related]
29. A rare TNNT1 gene variant causing creatine kinase elevation in nemaline myopathy: c.271_273del (p.Lys91del).
Yavaş C; Doğan M; Eröz R; Türegün K
Genes Genomics; 2024 May; 46(5):613-620. PubMed ID: 38363456
[TBL] [Abstract][Full Text] [Related]
30. Evolution, Regulation, and Function of N-terminal Variable Region of Troponin T: Modulation of Muscle Contractility and Beyond.
Jin JP
Int Rev Cell Mol Biol; 2016; 321():1-28. PubMed ID: 26811285
[TBL] [Abstract][Full Text] [Related]
31. Troponin T core structure and the regulatory NH2-terminal variable region.
Biesiadecki BJ; Chong SM; Nosek TM; Jin JP
Biochemistry; 2007 Feb; 46(5):1368-79. PubMed ID: 17260966
[TBL] [Abstract][Full Text] [Related]
32. Role of the fetal and alpha/beta exons in the function of fast skeletal troponin T isoforms: correlation with altered Ca2+ regulation associated with development.
Chaudhuri T; Mukherjea M; Sachdev S; Randall JD; Sarkar S
J Mol Biol; 2005 Sep; 352(1):58-71. PubMed ID: 16081096
[TBL] [Abstract][Full Text] [Related]
33. Modulation of troponin T molecular conformation and flexibility by metal ion binding to the NH2-terminal variable region.
Jin JP; Root DD
Biochemistry; 2000 Sep; 39(38):11702-13. PubMed ID: 10995238
[TBL] [Abstract][Full Text] [Related]
34. Early Divergence of the C-Terminal Variable Region of Troponin T Via a Pair of Mutually Exclusive Alternatively Spliced Exons Followed by a Selective Fixation in Vertebrate Heart.
Cao T; Akhter S; Jin JP
J Mol Evol; 2022 Dec; 90(6):452-467. PubMed ID: 36171395
[TBL] [Abstract][Full Text] [Related]
35. Autosomal dominantly inherited myopathy likely caused by the TNNT1 variant p.(Asp65Ala).
Holling T; Lisfeld J; Johannsen J; Matschke J; Song F; Altmeppen HC; Kutsche K
Hum Mutat; 2022 Sep; 43(9):1224-1233. PubMed ID: 35510366
[TBL] [Abstract][Full Text] [Related]
36. Troponin T is essential for sarcomere assembly in zebrafish skeletal muscle.
Ferrante MI; Kiff RM; Goulding DA; Stemple DL
J Cell Sci; 2011 Feb; 124(Pt 4):565-77. PubMed ID: 21245197
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. 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]
40. Cooperative interaction between developmentally regulated troponin T and tropomyosin isoforms in the absence of F-actin.
Ogut O; Jin JP
J Biol Chem; 2000 Aug; 275(34):26089-95. PubMed ID: 10844003
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
