[cite web | title = Entrez Gene: TNNT1 troponin T type 1 (skeletal, slow)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7138| accessdate = ] ] PBB_Summary
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References
Further reading
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*cite journal | author=Nadal-Ginard B, Mahdavi V |title=Molecular basis of cardiac performance. Plasticity of the myocardium generated through protein isoform switches. |journal=J. Clin. Invest. |volume=84 |issue= 6 |pages= 1693–700 |year= 1990 |pmid= 2687327 |doi=
*cite journal | author=Wu AH, Ford L |title=Release of cardiac troponin in acute coronary syndromes: ischemia or necrosis? |journal=Clin. Chim. Acta |volume=284 |issue= 2 |pages= 161–74 |year= 1999 |pmid= 10451243 |doi=
*cite journal | author=Novelli G, Gennarelli M, Zelano G, "et al." |title=Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscle. |journal=Cell Biochem. Funct. |volume=10 |issue= 4 |pages= 251–6 |year= 1993 |pmid= 1473264 |doi= 10.1002/cbf.290100407
*cite journal | author=Samson F, de Jong PJ, Trask BJ, "et al." |title=Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis. |journal=Genomics |volume=13 |issue= 4 |pages= 1374–5 |year= 1992 |pmid= 1505979 |doi=
*cite journal | author=Gahlmann R, Troutt AB, Wade RP, "et al." |title=Alternative splicing generates variants in important functional domains of human slow skeletal troponin T. |journal=J. Biol. Chem. |volume=262 |issue= 33 |pages= 16122–6 |year= 1987 |pmid= 2824479 |doi=
*cite journal | author=Heeley DH, Golosinska K, Smillie LB |title=The effects of troponin T fragments T1 and T2 on the binding of nonpolymerizable tropomyosin to F-actin in the presence and absence of troponin I and troponin C. |journal=J. Biol. Chem. |volume=262 |issue= 21 |pages= 9971–8 |year= 1987 |pmid= 3611073 |doi=
*cite journal | author=Pearlstone JR, Smillie LB |title=Effects of troponin-I plus-C on the binding of troponin-T and its fragments to alpha-tropomyosin. Ca2+ sensitivity and cooperativity. |journal=J. Biol. Chem. |volume=258 |issue= 4 |pages= 2534–42 |year= 1983 |pmid= 6822572 |doi=
*cite journal | author=Samson F, Mesnard L, Mihovilovic M, "et al." |title=A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single gene. |journal=Biochem. Biophys. Res. Commun. |volume=199 |issue= 2 |pages= 841–7 |year= 1994 |pmid= 8135831 |doi= 10.1006/bbrc.1994.1305
*cite journal | author=Novelli G, Gennarelli M, Sangiuolo F, "et al." |title=Isolation and cloning by a polymerase chain reaction of a genomic DNA fragment of the human slow skeletal troponin (TNNT1) gene. |journal=Cell Biochem. Funct. |volume=11 |issue= 3 |pages= 187–91 |year= 1993 |pmid= 8403232 |doi= 10.1002/cbf.290110306
*cite journal | author=Jha PK, Leavis PC, Sarkar S |title=Interaction of deletion mutants of troponins I and T: COOH-terminal truncation of troponin T abolishes troponin I binding and reduces Ca2+ sensitivity of the reconstituted regulatory system. |journal=Biochemistry |volume=35 |issue= 51 |pages= 16573–80 |year= 1997 |pmid= 8987992 |doi= 10.1021/bi9622433
*cite journal | author=Stefancsik R, Jha PK, Sarkar S |title=Identification and mutagenesis of a highly conserved domain in troponin T responsible for troponin I binding: potential role for coiled coil interaction. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 3 |pages= 957–62 |year= 1998 |pmid= 9448267 |doi=
*cite journal | author=Jha PK, Sarkar S |title=A recombinant monocysteine mutant (Ser to Cys-155) of fast skeletal troponin T: identification by cross-linking of a domain involved in a physiologically relevant interaction with troponins C and I. |journal=Biochemistry |volume=37 |issue= 35 |pages= 12253–60 |year= 1998 |pmid= 9724539 |doi= 10.1021/bi980025z
*cite journal | author=Barton PJ, Cullen ME, Townsend PJ, "et al." |title=Close physical linkage of human troponin genes: organization, sequence, and expression of the locus encoding cardiac troponin I and slow skeletal troponin T. |journal=Genomics |volume=57 |issue= 1 |pages= 102–9 |year= 1999 |pmid= 10191089 |doi= 10.1006/geno.1998.5702
*cite journal | author=Mukherjea P, Tong L, Seidman JG, "et al." |title=Altered regulatory function of two familial hypertrophic cardiomyopathy troponin T mutants. |journal=Biochemistry |volume=38 |issue= 40 |pages= 13296–301 |year= 1999 |pmid= 10529204 |doi=
*cite journal | author=Yuasa K, Michibata H, Omori K, Yanaka N |title=A novel interaction of cGMP-dependent protein kinase I with troponin T. |journal=J. Biol. Chem. |volume=274 |issue= 52 |pages= 37429–34 |year= 2000 |pmid= 10601315 |doi=
*cite journal | author=Johnston JJ, Kelley RI, Crawford TO, "et al." |title=A novel nemaline myopathy in the Amish caused by a mutation in troponin T1. |journal=Am. J. Hum. Genet. |volume=67 |issue= 4 |pages= 814–21 |year= 2000 |pmid= 10952871 |doi=
*cite journal | author=Schmidtmann A, Lohmann K, Jaquet K |title=The interaction of the bisphosphorylated N-terminal arm of cardiac troponin I-A 31P-NMR study. |journal=FEBS Lett. |volume=513 |issue= 2-3 |pages= 289–93 |year= 2002 |pmid= 11904166 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
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