TNNT3


TNNT3

Troponin T type 3 (skeletal, fast), also known as TNNT3, is a human gene.cite web | title = Entrez Gene: TNNT3 troponin T type 3 (skeletal, fast)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7140| accessdate = ]

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References

Further reading

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*cite journal | author=Chong PC, Hodges RS |title=Photochemical cross-linking between rabbit skeletal troponin subunits. Troponin I-troponin T interactions. |journal=J. Biol. Chem. |volume=257 |issue= 19 |pages= 11667–72 |year= 1982 |pmid= 7118902 |doi=
*cite journal | author=Briggs MM, Maready M, Schmidt JM, Schachat F |title=Identification of a fetal exon in the human fast troponin T gene. |journal=FEBS Lett. |volume=350 |issue= 1 |pages= 37–40 |year= 1994 |pmid= 8062920 |doi=
*cite journal | author=Wu QL, Jha PK, Raychowdhury MK, "et al." |title=Isolation and characterization of human fast skeletal beta troponin T cDNA: comparative sequence analysis of isoforms and insight into the evolution of members of a multigene family. |journal=DNA Cell Biol. |volume=13 |issue= 3 |pages= 217–33 |year= 1994 |pmid= 8172653 |doi=
*cite journal | author=Mao C, Baumgartner AP, Jha PK, "et al." |title=Assignment of the human fast skeletal troponin T gene (TNNT3) to chromosome 11p15.5: evidence for the presence of 11pter in a monochromosome 9 somatic cell hybrid in NIGMS mapping panel 2. |journal=Genomics |volume=31 |issue= 3 |pages= 385–8 |year= 1997 |pmid= 8838323 |doi= 10.1006/geno.1996.0064
*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=Krakowiak PA, O'Quinn JR, Bohnsack JF, "et al." |title=A variant of Freeman-Sheldon syndrome maps to 11p15.5-pter. |journal=Am. J. Hum. Genet. |volume=60 |issue= 2 |pages= 426–32 |year= 1997 |pmid= 9012416 |doi=
*cite journal | author=Krakowiak PA, Bohnsack JF, Carey JC, Bamshad M |title=Clinical analysis of a variant of Freeman-Sheldon syndrome (DA2B). |journal=Am. J. Med. Genet. |volume=76 |issue= 1 |pages= 93–8 |year= 1998 |pmid= 9508073 |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
*cite journal | author=Hsiao CD, Tsai WY, Horng LS, Tsai HJ |title=Molecular structure and developmental expression of three muscle-type troponin T genes in zebrafish. |journal=Dev. Dyn. |volume=227 |issue= 2 |pages= 266–79 |year= 2004 |pmid= 12761854 |doi= 10.1002/dvdy.10305
*cite journal | author=Sung SS, Brassington AM, Krakowiak PA, "et al." |title=Mutations in TNNT3 cause multiple congenital contractures: a second locus for distal arthrogryposis type 2B. |journal=Am. J. Hum. Genet. |volume=73 |issue= 1 |pages= 212–4 |year= 2003 |pmid= 12865991 |doi= 10.1086/376418
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Witt SH, Granzier H, Witt CC, Labeit S |title=MURF-1 and MURF-2 target a specific subset of myofibrillar proteins redundantly: towards understanding MURF-dependent muscle ubiquitination. |journal=J. Mol. Biol. |volume=350 |issue= 4 |pages= 713–22 |year= 2005 |pmid= 15967462 |doi= 10.1016/j.jmb.2005.05.021
*cite journal | author=Chaudhuri T, Mukherjea M, Sachdev S, "et al." |title=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. |journal=J. Mol. Biol. |volume=352 |issue= 1 |pages= 58–71 |year= 2005 |pmid= 16081096 |doi= 10.1016/j.jmb.2005.06.066
*cite journal | author=Stelzl U, Worm U, Lalowski M, "et al." |title=A human protein-protein interaction network: a resource for annotating the proteome. |journal=Cell |volume=122 |issue= 6 |pages= 957–68 |year= 2005 |pmid= 16169070 |doi= 10.1016/j.cell.2005.08.029
*cite journal | author=Kimura K, Wakamatsu A, Suzuki Y, "et al." |title=Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. |journal=Genome Res. |volume=16 |issue= 1 |pages= 55–65 |year= 2006 |pmid= 16344560 |doi= 10.1101/gr.4039406

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Look at other dictionaries:

  • Troponina T — tipo 1 (músculo esquelético 1, lenta) HUGO 11948 Símbolo TNNT1 Símbolos alt. ANM, STNT, TNT, TNTS, FLJ98147, M …   Wikipedia Español

  • Freeman-Sheldon syndrome — Infobox Disease Name = Freeman Sheldon syndrome Caption = DiseasesDB = 31817 ICD10 = ICD9 = ICD9|759.89 ICDO = OMIM = 193700 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Freeman Sheldon syndrome (FSS), also termed distal arthrogryposis …   Wikipedia

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  • Freeman–Sheldon syndrome — Freeman Sheldon syndrome Classification and external resources ICD 9 759.89 …   Wikipedia


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