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1 to 25 of 285  Show
  1. 1
    "Homo sapiens cardiac troponin T (TNNT2) gene intron 13 (partial) and exon 14."
    Bahl A., Kubo T., Steffensen U., Steffensen M., McKenna W.J., Mogensen J.
    Submitted (OCT-2002) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE.
    Category: Sequences.
    Tissue: Blood.
    Source: UniProtKB/TrEMBL (unreviewed).
  2. 2
    Nallari P., Sikindlapuram A.
    Submitted (AUG-2007) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE.
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).
  3. 3
    "Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathy."
    Cuda G., Mussari A., Concolino D., Costanzo F.S., Strisciuglio P.
    Hum. Mutat. 19:309-310(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: Frataxin and cardiac troponin T gene mutations co-exist in a child with Friedreich ataxia and familial hypertrophic cardiomyopathy.Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 15 other entries.

  4. 4
    "Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin T genes in hypertrophic cardiomyopathy: a comprehensive outpatient perspective."
    Ackerman M.J., VanDriest S.L., Ommen S.R., Will M.L., Nishimura R.A., Tajik A.J., Gersh B.J.
    J. Am. Coll. Cardiol. 39:2042-2048(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 31 other entries.

  5. 5
    "Prevalence and severity of "benign" mutations in the beta-myosin heavy chain, cardiac troponin T, and alpha-tropomyosin genes in hypertrophic cardiomyopathy."
    Van Driest S.L., Ackerman M.J., Ommen S.R., Shakur R., Will M.L., Nishimura R.A., Tajik A.J., Gersh B.J.
    Circulation 106:3085-3090(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 52 other entries.

  6. 6
    "Truncation by Glu180 nonsense mutation results in complete loss of slow skeletal muscle troponin T in a lethal nemaline myopathy."
    Jin J.P., Brotto M.A., Hossain M.M., Huang Q.Q., Brotto L.S., Nosek T.M., Morton D.H., Crawford T.O.
    J. Biol. Chem. 278:26159-26165(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: functional slow skeletal muscle troponin T requires a full non-truncated sequence including the COOH-terminal domainImported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  7. 7
    "The diagnostic value of troponin T and myoglobin levels in acute myocardial infarction: a study in Turkish patients."
    Vatansever S., Akkaya V., Erk O., Ozturk S., Karan M.A., Salmayenli N., Tascioglu C., Guler K.
    J. Int. Med. Res. 31:76-83(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: It was concluded that myoglobin levels on admission and TnT at 2 h had the greatest diagnostic rate for myocardial infarction.Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 19 other entries.

  8. 8
    "ASK1 associates with troponin T and induces troponin T phosphorylation and contractile dysfunction in cardiomyocytes."
    He X., Liu Y., Sharma V., Dirksen R.T., Waugh R., Sheu S.S., Min W.
    Am. J. Pathol. 163:243-251(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: Data suggest that apoptosis signal-regulating kinase 1 plays an important role in regulation of cardiac contractile function by phosphorylating cardiac troponin T2.Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  9. 9
    "Different functional properties of troponin T mutants that cause dilated cardiomyopathy."
    Venkatraman G., Harada K., Gomes A.V., Kerrick W.G., Potter J.D.
    J. Biol. Chem. 278:41670-41676(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: effects of Troponin T (TnT) mutants R141W and DeltaK210 on the Ca2+ sensitivity of force development in cardiac fibers and maximal ATPase activityImported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  10. 10
    "Prevalence and clinical profile of troponin T mutations among patients with hypertrophic cardiomyopathy in tuscany."
    Torricelli F., Girolami F., Olivotto I., Passerini I., Frusconi S., Vargiu D., Richard P., Cecchi F.
    Am. J. Cardiol. 92:1358-1362(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  11. 11
    "Familial hypertrophic cardiomyopathy mutations from different functional regions of troponin T result in different effects on the pH and Ca2+ sensitivity of cardiac muscle contraction."
    Harada K., Potter J.D.
    J. Biol. Chem. 279:14488-14495(2004) [PubMed] [Europe PMC] [Abstract]
    Annotation: different regions of TnT may contribute to the pathogenesis of TnT-linked Familial hypertrophic cardiomyopathy through different mechanismsImported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  12. 12
    "The role of a common TNNT2 polymorphism in cardiac hypertrophy."
    Komamura K., Iwai N., Kokame K., Yasumura Y., Kim J., Yamagishi M., Morisaki T., Kimura A., Tomoike H., Kitakaze M., Miyatake K.
    J. Hum. Genet. 49:129-133(2004) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: TNNT2 deletion allele could be associated with a predisposition to prominent left ventricular hypertrophy; Observational study of gene-disease association. (HuGE Navigator)Imported, Associated with CARDIOVASCULAR: left ventricular hypertrophy.Imported.
    Source: GeneRIF:7139, GAD:137096.

    This publication is mapped to 11 other entries.

  13. 13
    "Usefulness of rapid quantitative measurement of myoglobin and troponin T in early diagnosis of acute myocardial infarction."
    Yamamoto M., Komiyama N., Koizumi T., Nameki M., Yamamoto Y., Toyoda T., Okuno T., Tateno K., Sano K., Himi T., Kuriyama N., Namikawa S., Yokoyama M., Komuro I.
    Circ. J. 68:639-644(2004) [PubMed] [Europe PMC] [Abstract]
    Annotation: Quantitative test is useful for early diagnosis of acute myocardial infarct and as an indicator of its severity.Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 19 other entries.

  14. 14
    "[A novel missense mutation, K124N, in the troponin T gene of Chinese populations with hypertrophic cardiomyopathy]."
    An F.S., Zhang Y., Li D.Q., Yang X.S., Li L., Zhang C., Yan M.L., Wang Y., An G.P.
    Zhonghua Yi Xue Za Zhi 84:1340-1343(2004) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Associated with CARDIOVASCULAR: cardiomyopathy.Imported, Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GAD:137098, GeneRIF:7139.

    This publication is mapped to 11 other entries.

  15. 15
    "The slow skeletal muscle troponin T gene is expressed in developing and diseased human heart."
    Barton P.J., Felkin L.E., Koban M.U., Cullen M.E., Brand N.J., Dhoot G.K.
    Mol. Cell. Biochem. 263:91-97(2004) [PubMed] [Europe PMC] [Abstract]
    Annotation: slow skeletal TnT mRNA is readily detectable during early human heart developmentImported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  16. 16
    "Role of troponin T in disease."
    Gomes A.V., Barnes J.A., Harada K., Potter J.D.
    Mol. Cell. Biochem. 263:115-129(2004) [PubMed] [Europe PMC] [Abstract]
    Annotation: Role of TnT in muscle physiology and disease. Review.Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  17. 17
    "Mutations profile in Chinese patients with hypertrophic cardiomyopathy."
    Song L., Zou Y., Wang J., Wang Z., Zhen Y., Lou K., Zhang Q., Wang X., Wang H., Li J., Hui R.
    Clin. Chim. Acta 351:209-216(2005) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:7139.

    This publication is cited by 2 and mapped to 43 other entries.

  18. 18
    "The Delta 14 mutation of human cardiac troponin T enhances ATPase activity and alters the cooperative binding of S1-ADP to regulated actin."
    Gafurov B., Fredricksen S., Cai A., Brenner B., Chase P.B., Chalovich J.M.
    Biochemistry 43:15276-15285(2004) [PubMed] [Europe PMC] [Abstract]
    Annotation: Evidence is shown that the Delta14 mutation of troponin T as seen in some cases of familial hypertrophic cardiomyopathy results in stabilization of regulated actin in a more active state.Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  19. 19
    "Cardiac troponins and N-terminal pro-brain natriuretic peptide in acute ischemic stroke do not relate to clinical prognosis."
    Etgen T., Baum H., Sander K., Sander D.
    Stroke 36:270-275(2005) [PubMed] [Europe PMC] [Abstract]
    Annotation: NT-proBNP cTnT or cTnI do not have roles in acute ischemic stroke when other risk factors are consideredImported.
    Source: GeneRIF:7139.

    This publication is mapped to 23 other entries.

  20. 20
    "Serum cardiac troponin T levels as an indicator of myocardial injury in ischemic and hemorrhagic stroke patients."
    Apak I., Iltumur K., Tamam Y., Kaya N.
    Tohoku J. Exp. Med. 205:93-101(2005) [PubMed] [Europe PMC] [Abstract]
    Annotation: Measurement of the serum levels of cTnT is of clinical importance in evaluating myocardial injuryImported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  21. 21
    "Modality of brain death and serum troponin T levels in donors and their heart transplant recipients."
    Hokl J., Cerny J., Nemec P., Studenik P., Kuzmova I., Vespalec J.
    Ann. Transplant. 9:42-43(2004) [PubMed] [Europe PMC] [Abstract]
    Annotation: No differences in troponin T or inotropic support levels found in relation to modality of organ donors' brain death.Imported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  22. 22
    "Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene."
    Villard E., Duboscq-Bidot L., Charron P., Benaiche A., Conraads V., Sylvius N., Komajda M.
    Eur. Heart J. 26:794-803(2005) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Associated with CARDIOVASCULAR: cardiomyopathy.Imported, Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GAD:137100, GeneRIF:7139.

    This publication is cited by 1 and mapped to 29 other entries.

  23. 23
    "Cardiac troponin T (cTnT) in hemodialysis patients with asymptomatic and symptomatic atherosclerosis."
    Hojs R., Ekart R., Hojs Fabjan T., Balon B.P., Gorenjak M.
    Arch. Med. Res. 36:367-371(2005) [PubMed] [Europe PMC] [Abstract]
    Annotation: Cardiac troponin T may have a role in progression of atherosclerosisImported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  24. 24
    "F110I and R278C troponin T mutations that cause familial hypertrophic cardiomyopathy affect muscle contraction in transgenic mice and reconstituted human cardiac fibers."
    Hernandez O.M., Szczesna-Cordary D., Knollmann B.C., Miller T., Bell M., Zhao J., Sirenko S.G., Diaz Z., Guzman G., Xu Y., Wang Y., Kerrick W.G., Potter J.D.
    J. Biol. Chem. 280:37183-37194(2005) [PubMed] [Europe PMC] [Abstract]
    Annotation: Troponin T mutations that cause familial hypertrophic cardiomyopathy affect muscle contraction in transgenic mice and reconstituted human cardiac fibersImported.
    Source: GeneRIF:7139.

    This publication is mapped to 11 other entries.

  25. 25
    "Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling."
    Ingles J., Doolan A., Chiu C., Seidman J., Seidman C., Semsarian C.
    J. Med. Genet. 42:E59-E59(2005) [PubMed] [Europe PMC] [Abstract]
    Annotation: Observational study of gene-disease association. (HuGE Navigator)Imported.
    Source: GeneRIF:7139.

    This publication is cited by 3 and mapped to 65 other entries.

1 to 25 of 285  Show