| 1 | NEM5, TNNT1
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| Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.
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| Konersman CG, Freyermuth F, Winder TL, Lawlor MW, Lagier-Tourenne C, Patel SB.
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| Mol Genet Genomic Med 5(6):678-691. doi: 10.1002/mgg3.325. Epub 2017 Aug 21.
2017
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| 2 | NEM5, TNNT1
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| Protein Structure-Function Relationship at Work: Learning from Myopathy Mutations of the Slow Skeletal Muscle Isoform of Troponin T.
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| Mondal A, Jin JP.
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| Front Physiol 7:449. eCollection 2016. Review.
2016
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| 3 | TNNT1, TNNT2, TNNT3
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| TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships.
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| Wei B, Jin JP.
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| Gene 582(1):1-13. doi: 10.1016/j.gene.2016.01.006. Epub 2016 Jan 13. Review.
2016
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| 4 | TNNT1
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| Deficiency of slow skeletal muscle troponin T causes atrophy of type I slow fibres and decreases tolerance to fatigue.
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| Wei B, Lu Y, Jin JP.
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| J Physiol 592(6):1367-80. doi: 10.1113/jphysiol.2013.268177. Epub 2014 Jan 20.
2014
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| 5 | TNNT1
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| The functional properties of human slow skeletal troponin T isoforms in cardiac muscle regulation.
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| Pinto JR, Gomes AV, Jones MA, Liang J, Nguyen S, Miller T, Parvatiyar MS, Potter JD.
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| J Biol Chem 287(44):37362-70. doi: 10.1074/jbc.M112.364927. Epub 2012 Sep 12.
2012
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| 6 | TNNT1
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| Serum levels of high-sensitivity troponin T: a novel marker for cardiac remodeling in hypertrophic cardiomyopathy.
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| Moreno V, Hernández-Romero D, Vilchez JA, García-Honrubia A, Cambronero F, Casas T, González J, Martínez P, Climent V, de la Morena G, Valdés M, Marín F.
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| J Card Fail 16(12):950-6. doi: 10.1016/j.cardfail.2010.07.245.
2010
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| 7 | GATA4, TNNT1, ZFPM2
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| Cardiac expression of Tnnt1 requires the GATA4-FOG2 transcription complex.
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| Manuylov NL, Tevosian SG.
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| ScientificWorldJournal 9:575-87. doi: 10.1100/tsw.2009.75.
2009
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| 8 | TNNT1
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| The expression of Troponin T1 gene is induced by ketamine in adult mouse brain.
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| Lowe XR, Lu X, Marchetti F, Wyrobek AJ.
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| Brain Res 1174:7-17. Epub 2007 Aug 2.
2007
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| 9 | NEM5,TNNT1
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| Cellular fate of truncated slow skeletal muscle troponin T produced by Glu180 nonsense mutation in amish nemaline myopathy.
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| Wang X, Huang QQ, Breckenridge MT, Chen A, Crawford TO, Morton DH, Jin JP.
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| J Biol Chem 280(14):13241-9. Epub 2005 Jan 23. 2005
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| 10 | NEM5, TNNT1
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| A novel nemaline myopathy in the Amish caused by a mutation in troponin T1.
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| Johnston JJ, Kelley RI, Crawford TO, Morton DH, Agarwala R, Koch T, Schaffer AA, Francomano CA, Biesecker LG.
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| Am J Hum Genet 67(4):814-21. 2000
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| 11 | TNNI1, TNNI3, TNNT1, TNNT2
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| Close physical linkage of human troponin genes: organization, sequence, and expression of the locus encoding cardiac troponin I and slow skeletal troponin T.
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| Barton PJ, et al.
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| Genomics 57(1):102-9 1999
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| 12 | TNNT1
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| A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single gene.
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| Samson F, et al.
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| Biochem Biophys Res Commun 199 : 841-847. 1994
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| 13 | TNNT1
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| Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reaction.
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| Novelli G, et al.
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| Hum Genet 88 : 697-698. 1992
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| 14 | TNNT1
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| Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis.
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| Samson F, et al.
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| Genomics 13 : 1374-1375. 1992
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| 15 | TNNT1
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| Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscle.
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| Novelli G, et al.
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| Cell Biochem Funct 10 : 251-256. 1992
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| 16 | TNNT1
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| Isolation and mapping of the slow skeletal troponin T using the polymerase chain reaction.
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| Novelli G, et al.
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| (HGM11) Cytogenet Cell Genet 58 : 2023. 1991
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| 17 | TNNT1
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| A PstI polymorphism detected by a genomic clone at the human slow troponin T (TNNT1) gene locus.
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| Samson F, et al.
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| Nucleic Acids Res 19 : 6058. 1991
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| 18 | TNNT1
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| Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNA.
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| Samson F, et al.
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| J Neurosci Res 27 : 441-451. 1990
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| 19 | TNNT1
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| Alternative splicing generates variants in important functional domains of human slow skeletal troponin T.
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| Gahlmann R, Troutt AB, Wade RP, Gunning P, Kedes L.
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| J Biol Chem 262(33):16122-6. 1987
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