| 1 | TPM3
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| Proteomic analysis indicates the importance of TPM3 in esophageal squamous cell carcinoma invasion and metastasis.
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| Yu SB, Gao Q, Lin WW, Kang MQ.
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| Mol Med Rep 15(3):1236-1242. doi: 10.3892/mmr.2017.6145. Epub 2017 Jan 25.
2017
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| 2 | TPM3
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| TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype.
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| Donkervoort S, Papadaki M, de Winter JM, Neu MB, Kirschner J, Bolduc V, Yang ML, Gibbons MA, Hu Y, Dastgir J, Leach ME, Rutkowski A, Foley AR, Krüger M, Wartchow EP, McNamara E, Ong R, Nowak KJ, Laing NG, Clarke NF, Ottenheijm C, Marston SB, Bönnemann CG.
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| Ann Neurol 78(6):982-994. doi: 10.1002/ana.24535. Epub 2015 Nov 13.
2015
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| 3 | CFTD3, TPM3
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| Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres.
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| Yuen M, Cooper ST, Marston SB, Nowak KJ, McNamara E, Mokbel N, Ilkovski B, Ravenscroft G, Rendu J, de Winter JM, Klinge L, Beggs AH, North KN, Ottenheijm CA, Clarke NF.
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| Hum Mol Genet 24(22):6278-92. doi: 10.1093/hmg/ddv334. Epub 2015 Aug 24.
2015
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| 4 | TPM3
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| Oncogenic TPM3-ALK activation requires dimerization through the coiled-coil structure of TPM3.
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| Amano Y, Ishikawa R, Sakatani T, Ichinose J, Sunohara M, Watanabe K, Kage H, Nakajima J, Nagase T, Ohishi N, Takai D.
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| Biochem Biophys Res Commun 457(3):457-60. doi: 10.1016/j.bbrc.2015.01.014. Epub 2015 Jan 14.
2015
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| 5 | TPM3
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| Non-muscle tropomyosin (Tpm3) is crucial for asymmetric cell division and maintenance of cortical integrity in mouse oocytes.
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| Jang WI, Jo YJ, Kim HC, Jia JL, Namgoong S, Kim NH.
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| Cell Cycle 13(15):2359-69. doi: 10.4161/cc.29333.
2014
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| 6 | NEM1, NEM4, TPM2, TPM3
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| Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies.
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| Marttila M, Lehtokari VL, Marston S, Nyman TA, Barnerias C, Beggs AH, Bertini E, Ceyhan-Birsoy O, Cintas P, Gerard M, Gilbert-Dussardier B, Hogue JS, Longman C, Eymard B, Frydman M, Kang PB, Klinge L, Kolski H, Lochmüller H, Magy L, Manel V, Mayer M, Mercuri E, North KN, Peudenier-Robert S, Pihko H, Probst FJ, Reisin R, Stewart W, Taratuto AL, de Visser M, Wilichowski E, Winer J, Nowak K, Laing NG, Winder TL, Monnier N, Clarke NF, Pelin K, Grönholm M, Wallgren-Pettersson C.
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| Hum Mutat 35(7):779-90. doi: 10.1002/humu.22554. Epub 2014 May 1.
2014
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| 7 | NEM1, TPM3
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| Novel TPM3 mutation in a family with cap myopathy and review of the literature.
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| Schreckenbach T, Schröder JM, Voit T, Abicht A, Neuen-Jacob E, Roos A, Bulst S, Kuhl C, Schulz JB, Weis J, Claeys KG.
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| Neuromuscul Disord 24(2):117-24. doi: 10.1016/j.nmd.2013.10.002. Epub 2013 Oct 23. Review. 2014
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| 8 | TPM3
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| Tropomyosin regulates cell migration during skin wound healing.
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| Lees JG, Ching YW, Adams DH, Bach CT, Samuel MS, Kee AJ, Hardeman EC, Gunning P, Cowin AJ, O'Neill GM.
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| J Invest Dermatol 133(5):1330-9. doi: 10.1038/jid.2012.489. Epub 2013 Jan 10.
2013
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| 9 | STOML2, TMOD3, TPM3
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| Identification and validation of novel serum markers for early diagnosis of endometriosis.
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| Gajbhiye R, Sonawani A, Khan S, Suryawanshi A, Kadam S, Warty N, Raut V, Khole V.
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| Hum Reprod 27(2):408-17. doi: 10.1093/humrep/der410. Epub 2011 Dec 8.
2012
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| 10 | NEM1, NEM4, TPM2, TPM3
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| Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms.
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| Ochala J, Gokhin DS, Pénisson-Besnier I, Quijano-Roy S, Monnier N, Lunardi J, Romero NB, Fowler VM.
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| Hum Mol Genet 21(20):4473-85. Epub 2012 Jul 13.
2012
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| 11 | TPM1, TPM3
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| Functional structure of the promoter regions for the predominant low molecular weight isoforms of tropomyosin in human kidney cells.
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| Savill SA, Leitch HF, Harvey JN, Thomas TH.
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| J Cell Biochem 113(11):3576-86. doi: 10.1002/jcb.24236.
2012
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| 12 | TPM3
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| Tropomyosin isoform 3 promotes the formation of filopodia by regulating the recruitment of actin-binding proteins to actin filaments.
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| Creed SJ, Desouza M, Bamburg JR, Gunning P, Stehn J.
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| Exp Cell Res 317(3):249-61. doi: 10.1016/j.yexcr.2010.10.019. Epub 2010 Oct 29.
2011
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| 13 | CFTD3, TPM3
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| Congenital fibre type disproportion associated with mutations in the tropomyosin 3 (TPM3) gene mimicking congenital myasthenia.
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| Munot P, Lashley D, Jungbluth H, Feng L, Pitt M, Robb SA, Palace J, Jayawant S, Kennet R, Beeson D, Cullup T, Abbs S, Laing N, Sewry C, Muntoni F.
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| Neuromuscul Disord 20(12):796-800. Epub 2010 Oct 14.
2010
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| 14 | TPM3
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| A cytoskeletal tropomyosin can compromise the structural integrity of skeletal muscle.
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| Kee AJ, Gunning PW, Hardeman EC.
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| Cell Motil Cytoskeleton 66(9):710-20. doi: 10.1002/cm.20400.
2009
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| 15 | NEM1, TPM3
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| Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin.
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| Lehtokari VL, Pelin K, Donner K, Voit T, Rudnik-Schöneborn S, Stoetter M, Talim B, Topaloglu H, Laing NG, Wallgren-Pettersson C.
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| Eur J Hum Genet 16(9):1055-61. Epub 2008 Apr 2.
2008
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| 16 | TPM1, TPM2, TPM3, TPM4
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| Human tropomyosin isoforms in the regulation of cytoskeleton functions.
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| Lin JJ, Eppinga RD, Warren KS, McCrae KR.
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| Adv Exp Med Biol 644:201-22. Review.
2008
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| 17 | TPM1, TPM2, TPM3, TPM4
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| Tropomyosins in skeletal muscle diseases.
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| Kee AJ, Hardeman EC.
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| Adv Exp Med Biol 644:143-57. Review.
2008
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| 18 | NEM1, TPM3
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| Mutations in TPM3 are a common cause of congenital fiber type disproportion.
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| Clarke NF, Kolski H, Dye DE, Lim E, Smith RL, Patel R, Fahey MC, Bellance R, Romero NB, Johnson ES, Labarre-Vila A, Monnier N, Laing NG, North KN.
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| Ann Neurol 63(3):329-37. 2008
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| 19 | TPM3, TTC9
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| Tetratricopeptide repeat domain 9A is an interacting protein for tropomyosin Tm5NM-1.
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| Cao S, Ho GH, Lin VC.
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| BMC Cancer 8:231. doi: 10.1186/1471-2407-8-231.
2008
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| 20 | ACOT2, AFAP1L1, ALG11, ANKS1A, ARMC6, ARPC1A, ARPC3, ARPC5L, ATG10, ATP5L, BAZ1A, BCAS2, C2orf44, CAPZA1, CAPZA2, CCDC47, CERS2, CMBL, CPSF2, CSTF3, CXorf56, EXT2, FAF2, FBXO4, FIBP, GLRX3, GPS1, GSKIP, INPP5K, KPNA4, KRT31, KRT32, KRT33A, KRT33B, KRT34, KRT36, LUC7L2, MAGED1, MED7, MMS22L, MPRIP, MPRIP, MRCL3, NAA25, NDN, NPEPPS, NRDE2, OLA1, ORCTL3, OSTF1, PH4B, PIP5K1B, PKIG, PMVK, PSMC1, PSMC2, PSPH, RAB11FIP1, RBX1, RNF219, RO60, RPS14, SF3B14, SF3B2, SFRS12, STK25, TLK2, TONSL, TPM3, TRMT112, TSPAN17, TWF2, UBE2M, UNC45A, UQCRC1, WRAP73, XPO7, ZRANB2
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| Large-scale mapping of human protein-protein interactions by mass spectrometry.
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| Ewing RM, Chu P, Elisma F, Li H, Taylor P, Climie S, McBroom-Cerajewski L, Robinson MD, O'Connor L, Li M, Taylor R, Dharsee M, Ho Y, Heilbut A, Moore L, Zhang S, Ornatsky O, Bukhman YV, Ethier M, Sheng Y, Vasilescu J, Abu-Farha M, Lambert JP, Duewel HS, Stewart II, Kuehl B, Hogue K, Colwill K, Gladwish K, Muskat B, Kinach R, Adams SL, Moran MF, Morin GB, Topaloglou T, Figeys D.
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| Mol Syst Biol 3:89. Epub 2007 Mar 13. 2007
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| 21 | NEM1, TPM3
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| A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: a clinical and pathological study.
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| Pénisson-Besnier I, Monnier N, Toutain A, Dubas F, Laing N.
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| Neuromuscul Disord 17(4):330-7. Epub 2007 Mar 21.
2007
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| 22 | PDGFRB, TPM3
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| TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia.
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| Rosati R, La Starza R, Luciano L, Gorello P, Matteucci C, Pierini V, Romoli S, Crescenzi B, Rotoli B, Martelli MF, Pane F, Mecucci C.
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| Leukemia 20(9):1623-4. Epub 2006 Jul 13. No abstract available.
2006
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| 23 | ALK, ATIC, CLTC, MSN, MYH9, RNF213, TFG, TPM3, TPM4
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| Non-muscle myosin heavy chain (MYH9): a new partner fused to ALK in anaplastic large cell lymphoma.
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| Lamant L, Gascoyne RD, Duplantier MM, Armstrong F, Raghab A, Chhanabhai M, Rajcan-Separovic E, Raghab J, Delsol G, Espinos E.
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| Genes Chromosomes Cancer 37(4):427-32. 2003
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| 24 | TPM3
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| Isolation and sequencing of a novel tropomyosin isoform preferentially associated with colon cancer.
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| Lin JL, Geng X, Bhattacharya SD, Yu JR, Reiter RS, Sastri B, Glazier KD, Mirza ZK, Wang KK, Amenta PS, Das KM, Lin JJ.
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| Gastroenterology 123(1):152-62. 2002
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| 25 | NEM1, TPM3
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| Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy.
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| Wattanasirichaigoon D, Swoboda KJ, Takada F, Tong HQ, Lip V, Iannaccone ST, Wallgren-Pettersson C, Laing NG, Beggs AH.
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| Neurology 59(4):613-7. 2002
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| 26 | NEM1, TPM3
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| A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy.
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| Corbett MA, Robinson CS, Dunglison GF, Yang N, Joya JE, Stewart AW, Schnell C, Gunning PW, North KN, Hardeman EC.
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| Hum Mol Genet 10(4):317-28. 2001
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| 27 | BLOM7, HAX1, MCKD1, SYT11, TPM3, UBAP2L
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| Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region.
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| Fuchshuber A, Kroiss S, Karle S, Berthold S, Huck K, Burton C, Rahman N, Koptides M, Deltas C, Otto E, Ruschendorf F, Feest T, Hildebrandt F.
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| Genomics 72(3):278-84. 2001
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| 28 | NEM1, TPM3
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| Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy.
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| Tan P, Briner J, Boltshauser E, Davis MR, Wilton SD, North K, Wallgren-Pettersson C, Laing NG.
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| Neuromuscul Disord 9(8):573-9. 1999
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| 29 | NTRK1, TPM3
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| A sequence analysis of the genomic regions involved in the rearrangements between TPM3 and NTRK1 genes producing TRK oncogenes in papillary thyroid carcinomas.
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| Butti MG, et al.
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| Genomics 28 : 15-24. 1995
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| 30 | TPM3, NEM1
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| Assignment of the human alpha-tropomyosin gene TPM3 to 1q22-q23 by fluorescence in situ hybridization.
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| Wilton SD, et al.
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| Cytogenet Cell Genet 68 : 122-124. 1995
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| 31 | NEM1, TPM3
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| A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy.
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| Laing NG, et al.
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| Nat Genet 9 : 75-79. 1995
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| 32 | TPM3
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| TaqI RFLP of the human tropomyosin gene (TPM3) involved in the generation of the TRK oncogene.
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| Michieli P, et al.
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| Nucleic Acids Res 19 : 4796. 1991
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| 33 | TPM3
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| The human tropomyosin gene involved in the generation of the TRK oncogene maps to chromosome 1q31.
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| Radice P, et al.
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| Oncogene 6 : 2145-2148. 1991
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