PubMed for id: 8557

Year	Number of Results
1993	3
1997	2
1998	3
2000	3
2001	3
2002	6
2003	2
2004	5
2005	4
2006	11
2007	3
2008	6
2009	4
2010	4
2011	5
2012	1
2013	3
2014	3
2015	2
2016	1
2017	2
2018	1
2019	1
2020	6
2021	3
2022	1
2023	2
2024	0

1

TCAP gene is not a common cause of cardiomyopathy in Iranian patients.

Alaei Z, Zamani N, Rabbani B, Mahdieh N. Alaei Z, et al. Eur J Med Res. 2023 Sep 26;28(1):376. doi: 10.1186/s40001-023-01019-4. Eur J Med Res. 2023. PMID: 37752589 Free PMC article.

2

The clinical features and TCAP mutation spectrum in a Chinese cohort of patients with limb-girdle muscular dystrophy R7.

Lv X, Lin F, Wu W, Wang H, Luo Y, Wang Z, Yan C, Lv H, Luo S, Lin P. Lv X, et al. Hum Mol Genet. 2023 Jul 20;32(15):2502-2510. doi: 10.1093/hmg/ddad090. Hum Mol Genet. 2023. PMID: 37216648

3

Distal myopathy due to TCAP variants in four unrelated Chinese patients.

Lv X, Gao F, Dai T, Zhao D, Jiang W, Geng H, Liu F, Lin P, Yan C. Lv X, et al. Neurogenetics. 2021 Mar;22(1):1-10. doi: 10.1007/s10048-020-00623-4. Epub 2020 Aug 6. Neurogenetics. 2021. PMID: 32761539

4

Telethonin variants found in Brugada syndrome, J-wave pattern ECG, and ARVC reduce peak Na_v 1.5 currents in HEK-293 cells.

Turker I, Makiyama T, Ueyama T, Shimizu A, Yamakawa M, Chen PS, Vatta M, Horie M, Ai T. Turker I, et al. Pacing Clin Electrophysiol. 2020 Aug;43(8):838-846. doi: 10.1111/pace.13996. Epub 2020 Jul 7. Pacing Clin Electrophysiol. 2020. PMID: 32588437

5

Identification of a novel titin-cap/telethonin mutation in a Portuguese family with hypertrophic cardiomyopathy.

Toste A, Perrot A, Özcelik C, Cardim N. Toste A, et al. Rev Port Cardiol (Engl Ed). 2020 Jun;39(6):317-327. doi: 10.1016/j.repc.2019.12.007. Epub 2020 Jun 18. Rev Port Cardiol (Engl Ed). 2020. PMID: 32565061 Free article. English, Portuguese.

6

Limb girdle muscular dystrophy 2G in a religious minority of Bulgarian Muslims homozygous for the c.75G>A, p.Trp25X mutation.

Chamova T, Bichev S, Todorov T, Gospodinova M, Taneva A, Kastreva K, Zlatareva D, Krupev M, Hadjiivanov R, Guergueltcheva V, Grozdanova L, Tzoneva D, Huebner A, V der Hagen M, Schoser B, Lochmüller H, Todorova A, Tournev I. Chamova T, et al. Neuromuscul Disord. 2018 Aug;28(8):625-632. doi: 10.1016/j.nmd.2018.05.005. Epub 2018 May 17. Neuromuscul Disord. 2018. PMID: 29935994

7

Expression and purification of a difficult sarcomeric protein: Telethonin.

Tan H, Su W, Wang P, Zhang W, Sattler M, Zou P. Tan H, et al. Protein Expr Purif. 2017 Dec;140:74-80. doi: 10.1016/j.pep.2017.08.007. Epub 2017 Aug 12. Protein Expr Purif. 2017. PMID: 28811266

8

Novel TCAP mutation c.32C>A causing limb girdle muscular dystrophy 2G.

Francis A, Sunitha B, Vinodh K, Polavarapu K, Katkam SK, Modi S, Bharath MM, Gayathri N, Nalini A, Thangaraj K. Francis A, et al. PLoS One. 2014 Jul 23;9(7):e102763. doi: 10.1371/journal.pone.0102763. eCollection 2014. PLoS One. 2014. PMID: 25055047 Free PMC article.

9

Deletion of Glu at codon 13 of the TCAP gene encoding the titin-cap-telethonin is a rare polymorphism in a large Italian population.

Marziliano N, Pilotto A, Grasso M, Pasotti M, Arbustini E. Marziliano N, et al. Mol Genet Metab. 2006 Nov;89(3):286-7. doi: 10.1016/j.ymgme.2006.03.012. Epub 2006 May 2. Mol Genet Metab. 2006. PMID: 16650785 No abstract available.

10

Deletion of Glu at codon 13 in the TCAP gene encoding the Z-disc protein titin-cap/telethonin is a rare non-synonymous polymorphism.

Perrot A, Posch MG, Osterziel KJ. Perrot A, et al. Mol Genet Metab. 2006 Jun;88(2):199-200. doi: 10.1016/j.ymgme.2006.01.004. Epub 2006 Feb 21. Mol Genet Metab. 2006. PMID: 16490376 No abstract available.

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