PubMed (GeneRIF) for id: 343641

Year	Number of Results
2008	1
2010	2
2011	2
2012	3
2013	4
2014	3
2015	1
2017	2
2018	2
2019	1
2020	1
2021	1
2024	0

1

TGM6 might not be a specific causative gene for spinocerebellar ataxia resulting from genetic analysis and functional study.

Cheng HL, Dong HL, Liu DS, Ni W, Ma Y, Yang L, Du YC, Chen DF, Dong Y, Wu ZY. Cheng HL, et al. Gene. 2021 May 5;779:145495. doi: 10.1016/j.gene.2021.145495. Epub 2021 Feb 13. Gene. 2021. PMID: 33588035

2

TGM6 variants in Parkinson's disease: clinical findings and functional evidence.

Chen K, Lu Y, Peng F, Yu HL, Wu JY, Tan Y, Zhao YX. Chen K, et al. J Integr Neurosci. 2020 Mar 30;19(1):51-64. doi: 10.31083/j.jin.2020.01.1203. J Integr Neurosci. 2020. PMID: 32259886 Free article.

3

A significant inflation in TGM6 genetic risk casts doubt in its causation in spinocerebellar ataxia type 35.

Fung JLF, Tsang MHY, Leung GKC, Yeung KS, Mak CCY, Fung CW, Chan SHS, Yu MHC, Chung BHY. Fung JLF, et al. Parkinsonism Relat Disord. 2019 Jun;63:42-45. doi: 10.1016/j.parkreldis.2019.01.013. Epub 2019 Jan 17. Parkinsonism Relat Disord. 2019. PMID: 30670339

4

Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese.

Zheng R, Li Z, He F, Liu H, Chen J, Chen J, Xie X, Zhou J, Chen H, Wu X, Wu J, Chen B, Liu Y, Cui H, Fan L, Sha W, Liu Y, Wang J, Huang X, Zhang L, Xu F, Wang J, Feng Y, Qin L, Yang H, Liu Z, Cui Z, Liu F, Chen X, Gao S, Sun S, Shi Y, Ge B. Zheng R, et al. Nat Commun. 2018 Oct 4;9(1):4072. doi: 10.1038/s41467-018-06539-w. Nat Commun. 2018. PMID: 30287856 Free PMC article.

5

Mutations in TGM6 induce the unfolded protein response in SCA35.

Tripathy D, Vignoli B, Ramesh N, Polanco MJ, Coutelier M, Stephen CD, Canossa M, Monin ML, Aeschlimann P, Turberville S, Aeschlimann D, Schmahmann JD, Hadjivassiliou M, Durr A, Pandey UB, Pennuto M, Basso M. Tripathy D, et al. Hum Mol Genet. 2017 Oct 1;26(19):3749-3762. doi: 10.1093/hmg/ddx259. Hum Mol Genet. 2017. PMID: 28934387

6

TGM6 gene mutations in undiagnosed cerebellar ataxia patients.

Yang ZH, Shi MM, Liu YT, Wang YL, Luo HY, Wang ZL, Shi CH, Xu YM. Yang ZH, et al. Parkinsonism Relat Disord. 2018 Jan;46:84-86. doi: 10.1016/j.parkreldis.2017.07.001. Epub 2017 Jul 4. Parkinsonism Relat Disord. 2018. PMID: 28927799 No abstract available.

7

Spinocerebellar ataxia 35: novel mutations in TGM6 with clinical and genetic characterization.

Guo YC, Lin JJ, Liao YC, Tsai PC, Lee YC, Soong BW. Guo YC, et al. Neurology. 2014 Oct 21;83(17):1554-61. doi: 10.1212/WNL.0000000000000909. Epub 2014 Sep 24. Neurology. 2014. PMID: 25253745

8

Positional cloning and next-generation sequencing identified a TGM6 mutation in a large Chinese pedigree with acute myeloid leukaemia.

Pan LL, Huang YM, Wang M, Zhuang XE, Luo DF, Guo SC, Zhang ZS, Huang Q, Lin SL, Wang SY. Pan LL, et al. Eur J Hum Genet. 2015 Feb;23(2):218-23. doi: 10.1038/ejhg.2014.67. Epub 2014 Apr 23. Eur J Hum Genet. 2015. PMID: 24755948 Free PMC article.

9

Genetics of dizziness: cerebellar and vestibular disorders.

Requena T, Espinosa-Sanchez JM, Lopez-Escamez JA. Requena T, et al. Curr Opin Neurol. 2014 Feb;27(1):98-104. doi: 10.1097/WCO.0000000000000053. Curr Opin Neurol. 2014. PMID: 24275721 Review.

10

Transglutaminase 6 interacts with polyQ proteins and promotes the formation of polyQ aggregates.

Guan WJ, Xia KD, Ma YT, Liu YT, Shi YT, Jiang H, Shen L, Xia K, Li JD, Tang BS, Wang JL. Guan WJ, et al. Biochem Biophys Res Commun. 2013 Jul 19;437(1):94-100. doi: 10.1016/j.bbrc.2013.06.044. Epub 2013 Jun 22. Biochem Biophys Res Commun. 2013. PMID: 23800413

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

19 results

Results by year