Sibin MK - Search Results

1

Germline PMS2 and somatic POLE exonuclease mutations cause hypermutability of the leading DNA strand in biallelic mismatch repair deficiency syndrome brain tumours.

Andrianova MA, Chetan GK, Sibin MK, Mckee T, Merkler D, Narasinga RK, Ribaux P, Blouin JL, Makrythanasis P, Seplyarskiy VB, Antonarakis SE, Nikolaev SI. Andrianova MA, et al. Among authors: sibin mk. J Pathol. 2017 Nov;243(3):331-341. doi: 10.1002/path.4957. Epub 2017 Sep 28. J Pathol. 2017. PMID: 28805995

2

CDKN2A exon-wise deletion status and novel somatic mutations in Indian glioma patients.

Sibin MK, Bhat DI, Lavanya Ch, Manoj MJ, Aakershita S, Chetan GK. Sibin MK, et al. Tumour Biol. 2014 Feb;35(2):1467-72. doi: 10.1007/s13277-013-1201-5. Epub 2013 Sep 25. Tumour Biol. 2014. PMID: 24065197

3

CDKN2A (p16) mRNA decreased expression is a marker of poor prognosis in malignant high-grade glioma.

Sibin MK, Bhat DI, Narasingarao KV, Lavanya Ch, Chetan GK. Sibin MK, et al. Tumour Biol. 2015 Sep;36(10):7607-14. doi: 10.1007/s13277-015-3480-5. Epub 2015 Apr 29. Tumour Biol. 2015. PMID: 25921285

4

Effect of rs11614913 Polymorphism on Mature miR196a2 Expression and its Target Gene HOXC8 Expression in Human Glioma.

Sibin MK, Harshitha SM, Narasingarao KV, Dhananjaya IB, Dhaval PS, Chetan GK. Sibin MK, et al. J Mol Neurosci. 2017 Feb;61(2):144-151. doi: 10.1007/s12031-016-0855-z. Epub 2016 Oct 28. J Mol Neurosci. 2017. PMID: 27796868

5

Factor XIII polymorphism and risk of aneurysmal subarachnoid haemorrhage in a south Indian population.

Suvatha A, Sibin MK, Bhat DI, Narasingarao KVL, Vazhayil V, Chetan GK. Suvatha A, et al. Among authors: sibin mk. BMC Med Genet. 2018 Sep 5;19(1):159. doi: 10.1186/s12881-018-0674-x. BMC Med Genet. 2018. PMID: 30185149 Free PMC article.

6

CD133 and BMI1 expressions and its prognostic role in primary glioblastoma.

Sibin MK, Lavanya CH, Bhat DI, Rao N, Geethashree N, Vibhuti W, Chetan GK. Sibin MK, et al. J Genet. 2015 Dec;94(4):689-96. doi: 10.1007/s12041-015-0583-0. J Genet. 2015. PMID: 26690524 Free article.

7

Polymorphisms of apolipoprotein E and aneurysmal subarachnoid haemorrhage: A meta-analysis.

Arati S, Sibin MK, Bhat DI, Narasingarao KV, Chetan GK. Arati S, et al. Among authors: sibin mk. Meta Gene. 2016 Jun 17;9:151-8. doi: 10.1016/j.mgene.2016.06.003. eCollection 2016 Sep. Meta Gene. 2016. PMID: 27408823 Free PMC article. Review.

8

Down regulation of human telomerase reverse transcriptase (hTERT) expression by BIBR1532 in human glioblastoma LN18 cells.

Lavanya C, Venkataswamy MM, Sibin MK, Srinivas Bharath MM, Chetan GK. Lavanya C, et al. Among authors: sibin mk. Cytotechnology. 2018 Aug;70(4):1143-1154. doi: 10.1007/s10616-018-0205-9. Epub 2018 Mar 15. Cytotechnology. 2018. PMID: 29546682 Free PMC article.

9

Two gene polymorphisms (rs4977756 and rs11515) in CDKN2A/B and glioma risk in South Indian population.

Sibin MK, Dhananjaya IB, Narasingarao KV, Harshitha SM, Jeru-Manoj M, Chetan GK. Sibin MK, et al. Meta Gene. 2016 Jul 17;9:215-8. doi: 10.1016/j.mgene.2016.07.010. eCollection 2016 Sep. Meta Gene. 2016. PMID: 27617221 Free PMC article.

10

Role of APOE and IL18RAP gene polymorphisms in cervical spondylotic myelopathy in Indian population.

Diptiranjan S, Harshitha SM, Sibin MK, Arati S, Chetan GK, Bhat DI. Diptiranjan S, et al. Among authors: sibin mk. J Clin Neurosci. 2019 Aug;66:83-86. doi: 10.1016/j.jocn.2019.05.017. Epub 2019 May 21. J Clin Neurosci. 2019. PMID: 31126849

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