Sezerman U - Search Results

1

A possible founder mutation in FZD6 gene in a Turkish family with autosomal recessive nail dysplasia.

Saygı C, Alanay Y, Sezerman U, Yenenler A, Özören N. Saygı C, et al. Among authors: sezerman u. BMC Med Genet. 2019 Jan 14;20(1):15. doi: 10.1186/s12881-019-0746-6. BMC Med Genet. 2019. PMID: 30642273 Free PMC article.

2

Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case report.

Bozkurt T, Alanay Y, Isik U, Sezerman U. Bozkurt T, et al. Among authors: sezerman u. BMC Med Genomics. 2021 Jul 31;14(1):197. doi: 10.1186/s12920-021-01045-3. BMC Med Genomics. 2021. PMID: 34332575 Free PMC article.

3

Predicting the impact of mutations on the specific activity of Bacillus thermocatenulatus lipase using a combined approach of docking and molecular dynamics.

Yukselen O, Timucin E, Sezerman U. Yukselen O, et al. Among authors: sezerman u. J Mol Recognit. 2016 Oct;29(10):466-75. doi: 10.1002/jmr.2545. Epub 2016 Apr 14. J Mol Recognit. 2016. PMID: 27074770

4

Clustering of protein families into functional subtypes using Relative Complexity Measure with reduced amino acid alphabets.

Albayrak A, Otu HH, Sezerman UO. Albayrak A, et al. BMC Bioinformatics. 2010 Aug 18;11:428. doi: 10.1186/1471-2105-11-428. BMC Bioinformatics. 2010. PMID: 20718947 Free PMC article.

5

Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation.

Everest E, Ahangari M, Uygunoglu U, Tutuncu M, Bulbul A, Saip S, Duman T, Sezerman U, Reich DS, Riley BP, Siva A, Tahir Turanli E. Everest E, et al. Among authors: sezerman u. Sci Rep. 2022 Oct 10;12(1):16984. doi: 10.1038/s41598-022-21484-x. Sci Rep. 2022. PMID: 36216875 Free PMC article.

6

RDDSVM: accurate prediction of A-to-I RNA editing sites from sequence using support vector machines.

Tac HA, Koroglu M, Sezerman U. Tac HA, et al. Among authors: sezerman u. Funct Integr Genomics. 2021 Nov;21(5-6):633-643. doi: 10.1007/s10142-021-00805-9. Epub 2021 Sep 16. Funct Integr Genomics. 2021. PMID: 34529170

7

Investigation of base excision repair gene variants in late-onset Alzheimer's disease.

Ertuzun T, Semerci A, Cakir ME, Ekmekcioglu A, Gok MO, Soltys DT, de Souza-Pinto NC, Sezerman U, Muftuoglu M. Ertuzun T, et al. Among authors: sezerman u. PLoS One. 2019 Aug 15;14(8):e0221362. doi: 10.1371/journal.pone.0221362. eCollection 2019. PLoS One. 2019. PMID: 31415677 Free PMC article. Clinical Trial.

8

Lipase and Water in a Deep Eutectic Solvent: Molecular Dynamics and Experimental Studies of the Effects of Water-In-Deep Eutectic Solvents on Lipase Stability.

Shehata M, Unlu A, Sezerman U, Timucin E. Shehata M, et al. Among authors: sezerman u. J Phys Chem B. 2020 Oct 8;124(40):8801-8810. doi: 10.1021/acs.jpcb.0c07041. Epub 2020 Sep 28. J Phys Chem B. 2020. PMID: 32940465

9

Differential gene expression analysis of human cumulus cells.

Demiray SB, Goker ENT, Tavmergen E, Yilmaz O, Calimlioglu N, Soykam HO, Oktem G, Sezerman U. Demiray SB, et al. Among authors: sezerman u. Clin Exp Reprod Med. 2019 Jun;46(2):76-86. doi: 10.5653/cerm.2019.46.2.76. Epub 2019 Jun 1. Clin Exp Reprod Med. 2019. PMID: 31181875 Free PMC article.

10

Analysis of the interplay between methylation and expression reveals its potential role in cancer aetiology.

Ozer B, Sezerman U. Ozer B, et al. Among authors: sezerman u. Funct Integr Genomics. 2017 Jan;17(1):53-68. doi: 10.1007/s10142-016-0533-9. Epub 2016 Nov 7. Funct Integr Genomics. 2017. PMID: 27819121

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