Sinici I - Search Results

1

In cellulo examination of a beta-alpha hybrid construct of beta-hexosaminidase A subunits, reported to interact with the GM2 activator protein and hydrolyze GM2 ganglioside.

Sinici I, Yonekawa S, Tkachyova I, Gray SJ, Samulski RJ, Wakarchuk W, Mark BL, Mahuran DJ. Sinici I, et al. PLoS One. 2013;8(3):e57908. doi: 10.1371/journal.pone.0057908. Epub 2013 Mar 4. PLoS One. 2013. PMID: 23483939 Free PMC article.

2

Assessing the severity of the small inframe deletion mutation in the alpha-subunit of beta-hexosaminidase A found in the Turkish population by reproducing it in the more stable beta-subunit.

Sinici I, Tropak MB, Mahuran DJ, Ozkara HA. Sinici I, et al. J Inherit Metab Dis. 2004;27(6):747-56. doi: 10.1023/B:BOLI.0000045759.12935.76. J Inherit Metab Dis. 2004. PMID: 15505380 Free PMC article.

3

Comparison of HCMV IE and EF-1 promoters for the stable expression of beta-subunit of hexosaminidase in CHO cell lines.

Sinici I, Zarghooni M, Tropak MB, Mahuran DJ, Ozkara HA. Sinici I, et al. Biochem Genet. 2006 Apr;44(3-4):173-80. doi: 10.1007/s10528-006-9016-3. Epub 2006 Apr 28. Biochem Genet. 2006. PMID: 16645900 Free PMC article. No abstract available.

4

Biochemical and molecular characterization of mutant hexosaminidase A in a Turkish family.

Sinici I, Ozkara HA, Topçu M, Ciliv G. Sinici I, et al. Pediatr Int. 2003 Feb;45(1):16-22. doi: 10.1046/j.1442-200x.2003.01669.x. Pediatr Int. 2003. PMID: 12654063

5

Identification of two novel arylsulfatase A mutations with a polymorphism as a cause of metachromatic leukodystrophy.

Onder E, Sinici I, Müjgan Sönmez F, Topçu M, Ozkara HA. Onder E, et al. Among authors: sinici i. Neurol Res. 2009 Feb;31(1):60-6. doi: 10.1179/016164108X323762. Epub 2008 Sep 3. Neurol Res. 2009. PMID: 18768108

6

Identification of 7th hexosaminidase A mutation of Tay-Sachs disease in the Turkish population.

Sinici I, Onder E, Topçu M, Ozkara HA. Sinici I, et al. Turk J Pediatr. 2007 Jul-Sep;49(3):337-8. Turk J Pediatr. 2007. PMID: 17990595 No abstract available.

7

Protective role of 27bp repeat polymorphism in intron 4 of eNOS gene in lacunar infarction.

Yemişçi M, Sinici I, Ozkara HA, Hayran M, Ay H, Celtikçi B, Onder E, Büyükşerbetci G, Kaya EB, Tokgözoglu L, Dalkara T. Yemişçi M, et al. Among authors: sinici i. Free Radic Res. 2009 Mar;43(3):272-9. doi: 10.1080/10715760802691489. Epub 2009 Jan 31. Free Radic Res. 2009. PMID: 19184759

8

Why are they having infant colic? A nested case-control study.

Yalçin SS, Orün E, Mutlu B, Madendağ Y, Sinici I, Dursun A, Ozkara HA, Ustünyurt Z, Kutluk S, Yurdakök K. Yalçin SS, et al. Among authors: sinici i. Paediatr Perinat Epidemiol. 2010 Nov;24(6):584-96. doi: 10.1111/j.1365-3016.2010.01150.x. Epub 2010 Aug 17. Paediatr Perinat Epidemiol. 2010. PMID: 20955236

9

Distribution of endothelial nitric oxide synthase gene polymorphisms in Turkish population.

Sinici I, Karahan S, Atalar E. Sinici I, et al. J Investig Med. 2009 Oct;57(7):769-76. doi: 10.2310/JIM.0b013e3181b91bbd. J Investig Med. 2009. PMID: 19730129

10

T-786C polymorphism in promoter of eNOS gene as genetic risk factor in patients with erectile dysfunction in Turkish population.

Sinici I, Güven EO, Serefoğlu E, Hayran M. Sinici I, et al. Urology. 2010 Apr;75(4):955-60. doi: 10.1016/j.urology.2009.06.063. Epub 2009 Oct 2. Urology. 2010. PMID: 19800665

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