Alaşehirli B - Search Results

1

Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome.

Gürsoy S, Erdal E, Herken H, Madenci E, Alaşehirli B, Erdal N. Gürsoy S, et al. Among authors: alasehirli b. Rheumatol Int. 2003 May;23(3):104-7. doi: 10.1007/s00296-002-0260-5. Epub 2002 Oct 22. Rheumatol Int. 2003. PMID: 12739038

2

CYP gene expressions in obesity-associated metabolic syndrome.

Tabur S, Oztuzcu S, Oguz E, Demiryürek S, Dagli H, Alasehirli B, Ozkaya M, Demiryürek AT. Tabur S, et al. Among authors: alasehirli b. Obes Res Clin Pract. 2016 Nov-Dec;10(6):719-723. doi: 10.1016/j.orcp.2016.03.001. Epub 2016 Mar 22. Obes Res Clin Pract. 2016. PMID: 27010496

3

Investigation of intercellular adhesion molecules (ICAMs) gene expressions in patients with Barrett's esophagus.

Alasehirli B, Oğuz E, Oksuzler E, Koruk I, Oztuzcu S, Ozkara E, Karakok M, Erbagcı AB, Demiryurek AT. Alasehirli B, et al. Tumour Biol. 2014 May;35(5):4907-12. doi: 10.1007/s13277-014-1644-3. Epub 2014 Jan 29. Tumour Biol. 2014. PMID: 24474251

4

Investigation of the esophageal Rho-kinase expression in patients with Barrett's esophagus.

Demiryürek S, Koruk I, Bozdag Z, Ozkara E, Kaplan DS, Oztuzcu S, Cetinkaya A, Alasehirli B, Demiryürek AT. Demiryürek S, et al. Among authors: alasehirli b. Ultrastruct Pathol. 2013 Aug;37(4):284-9. doi: 10.3109/01913123.2013.797064. Epub 2013 Jun 21. Ultrastruct Pathol. 2013. PMID: 23789633

5

Association between Rho-kinase (ROCK2) gene polymorphisms and Behçet's disease.

Oguz E, Alasehirli B, Pehlivan Y, Onat AM, Oztuzcu S, Ozkara E, Kisacik B, Camci C, Demiryürek AT. Oguz E, et al. Among authors: alasehirli b. Transl Res. 2012 Dec;160(6):428-34. doi: 10.1016/j.trsl.2012.08.002. Epub 2012 Aug 30. Transl Res. 2012. PMID: 22939913

6

Lack of association between the C276T polymorphism of the neuronal nitric oxide synthase gene and migraine.

Alaşehirli B, Akçalı A, Demiryürek AT, Özel A, Erdal ME, Neyal M. Alaşehirli B, et al. Int J Neurosci. 2013 Jan;123(1):50-4. doi: 10.3109/00207454.2012.724743. Epub 2012 Oct 3. Int J Neurosci. 2013. PMID: 22937753

7

DD genotype of ACE gene in boys: may it be a risk factor for minimal change nephrotic syndrome?

Alasehirli B, Balat A, Büyükçelik M. Alasehirli B, et al. Ren Fail. 2012;34(1):19-23. doi: 10.3109/0886022X.2011.623493. Epub 2011 Oct 21. Ren Fail. 2012. PMID: 22017506

8

Lack of association between the Thr431Asn and Arg83Lys polymorphisms of the ROCK2 gene and diabetic retinopathy.

Demiryurek AT, Erbagci I, Oztuzcu S, Alasehirli B, Ozkara E, Seker M, Sönmez A, Ozsan M, Camci C. Demiryurek AT, et al. Among authors: alasehirli b. Curr Eye Res. 2010 Dec;35(12):1128-34. doi: 10.3109/02713683.2010.507903. Epub 2010 Oct 20. Curr Eye Res. 2010. PMID: 20961215

9

Nitric oxide synthase gene polymorphisms in children with minimal change nephrotic syndrome.

Alasehirli B, Balat A, Barlas O, Kont A. Alasehirli B, et al. Pediatr Int. 2009 Feb;51(1):75-8. doi: 10.1111/j.1442-200X.2008.02655.x. Pediatr Int. 2009. PMID: 19371282

10

Which genotype of MAO gene that the patients have are likely to be most susceptible to the symptoms of fibromyalgia?

Gürsoy S, Erdal E, Sezgin M, Barlas IO, Aydeniz A, Alaşehirli B, Sahin G. Gürsoy S, et al. Among authors: alasehirli b. Rheumatol Int. 2008 Feb;28(4):307-11. doi: 10.1007/s00296-007-0454-y. Epub 2007 Sep 20. Rheumatol Int. 2008. PMID: 17885758

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