Cine N - Search Results

1

Autosomal recessive idiopathic epilepsy in an inbred family from Turkey: identification of a putative locus on chromosome 9q32-33.

Baykan B, Madia F, Bebek N, Gianotti S, Güney AI, Cine N, Bianchi A, Gökyiğit A, Zara F. Baykan B, et al. Among authors: cine n. Epilepsia. 2004 May;45(5):479-87. doi: 10.1111/j.0013-9580.2004.30903.x. Epilepsia. 2004. PMID: 15101829 Free article.

2

Association of MDR1 (C3435T) polymorphism and resistance to carbamazepine in epileptic patients from Turkey.

Ozgon GO, Bebek N, Gul G, Cine N. Ozgon GO, et al. Among authors: cine n. Eur Neurol. 2008;59(1-2):67-70. doi: 10.1159/000109264. Epub 2007 Oct 4. Eur Neurol. 2008. PMID: 17917461 Clinical Trial.

3

Expression analysis and clinical correlation of aquaporin 1 and 4 genes in human hippocampal sclerosis.

Bebek N, Özdemir Ö, Sayitoglu M, Hatırnaz O, Baykan B, Gürses C, Sencer A, Karasu A, Tüzün E, Üzün I, Akat S, Cine N, Sargin Kurt G, Imer M, Ozbek U, Canbolat A, Gökyigit A. Bebek N, et al. Among authors: cine n. J Clin Neurosci. 2013 Nov;20(11):1564-70. doi: 10.1016/j.jocn.2012.12.023. Epub 2013 Aug 6. J Clin Neurosci. 2013. PMID: 23928039

4

Unbalanced 3;22 translocation with 22q11 and 3p deletion syndrome.

Dundar M, Kiraz A, Tasdemir S, Akalin H, Kurtoglu S, Hafo F, Cine N, Savli H. Dundar M, et al. Among authors: cine n. Am J Med Genet A. 2010 Nov;152A(11):2791-5. doi: 10.1002/ajmg.a.33249. Am J Med Genet A. 2010. PMID: 20949503

5

HLA-DQ alleles in patients with celiac disease in Turkey.

Tüysüz B, Dursun A, Kutlu T, Sökücü S, Cine N, Süoğlu O, Erkan T, Erginel-Unaltuna N, Tümay G. Tüysüz B, et al. Among authors: cine n. Tissue Antigens. 2001 Jun;57(6):540-2. doi: 10.1034/j.1399-0039.2001.057006540.x. Tissue Antigens. 2001. PMID: 11556984

6

I405V and TaqIB polymorphisms of the cholesteryl ester transfer protein and their relation to serum lipid and lipoprotein levels in a Turkish population.

Doğru-Abbasoğlu S, Parildar-Karpuzoğlu H, Depboylu B, Cine N, Uysal M, Aykaç-Toker G. Doğru-Abbasoğlu S, et al. Among authors: cine n. Cell Biochem Funct. 2009 Mar;27(2):76-80. doi: 10.1002/cbf.1536. Cell Biochem Funct. 2009. PMID: 19165812

7

Two four-marker haplotypes on 7q36.1 region indicate that the potassium channel gene HERG1 (KCNH2, Kv11.1) is related to schizophrenia: a case control study.

Atalar F, Acuner TT, Cine N, Oncu F, Yesilbursa D, Ozbek U, Turkcan S. Atalar F, et al. Among authors: cine n. Behav Brain Funct. 2010 May 28;6:27. doi: 10.1186/1744-9081-6-27. Behav Brain Funct. 2010. PMID: 20507645 Free PMC article.

8

A case of del(13)(q14.2)(q31.3) associated with hypothyroidism, hypertriglyceridemia, hypercholesterolemia and total ophthalmoplegia.

Malbora B, Meral C, Malbora N, Sunnetci D, Cine N, Savli H. Malbora B, et al. Among authors: cine n. Gene. 2012 May 1;498(2):296-9. doi: 10.1016/j.gene.2012.02.002. Epub 2012 Feb 22. Gene. 2012. PMID: 22387206

9

The effect of angiotensin converting enzyme gene polymorphism on chronic allograft dysfunction in living donor renal transplant recipients.

Yildiz A, Yazici H, Cine N, Akkaya V, Kayacan SM, Sever MS, Erginel-Unaltuna N. Yildiz A, et al. Among authors: cine n. Clin Transplant. 2002 Jun;16(3):173-9. doi: 10.1034/j.1399-0012.2002.01058.x. Clin Transplant. 2002. PMID: 12010139

10

Association of a polymorphism of the ecNOS gene with myocardial infarction in a subgroup of Turkish MI patients.

Cine N, Hatemi AC, Erginel-Unaltuna N. Cine N, et al. Clin Genet. 2002 Jan;61(1):66-70. doi: 10.1034/j.1399-0004.2002.610113.x. Clin Genet. 2002. PMID: 11903359

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