Kan D - Search Results

1

MEFV gene mutations and its impact on the clinical course in ulcerative colitis patients.

Yıldırım B, Tuncer C, Kan D, Tunc B, Demirag MD, Ferda Percın E, Haznedaroglu S, Alagozlu H. Yıldırım B, et al. Among authors: kan d. Rheumatol Int. 2011 Jul;31(7):859-64. doi: 10.1007/s00296-010-1380-y. Epub 2010 Mar 12. Rheumatol Int. 2011. PMID: 20224922

2

ABCB1 C3435T polymorphism is associated with susceptibility to major depression, but not with a clinical response to citalopram in a Turkish population.

Ozbey G, Yucel B, Taycan SE, Kan D, Bodur NE, Arslan T, Percin F, Yuksel N, Guzey C, Uluoglu C. Ozbey G, et al. Among authors: kan d. Pharmacol Rep. 2014 Apr;66(2):235-8. doi: 10.1016/j.pharep.2013.09.004. Epub 2014 Mar 2. Pharmacol Rep. 2014. PMID: 24911075

3

Influence of ABCB1 polymorphisms and serum concentrations on venlafaxine response in patients with major depressive disorder.

Ozbey G, Celikel FC, Cumurcu BE, Kan D, Yucel B, Hasbek E, Percin F, Guzey IC, Uluoglu C. Ozbey G, et al. Among authors: kan d. Nord J Psychiatry. 2017 Apr;71(3):230-237. doi: 10.1080/08039488.2016.1268203. Epub 2017 Jan 12. Nord J Psychiatry. 2017. PMID: 28079463

4

A case with a ring chromosome 22.

Koç A, Karaer K, Ergün MA, Yirmibeş-Karaoğuz M, Kan D, Cansu A, Perçin F. Koç A, et al. Among authors: kan d. Turk J Pediatr. 2008 Mar-Apr;50(2):193-6. Turk J Pediatr. 2008. PMID: 18664089

5

Lack of association between matrix metalloproteinase-9 and endothelial nitric oxide synthase gene polymorphisms and coronary artery disease in Turkish population.

Alp E, Menevse S, Tulmac M, Kan D, Yalcin R, Erkan AF, Cengel A. Alp E, et al. Among authors: kan d. DNA Cell Biol. 2009 Jul;28(7):343-50. doi: 10.1089/dna.2009.0866. DNA Cell Biol. 2009. PMID: 19435423

6

A boy with small supernumerary marker chromosome X identified by FISH.

Koç A, Yirmibeş Karaoğuz M, Pala E, Kan D, Karaer K, Gücüyener K, Perçin EF. Koç A, et al. Among authors: kan d. Genet Couns. 2007;18(4):393-9. Genet Couns. 2007. PMID: 18286820

7

Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.

Ergun MA, Balci S, Konaç E, Kan D, Menevşe S, Bartsch O. Ergun MA, et al. Among authors: kan d. Turk J Pediatr. 2004 Oct-Dec;46(4):384-7. Turk J Pediatr. 2004. PMID: 15641279

8

An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.

Koç A, Kan D, Karaer K, Ergün MA, Karaoğuz MY, Gücüyener K, Hinreiner S, Liehr T, Perçin EF. Koç A, et al. Among authors: kan d. Eur J Pediatr. 2008 Jun;167(6):655-9. doi: 10.1007/s00431-007-0568-y. Epub 2007 Aug 1. Eur J Pediatr. 2008. PMID: 17668239

9

Transposition of great arteries in an infant born after prenatal diagnosis of trisomy 20 mosaicism.

Karaoguz MY, Pala E, Kula S, Karaer K, Kan D, Nas T, Tunaoglu S. Karaoguz MY, et al. Among authors: kan d. Genet Couns. 2007;18(4):437-43. Genet Couns. 2007. PMID: 18286825

10

Effect of ionizing radiation on the pteridine metabolic pathway and evaluation of its cytotoxicity in exposed hospital staff.

Engin AB, Ergun MA, Yurtcu E, Kan D, Sahin G. Engin AB, et al. Among authors: kan d. Mutat Res. 2005 Aug 1;585(1-2):184-92. doi: 10.1016/j.mrgentox.2005.05.005. Mutat Res. 2005. PMID: 15998597

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