Ozkul Y - Search Results

1

The molecular basis and genotype-phenotype correlations of congenital adrenal hyperplasia (CAH) in Anatolian population.

Dundar A, Bayramov R, Onal MG, Akkus M, Dogan ME, Kenanoglu S, Cerrah Gunes M, Kazimli U, Ozbek MN, Ercan O, Yildirim R, Celmeli G, Parlak M, Dundar I, Hatipoglu N, Unluhizarci K, Akalin H, Ozkul Y, Saatci C, Dundar M. Dundar A, et al. Among authors: ozkul y. Mol Biol Rep. 2019 Aug;46(4):3677-3690. doi: 10.1007/s11033-019-04809-4. Epub 2019 Apr 20. Mol Biol Rep. 2019. PMID: 31006099

2

Sister-chromatid exchange inducing effect of smokeless tobacco using on T-lymphocyte chromosomes.

Ozkul Y, Erenmemisoglu A, Cucer N, Menevse A, Saatci CA. Ozkul Y, et al. Mutat Res. 1995 Apr;334(2):209-12. doi: 10.1016/0165-1161(95)90013-6. Mutat Res. 1995. PMID: 7885374

3

Do non-steroidal anti-inflammatory drugs induce sister chromatid exchanges in T lymphocytes?

Ozkul Y, Erenmemisoglu A, Ekecik A, Saatci C, Ozdamar S, Demirtas H. Ozkul Y, et al. J Int Med Res. 1996 Jan-Feb;24(1):84-7. doi: 10.1177/030006059602400110. J Int Med Res. 1996. PMID: 8674803 Clinical Trial.

4

Effect of zinc deficiency on chromosomal abnormalities in mice.

Ozkul Y, Dursun N, Erenmemişoğlu A, Süer C, Saatçi C. Ozkul Y, et al. Tohoku J Exp Med. 1996 Aug;179(4):247-51. doi: 10.1620/tjem.179.247. Tohoku J Exp Med. 1996. PMID: 8944425 Free article.

5

Female-to-male transsexual with 47,XXX karyotype.

Turan MT, Eşel E, Dündar M, Candemir Z, Baştürk M, Sofuoğlu S, Ozkul Y. Turan MT, et al. Among authors: ozkul y. Biol Psychiatry. 2000 Dec 1;48(11):1116-7. doi: 10.1016/s0006-3223(00)00954-9. Biol Psychiatry. 2000. PMID: 11094147

6

A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype.

Ozkul Y, Atabek ME, Dundar M, Kurtoglu S, Saatci C. Ozkul Y, et al. Ann Genet. 2002 Oct-Dec;45(4):181-3. doi: 10.1016/s0003-3995(02)01139-5. Ann Genet. 2002. PMID: 12668164

7

A family with two different chromosomal translocations.

Ozkul Y, Dundar M. Ozkul Y, et al. Ann Genet. 2002 Oct-Dec;45(4):185-7. doi: 10.1016/s0003-3995(02)01145-0. Ann Genet. 2002. PMID: 12668165

8

Associated anomalies in asymmetric crying facies and 22q11 deletion.

Akcakus M, Ozkul Y, Gunes T, Kurtoglu S, Cetin N, Kisaarslan AP, Dundar M. Akcakus M, et al. Among authors: ozkul y. Genet Couns. 2003;14(3):325-30. Genet Couns. 2003. PMID: 14577677

9

Triple-x syndrome accompanied by congenital adrenal hyperplasia: case report.

Kurtoğlu S, Atabek ME, Akçakuş M, Ozkul Y, Saatçi C. Kurtoğlu S, et al. Among authors: ozkul y. Turk J Pediatr. 2004 Oct-Dec;46(4):377-9. Turk J Pediatr. 2004. PMID: 15641277

10

Evaluation of the nucleolar organizer regions in Alzheimer's disease.

Dönmez-Altuntaş H, Akalin H, Karaman Y, Demirtaş H, Imamoğlu N, Ozkul Y. Dönmez-Altuntaş H, et al. Among authors: ozkul y. Gerontology. 2005 Sep-Oct;51(5):297-301. doi: 10.1159/000086365. Gerontology. 2005. PMID: 16110230

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