Pehlivan D - Search Results

1

Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma.

Ma M, Ganapathi M, Zheng Y, Tan KL, Kanca O, Bove KE, Quintanilla N, Sag SO, Temel SG, LeDuc CA, McPartland AJ, Pereira EM, Shen Y, Hagen J, Thomas CP, Nguyen Galván NT, Pan X, Lu S, Rosenfeld JA, Calame DG, Wangler MF, Lupski JR, Pehlivan D, Hertel PM, Chung WK, Bellen HJ. Ma M, et al. Among authors: pehlivan d. Genet Med. 2024 Jul;26(7):101125. doi: 10.1016/j.gim.2024.101125. Epub 2024 Mar 21. Genet Med. 2024. PMID: 38522068 Free PMC article.

2

Metastasis: genetics, mechanism, and diagnostic and therapeutic strategies.

Gunduz M, Gunduz E, Beder L, Pehlivan D, Hatipoglu OF, Kachhap S, Grenman R. Gunduz M, et al. Among authors: pehlivan d. J Oncol. 2012;2012:390835. doi: 10.1155/2012/390835. Epub 2012 Dec 30. J Oncol. 2012. PMID: 23326264 Free PMC article. No abstract available.

3

First Case of MELAS Syndrome Presenting with Local Brain Edema Requiring Decompressive Craniectomy.

Yesilbas O, Sengenc E, Olbak ME, Bako D, Nizam OG, Seyithanoglu MH, Pehlivan D, Ceylaner S, Icagasioglu D, Aydin K. Yesilbas O, et al. Among authors: pehlivan d. Turk Neurosurg. 2022;32(1):155-159. doi: 10.5137/1019-5149.JTN.34196-21.4. Turk Neurosurg. 2022. PMID: 34664704 Free article.

4

Involvement of EphA2 in head and neck squamous cell carcinoma: mRNA expression, loss of heterozygosity and immunohistochemical studies.

Rivera RS, Gunduz M, Nagatsuka H, Gunduz E, Cengiz B, Fukushima K, Beder LB, Pehlivan D, Yamanaka N, Shimizu K, Nagai N. Rivera RS, et al. Among authors: pehlivan d. Oncol Rep. 2008 May;19(5):1079-84. Oncol Rep. 2008. PMID: 18425361

5

Downregulation of ING3 mRNA expression predicts poor prognosis in head and neck cancer.

Gunduz M, Beder LB, Gunduz E, Nagatsuka H, Fukushima K, Pehlivan D, Cetin E, Yamanaka N, Nishizaki K, Shimizu K, Nagai N. Gunduz M, et al. Among authors: pehlivan d. Cancer Sci. 2008 Mar;99(3):531-8. doi: 10.1111/j.1349-7006.2007.00708.x. Epub 2007 Dec 15. Cancer Sci. 2008. PMID: 18081876 Free PMC article.

6

The role of GSTM1 gene polymorphisms in lung cancer development in Turkish population.

Demir A, Altin S, Pehlivan D, Demir M, Yakar F, Seyhan EC, Dincer SI. Demir A, et al. Among authors: pehlivan d. J Carcinog. 2007 Sep 26;6:13. doi: 10.1186/1477-3163-6-13. J Carcinog. 2007. PMID: 17897446 Free PMC article.

7

Loss of heterozygosity at chromosome 14q is associated with poor prognosis in head and neck squamous cell carcinomas.

Pehlivan D, Gunduz E, Gunduz M, Nagatsuka H, Beder LB, Cengiz B, Rivera RS, Fukushima K, Palanduz S, Ozturk S, Yamanaka N, Shimizu K. Pehlivan D, et al. J Cancer Res Clin Oncol. 2008 Dec;134(12):1267-76. doi: 10.1007/s00432-008-0423-1. Epub 2008 Jun 3. J Cancer Res Clin Oncol. 2008. PMID: 18521630

8

Deletion mapping of chromosome 4q22-35 and identification of four frequently deleted regions in head and neck cancers.

Cetin E, Cengiz B, Gunduz E, Gunduz M, Nagatsuka H, Bekir-Beder L, Fukushima K, Pehlivan D, N MO, Nishizaki K, Shimizu K, Nagai N. Cetin E, et al. Among authors: pehlivan d. Neoplasma. 2008;55(4):299-304. Neoplasma. 2008. PMID: 18505340

9

Cornelia de Lange syndrome case due to genomic rearrangements including NIPBL.

Ratajska M, Wierzba J, Pehlivan D, Xia Z, Brundage EK, Cheung SW, Stankiewicz P, Lupski JR, Limon J. Ratajska M, et al. Among authors: pehlivan d. Eur J Med Genet. 2010 Nov-Dec;53(6):378-82. doi: 10.1016/j.ejmg.2010.08.002. Epub 2010 Aug 18. Eur J Med Genet. 2010. PMID: 20727427

10

Evidence for disease penetrance relating to CNV size: Pelizaeus-Merzbacher disease and manifesting carriers with a familial 11 Mb duplication at Xq22.

Carvalho CM, Bartnik M, Pehlivan D, Fang P, Shen J, Lupski JR. Carvalho CM, et al. Among authors: pehlivan d. Clin Genet. 2012 Jun;81(6):532-41. doi: 10.1111/j.1399-0004.2011.01716.x. Epub 2011 Jun 20. Clin Genet. 2012. PMID: 21623770 Free PMC article.

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