Pehlivan D - Search Results

1

Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy.

Morales-Rosado JA, Schwab TL, Macklin-Mantia SK, Foley AR, Pinto E Vairo F, Pehlivan D, Donkervoort S, Rosenfeld JA, Boyum GE, Hu Y, Cong ATQ, Lotze TE, Mohila CA, Saade D, Bharucha-Goebel D, Chao KR, Grunseich C, Bruels CC, Littel HR, Estrella EA, Pais L, Kang PB, Zimmermann MT, Lupski JR, Lee B, Schellenberg MJ, Clark KJ, Wierenga KJ, Bönnemann CG, Klee EW. Morales-Rosado JA, et al. Among authors: pehlivan d. Am J Hum Genet. 2023 Jun 1;110(6):989-997. doi: 10.1016/j.ajhg.2023.04.006. Epub 2023 May 10. Am J Hum Genet. 2023. PMID: 37167966 Free PMC article.

2

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

3

Esophagus cancer and IgA deficiency in a patient with Dubowitz syndrome: a case report.

Turkbeyler IH, Pehlivan Y, Comez G, Pehlivan D, Sevinc A, Kalender ME, Karakok M, Camci C. Turkbeyler IH, et al. Among authors: pehlivan d, pehlivan y. Tokai J Exp Clin Med. 2011 Jul 20;36(2):29-30. Tokai J Exp Clin Med. 2011. PMID: 21769769 Free article.

4

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.

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

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

7

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.

8

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

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

Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy.

McLaughlin HM, Sakaguchi R, Liu C, Igarashi T, Pehlivan D, Chu K, Iyer R, Cruz P, Cherukuri PF, Hansen NF, Mullikin JC; NISC Comparative Sequencing Program; Biesecker LG, Wilson TE, Ionasescu V, Nicholson G, Searby C, Talbot K, Vance JM, Züchner S, Szigeti K, Lupski JR, Hou YM, Green ED, Antonellis A. McLaughlin HM, et al. Among authors: pehlivan d. Am J Hum Genet. 2010 Oct 8;87(4):560-6. doi: 10.1016/j.ajhg.2010.09.008. Am J Hum Genet. 2010. PMID: 20920668 Free PMC article.

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