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Items: 17


Identification of the variations in the CPT1B and CHKB genes along with the HLA-DQB1*06:02 allele in Turkish narcolepsy patients and healthy persons.

Cingoz S, Agilkaya S, Oztura I, Eroglu S, Karadeniz D, Evlice A, Altungoz O, Yilmaz H, Baklan B.

Genet Test Mol Biomarkers. 2014 Apr;18(4):261-8. doi: 10.1089/gtmb.2013.0391. Epub 2014 Feb 26.


The effect of the alternative solutions to formaldehyde and xylene on tissue processing.

Aydin I, Yörükoglu K, Cingöz S, Agilkaya S.

Indian J Pathol Microbiol. 2013 Jul-Sep;56(3):221-30. doi: 10.4103/0377-4929.120371.


Anxiety- and depression-like behavior are correlated with leptin and leptin receptor expression in prefrontal cortex of streptozotocin-induced diabetic rats.

Ates M, Dayi A, Kiray M, Sisman AR, Agilkaya S, Aksu I, Baykara B, Buyuk E, Cetinkaya C, Cingoz S, Uysal N.

Biotech Histochem. 2014 Apr;89(3):161-71. doi: 10.3109/10520295.2013.825319. Epub 2013 Sep 5.


An acute transverse myelitis attack after total body irradiation: a rare case.

Keklik M, Kaynar L, Yildirim A, Sivgin S, Eroglu C, Cingoz S, Pala C, Eser B, Cetin M, Unal A.

Case Rep Hematol. 2013;2013:523901. doi: 10.1155/2013/523901. Epub 2013 Jul 24.


A novel missense mutation (N78D) in a family with von Hippel-Lindau disease with central nervous system haemangioblastomas, pancreatic and renal cysts.

Cingoz S, van der Luijt RB, Kurt E, Apaydin M, Akkol I, Ozgen MH.

Fam Cancer. 2013 Mar;12(1):111-7. doi: 10.1007/s10689-012-9586-7.


Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α.

Ceran C, Cokol M, Cingoz S, Tasan I, Ozturk M, Yagci T.

BMC Cancer. 2012 Oct 4;12:450. doi: 10.1186/1471-2407-12-450.


Maternal aerobic exercise during pregnancy can increase spatial learning by affecting leptin expression on offspring's early and late period in life depending on gender.

Dayi A, Agilkaya S, Ozbal S, Cetin F, Aksu I, Gencoglu C, Cingoz S, Pekcetin C, Tugyan K, Kayatekin BM, Uysal N.

ScientificWorldJournal. 2012;2012:429803. doi: 10.1100/2012/429803. Epub 2012 Sep 16.


Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects.

Cingöz S, Bache I, Bjerglund L, Ropers HH, Tommerup N, Jensen H, Brøndum-Nielsen K, Tümer Z.

Am J Med Genet A. 2011 Jan;155A(1):203-6. doi: 10.1002/ajmg.a.33766.


TLR polymorphisms in FMF: association of TLR-2 (Arg753Gln) and TLR-4 (Asp299Gly, Thre399Ile) polymorphisms and myeloid cell TLR-2 and TLR-4 expression with the development of secondary amyloidosis in FMF.

Soylu A, Ateş H, Cingöz S, Türkmen M, Demir BK, Tunca M, Sakızlı M, Cirit M, Ersoy R, Ulgenalp A, Kavukçu S.

Inflammation. 2011 Oct;34(5):379-87. doi: 10.1007/s10753-010-9245-9.


TLR-2 Arg753Gln, TLR-4 Asp299Gly, and TLR-4 Thr399Ile polymorphisms in Henoch Schonlein purpura with and without renal involvement.

Soylu A, Kizildağ S, Kavukçu S, Cingöz S, Türkmen M, Demir BK, Sakizli M.

Rheumatol Int. 2010 Mar;30(5):667-70. doi: 10.1007/s00296-009-1052-y. Epub 2009 Jul 12.


A novel subtype of distal symphalangism affecting only the 4th finger.

Kjaer KW, Tiner M, Cingoz S, Karatosun V, Tommerup N, Mundlos S, Gunal I.

Am J Med Genet A. 2009 Jul;149A(7):1571-3. doi: 10.1002/ajmg.a.32905. No abstract available.


Familial pericentric inversion chromosome 3 and R448C mutation of CYP11B1 gene in Turkish kindred with 11beta-hydroxylase deficiency.

Cingöz S, Ozkan B, Döneray H, Sakizli M.

J Endocrinol Invest. 2007 Apr;30(4):285-91.


4q35 deletion and 10p15 duplication associated with immunodeficiency.

Cingoz S, Bisgaard AM, Bache I, Bryndorf T, Kirchoff M, Petersen W, Ropers HH, Maas N, Van Buggenhout G, Tommerup N, Tümer Z.

Am J Med Genet A. 2006 Oct 15;140(20):2231-5.


Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter.

Sogaard M, Tümer Z, Hjalgrim H, Hahnemann J, Friis B, Ledaal P, Pedersen VF, Baekgaard P, Tommerup N, Cingöz S, Duno M, Brondum-Nielsen K.

BMC Med Genet. 2005 May 17;6:21.


An excess of chromosome 1 breakpoints in male infertility.

Bache I, Assche EV, Cingoz S, Bugge M, Tümer Z, Hjorth M, Lundsteen C, Lespinasse J, Winther K, Niebuhr A, Kalscheuer V, Liebaers I, Bonduelle M, Tournaye H, Ayuso C, Barbi G, Blennow E, Bourrouillou G, Brondum-Nielsen K, Bruun-Petersen G, Croquette MF, Dahoun S, Dallapiccola B, Davison V, Delobel B, Duba HC, Duprez L, Ferguson-Smith M, Fitzpatrick DR, Grace E, Hansmann I, Hultén M, Jensen PK, Jonveaux P, Kristoffersson U, Lopez-Pajares I, McGowan-Jordan J, Murken J, Orera M, Parkin T, Passarge E, Ramos C, Rasmussen K, Schempp W, Schubert R, Schwinger E, Shabtai F, Smith K, Stallings R, Stefanova M, Tranebjerg L, Turleau C, van der Hagen CB, Vekemans M, Vokac NK, Wagner K, Wahlstroem J, Zelante L, Tommerup N.

Eur J Hum Genet. 2004 Dec;12(12):993-1000.


DNA copy number changes detected by comparative genomic hybridization and their association with clinicopathologic parameters in breast tumors.

Cingoz S, Altungoz O, Canda T, Saydam S, Aksakoglu G, Sakizli M.

Cancer Genet Cytogenet. 2003 Sep;145(2):108-14.

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