Cingöz S - Search Results

1

Functional divergence of the two Elongator subcomplexes during neurodevelopment.

Gaik M, Kojic M, Stegeman MR, Öncü-Öner T, Kościelniak A, Jones A, Mohamed A, Chau PYS, Sharmin S, Chramiec-Głąbik A, Indyka P, Rawski M, Biela A, Dobosz D, Millar A, Chau V, Ünalp A, Piper M, Bellingham MC, Eichler EE, Nickerson DA, Güleryüz H, Abbassi NEH, Jazgar K, Davis MJ, Mercimek-Andrews S, Cingöz S, Wainwright BJ, Glatt S. Gaik M, et al. Among authors: cingoz s. EMBO Mol Med. 2022 Jul 7;14(7):e15608. doi: 10.15252/emmm.202115608. Epub 2022 Jun 13. EMBO Mol Med. 2022. PMID: 35698786 Free PMC article.

2

Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations.

Cingöz S, Soydemir D, Öner TÖ, Karaca E, Özden B, Kurul SH, Bayram E; University of Washington Center for Mendelian Genomics; Coe BP, Nickerson DA, Eichler EE. Cingöz S, et al. Eur J Med Genet. 2022 Jun;65(6):104497. doi: 10.1016/j.ejmg.2022.104497. Epub 2022 Apr 14. Eur J Med Genet. 2022. PMID: 35430327 Free PMC article.

3

GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria.

Öncü-Öner T, Ünalp A, Porsuk-Doru İ, Ağılkaya S, Güleryüz H, Saraç A, Ergüner B, Yüksel B, Hız-Kurul S, Cingöz S. Öncü-Öner T, et al. Among authors: cingoz s. Turk J Pediatr. 2018;60(3):229-237. doi: 10.24953/turkjped.2018.03.001. Turk J Pediatr. 2018. PMID: 30511534 Free article.

4

OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development.

Oner TO, Unalp A, Hiz S, Bayram E, Kaytan I, Cingoz S. Oner TO, et al. Among authors: cingoz s. Epileptic Disord. 2021 Dec 1;23(6):843-853. doi: 10.1684/epd.2021.1349. Epileptic Disord. 2021. PMID: 34704946

5

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

Aydin I, Yörükoglu K, Cingöz S, Agilkaya S. Aydin I, et al. Among authors: cingoz s. Indian J Pathol Microbiol. 2013 Jul-Sep;56(3):221-30. doi: 10.4103/0377-4929.120371. Indian J Pathol Microbiol. 2013. PMID: 24152498

6

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. Cingoz S, et al. Genet Test Mol Biomarkers. 2014 Apr;18(4):261-8. doi: 10.1089/gtmb.2013.0391. Epub 2014 Feb 26. Genet Test Mol Biomarkers. 2014. PMID: 24571861 Free PMC article.

7

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. Dayi A, et al. Among authors: cingoz s. ScientificWorldJournal. 2012;2012:429803. doi: 10.1100/2012/429803. Epub 2012 Sep 16. ScientificWorldJournal. 2012. PMID: 23028249 Free PMC article.

8

Exercise increases leptin levels correlated with IGF-1 in hippocampus and prefrontal cortex of adolescent male and female rats.

Uysal N, Agilkaya S, Sisman AR, Camsari UM, Gencoglu C, Dayi A, Aksu I, Baykara B, Cingoz S, Kiray M. Uysal N, et al. Among authors: cingoz s. J Chem Neuroanat. 2017 Apr;81:27-33. doi: 10.1016/j.jchemneu.2017.02.004. Epub 2017 Feb 4. J Chem Neuroanat. 2017. PMID: 28179125

9

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. Cingoz S, et al. Fam Cancer. 2013 Mar;12(1):111-7. doi: 10.1007/s10689-012-9586-7. Fam Cancer. 2013. PMID: 23224817

10

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. Cingoz S, et al. Am J Med Genet A. 2006 Oct 15;140(20):2231-5. doi: 10.1002/ajmg.a.31431. Am J Med Genet A. 2006. PMID: 16964622

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