Publications by authors named "Sultan Cingoz"

Claim this Profile
F
Functional divergence of the two Elongator subcomplexes during neurodevelopment.
Monika Gaik, Marija Kojic, Megan R Stegeman, Tülay Öncü-Öner, Anna Kościelniak

EMBO Mol Med· July 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel biallelic variants affecting the OTU domain of the gene OTUD6B associate with severe intellectual disability syndrome and molecular dynamics simulations.
Sultan Cingöz, Didem Soydemir, Tülay Öncü Öner, Ezgi Karaca, Burcu Özden

Eur J Med Genet· June 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development.
Tulay Oncu Oner, Aycan Unalp, Semra Hiz, Erhan Bayram, Ismail Kaytan, Sultan Cingoz

Epileptic Disord· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria.
Tülay Öncü-Öner, Aycan Ünalp, İlknur Porsuk-Doru, Sinem Ağılkaya, Handan Güleryüz

Turk J Pediatr· February 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Exercise increases leptin levels correlated with IGF-1 in hippocampus and prefrontal cortex of adolescent male and female rats.
Nazan Uysal, Sinem Agilkaya, Ali Riza Sisman, Ulas Mehmet Camsari, Celal Gencoglu, Sultan Cingoz

J Chem Neuroanat· April 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The effect of the alternative solutions to formaldehyde and xylene on tissue processing.
Ilgin Aydin, Kutsal Yörükoglu, Sultan Cingöz, Sinem Agilkaya

Indian J Pathol Microbiol· April 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
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.
Sultan Cingoz, Sinem Agilkaya, Ibrahim Oztura, Secil Eroglu, Derya Karadeniz

Genet Test Mol Biomarkers· April 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
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.
Ayfer Dayi, Sinem Agilkaya, Seda Ozbal, Ferihan Cetin, Ilkay Aksu, Sultan Cingoz

ScientificWorldJournal· February 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α.
Ceyhan Ceran, Murat Cokol, Sultan Cingoz, Ipek Tasan, Mehmet Ozturk

BMC Cancer· October 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
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.
Alper Soylu, Halil Ateş, Sultan Cingöz, Mehmet Türkmen, Belde Kasap Demir

Inflammation· October 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects.
Sultan Cingöz, Iben Bache, Lise Bjerglund, Hans-Hilger Ropers, Niels Tommerup

Am J Med Genet A· January 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
TLR-2 Arg753Gln, TLR-4 Asp299Gly, and TLR-4 Thr399Ile polymorphisms in Henoch Schonlein purpura with and without renal involvement.
Alper Soylu, Sefa Kizildağ, Salih Kavukçu, Sultan Cingöz, Mehmet Türkmen

Rheumatol Int· March 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel subtype of distal symphalangism affecting only the 4th finger.
Klaus W Kjaer, Mehmet Tiner, Sultan Cingoz, Vasfi Karatosun, Niels Tommerup

Am J Med Genet A· July 2009

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
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.
Marie Sogaard, Zeynep Tümer, Helle Hjalgrim, Johanne Hahnemann, Birgitte Friis

BMC Med Genet· May 2005

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An excess of chromosome 1 breakpoints in male infertility.
Iben Bache, Elvire Van Assche, Sultan Cingoz, Merete Bugge, Zeynep Tümer

Eur J Hum Genet· December 2004

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
DNA copy number changes detected by comparative genomic hybridization and their association with clinicopathologic parameters in breast tumors.
Sultan Cingoz, Oguz Altungoz, Tulay Canda, Serdar Saydam, Gazanfer Aksakoglu

Cancer Genet Cytogenet· September 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis