Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Deniz Ergec"'
Autor:
Korkut Ulucan, Ilter Guney, Aydan E. Özkaynakçi, Mustafa Uzan, Cigdem Ozkara, Deniz Ergec, Medine I. Gulcebi, Filiz Onat
Publikováno v:
Neurological Sciences. 36:397-401
Phenytoin has a widespread use in epilepsy treatment and is mainly metabolized by hepatic cytochrome P450 enzymes (CYP). We have investigated CYP2C9*2, CYP2C9*3, CYP2C19*2 and CYP2C19*3 allelic variants in a Turkish population of patients on phenytoi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d416e8494a3fac2abc764b78a15760ec
https://doi.org/10.1007/s10072-014-1961-8
https://doi.org/10.1007/s10072-014-1961-8
Autor:
Ahmet Ilter Güney, Teoman Akcay, Elif Cigdem Kaspar, Serap Turan, Deniz Kirac, Korkut Ulucan, Fatih Eren, Abdullah Bereket, Deniz Ergec, Gulsah Koc, Tulay Guran
Publikováno v:
Annals of Human Genetics. 78:399-409
Congenital adrenal hyperplasia (CAH) is a group of genetic endocrine disorders, caused by enzyme deficiencies in the conversion of cholesterol to cortisol. More than 90% of the cases have 21-hydroxylase deficiency (21-OHD). The clinical phenotype of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbe2db4284f3180b5f74f81837be8935
https://doi.org/10.1111/ahg.12083
https://doi.org/10.1111/ahg.12083
Autor:
Elif Cigdem Kaspar, Levent Türkeri, Tuba Avcilar, Deniz Kirac, Zehra Kaya, Korkut Ulucan, Ahmet Ilter Güney, Gulsah Koc, Deniz Ergec
Bladder carcinoma is the most common malignancy of the urinary tract. The major aim of the present study is to investigate the association between mitochondrial DNA (mtDNA) and p53 gene mutations in bladder carcinoma. A total of 30 patients with tran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5805fb4bc40702a7f47204c61d978685
https://hdl.handle.net/11424/241243
https://hdl.handle.net/11424/241243
Autor:
Deniz Ergec, Levent Türkeri, Hasan Hüseyin Tavukçu, Gulsah Koc, Ahmet Ilter Güney, Korkut Ulucan, Dilara Javadova, Deniz Kirac
Publikováno v:
Genetic Testing and Molecular Biomarkers. 16:672-678
Background: Mitochondrial DNA (mtDNA) mutations have been recently described in various tumors; however, data focusing on bladder cancer are scarce. To understand the significance of mtDNA mutations in bladder cancer development, we investigated the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70d258ee07cdde98304fca9bd7bc4455
https://doi.org/10.1089/gtmb.2011.0227
https://doi.org/10.1089/gtmb.2011.0227
Autor:
Deniz, Kirac, Ahmet Ilter, Guney, Teoman, Akcay, Tulay, Guran, Korkut, Ulucan, Serap, Turan, Deniz, Ergec, Gulsah, Koc, Fatih, Eren, Elif Cigdem, Kaspar, Abdullah, Bereket
Publikováno v:
Annals of human genetics. 78(6)
Congenital adrenal hyperplasia (CAH) is a group of genetic endocrine disorders, caused by enzyme deficiencies in the conversion of cholesterol to cortisol. More than 90% of the cases have 21-hydroxylase deficiency (21-OHD). The clinical phenotype of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c79e4e327f159ed5f89b116aaf10c897
https://pubmed.ncbi.nlm.nih.gov/25227725
https://pubmed.ncbi.nlm.nih.gov/25227725
Autor:
Ahmet Ilter Güney, Arzu Akcay, Deniz Kirac, Teoman Akcay, Deniz Ergec, Burak Ersoy, Korkut Ulucan
Publikováno v:
Volume: 2, Issue: 4 164-168
Clinical and Experimental Health Sciences
Clinical and Experimental Health Sciences
Objective: Non-syndromic cleft lip with/without palate (NSCL/P) takes part in multifactorial anomalies. In the present retrospective-descriptive study, we aimed to evaluate the distribution of Turkish children patients with non-syndromic cleft lip wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49d41f601cf2d7c30dd19cbdbfa5fe10
https://dergipark.org.tr/tr/pub/clinexphealthsci/issue/17851/187227
https://dergipark.org.tr/tr/pub/clinexphealthsci/issue/17851/187227
Autor:
H. Ozturhan, Gulsah Koc, M. Caner, Korkut Ulucan, Deniz Kirac, C. Kaspar, Ahmet Ilter Güney, Deniz Ergec, Mehmet Agirbasli
Publikováno v:
Genetics and molecular research : GMR. 12(4)
WOS: 000331608000279
PubMed ID: 24391037
Coronary artery disease (CAD) is a multifactorial disease influenced by genetic and environmental factors. Major risk factors of CAD are hypertension, hyperlipidemia, smoking, family history and obes
PubMed ID: 24391037
Coronary artery disease (CAD) is a multifactorial disease influenced by genetic and environmental factors. Major risk factors of CAD are hypertension, hyperlipidemia, smoking, family history and obes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55ceb3e283c2c60d49a8ad828cb1e8a7
https://pubmed.ncbi.nlm.nih.gov/24391037
https://pubmed.ncbi.nlm.nih.gov/24391037
Autor:
Hasan Hüseyin Tavukçu, Gulsah Koc, Dilara Javadova, Korkut Ulucan, Ahmet Ilter Güney, Deniz Ergec, Deniz Kirac, Tufan Tarcan
Publikováno v:
Genetics and molecular research : GMR. 11(2)
Infertility affects about 10-15% of all couples attempting pregnancy with infertility attributed to the male partner in approximately half of the cases. Proposed causes of male infertility include sperm motility disturbances, Y chromosome microdeleti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95d94c67d03bf5f1adb4337600a7ce07
https://pubmed.ncbi.nlm.nih.gov/22614272
https://pubmed.ncbi.nlm.nih.gov/22614272