Works matching AU Pehlivan, Sacide

Results: 96

Investigation of leukocyte telomere length and hTERT gene MNS16A VNTR variant in microtia patients.

Published in:

Experimental Biomedical Research, 2025, v. 8, n. 1, p. 8, doi. 10.30714/j-ebr.2025.232

By:

Sayın, Sevde Hasanoğlu;
Büyükgüral, Berker;
Tunçel, Fatıma Ceren;
Oyacı, Yasemin;
Bekerecioğlu, Mehmet;
Pehlivan, Sacide

Publication type:

Article

DNA ploidy, proliferative activity, and concanavalin A reactivity in breast cancer.

Published in:

Journal of Surgical Oncology, 1994, v. 56, n. 1, p. 21, doi. 10.1002/jso.2930560106

By:

Paydas, Semra;
Sarpel, Suleyman;
Gilman-Sachs, Alice;
Tuncer, Ilhan;
Pehlivan, Sacide;
Tunali, Nurdan;
Zorludemir, Suzan;
Burgut, Refik;
Kucuk, Omer

Publication type:

Article

Role of cytokine gene (IFN-γ, TNF-α, TGF-β1, IL-6, and IL-10) polymorphisms in pathogenesis of acute rheumatic fever in Turkish children.

Published in:

2012

By:

Col-Araz N;
Pehlivan S;
Baspinar O;
Oguzkan-Balci S;
Sever T;
Balat A;
Col-Araz, Nilgun;
Pehlivan, Sacide;
Baspinar, Osman;
Oguzkan-Balci, Sibel;
Sever, Tugce;
Balat, Ayse

Publication type:

journal article

Role of cytokine gene (IFN-γ, TNF-α, TGF-β1, IL-6, and IL-10) polymorphisms in pathogenesis of acute rheumatic fever in Turkish children.

Published in:

European Journal of Pediatrics, 2012, v. 171, n. 7, p. 1103, doi. 10.1007/s00431-012-1689-5

By:

Col-Araz, Nilgun;
Pehlivan, Sacide;
Baspinar, Osman;
Oguzkan-Balci, Sibel;
Sever, Tugce;
Balat, Ayse

Publication type:

Article

Evaluation of gene-gene interaction between the interleukin (IL)-2 and IL-2RA gene polymorphisms in schizophrenia patients in the Turkish Population.

Published in:

Neurosciences, 2024, v. 29, n. 1, p. 51, doi. 10.17712/nsj.2024.1.20230075

By:

Ozdilli, Kursat;
Aytac, Hasan Mervan;
Tuncel, Fatima Ceren;
Oyaci, Yasemin;
Pehlivan, Mustafa;
Pehlivan, Sacide

Publication type:

Article

Association of intron 4 VNTR polymorphism in the NOS3 gene with rapid cycling and treatment resistance in bipolar disorder: a case-control study.

Published in:

Neurosciences, 2022, v. 27, n. 4, p. 229, doi. 10.17712/nsj.2022.4.20220040

By:

Aytac, Hasan M.;
Pehlivan, Mustafa;
Oyaci, Yasemin;
Pehlivan, Sacide

Publication type:

Article

COMT Val158Met polymorphism is associated with ecstasy (MDMA)-induced psychotic symptoms in the Turkish population.

Published in:

Neurosciences, 2022, v. 27, n. 1, p. 24, doi. 10.17712/nsj.2022.1.20210045

By:

Aytac, Hasan Mervan;
Oyaci, Yasemin;
Aydin, Pinar Cetinay;
Pehlivan, Mustafa;
Pehlivan, Sacide

Publication type:

Article

Investigation of inflammation related gene polymorphism of the mannose-binding lectin 2 in schizophrenia and bipolar disorder.

Published in:

Neurosciences, 2021, v. 26, n. 4, p. 346, doi. 10.17712/nsj.2021.4.20200050

By:

Aytac, Hasan M.;
Yazar, Menekse S.;
Erol, Ayse;
Pehlivan, Sacide

Publication type:

Article

Association of macrophage migration inhibitory factor and mannose-binding lectin-2 gene polymorphisms in acute rheumatic fever.

Published in:

Cardiology in the Young, 2013, v. 23, n. 4, p. 486, doi. 10.1017/S1047951112000972

By:

Col-Araz, Nilgun;
Pehlivan, Sacide;
Baspinar, Osman;
Sever, Tugce;
Oguzkan-Balci, Sibel;
Balat, Ayse

Publication type:

Article

Interleukin-1 receptor antagonist (IL-1RA) and interleukin-4 (IL-4) variable number of tandem repeat polymorphisms in schizophrenia and bipolar disorder: an association study in Turkish population.

Published in:

Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00341-6

By:

Pehlivan, Sacide;
Oyaci, Yasemin;
Tuncel, Fatima Ceren;
Aytac, Hasan Mervan

Publication type:

Article

Dopamine D4 Receptor Gene Exon III VNTR Variant Influences Smoking Status in Turkish Population.

Published in:

Archives of Neuropsychiatry / Nöropsikiyatri Arşivi, 2019, v. 56, n. 4, p. 248, doi. 10.29399/npa.23408

By:

UYSAL, Mehmet Atilla;
SEVER, Ülgen;
NURSAL, Ayşe Feyda;
PEHLİVAN, Sacide

Publication type:

Article

Genetic contributing factors to substance abuse: an association study between eNOS gene polymorphisms and cannabis addiction in a Turkish population.

Published in:

Australian Journal of Forensic Sciences, 2016, v. 48, n. 6, p. 676, doi. 10.1080/00450618.2015.1112428

By:

Baransel Isir, Aysun;
Nacak, Muradiye;
Balci, Sibel Oguzkan;
Aynacioglu, A. Sukru;
Pehlivan, Sacide

Publication type:

Article

Relationship between the 1359 G/A polymorphism of the Central Cannabinoid Receptor 1 (CNR1) gene and susceptibility to cannabis addiction in a Turkish population.

Published in:

Australian Journal of Forensic Sciences, 2015, v. 47, n. 2, p. 230, doi. 10.1080/00450618.2014.936895

By:

Baransel Isir, Aysun;
Nacak, Muradiye;
Oguzkan Balci, Sibel;
Pehlivan, Sacide;
Kul, Seval;
Benlier, Necla;
Sukru Aynacioglu, A.

Publication type:

Article

The value of XPD and XRCC1 genotype polymorphisms to predict clinical outcome in metastatic colorectal carcinoma patients with irinotecan-based regimens.

Published in:

Journal of Cancer Research & Clinical Oncology, 2010, v. 136, n. 6, p. 803, doi. 10.1007/s00432-009-0720-3

By:

Artac, Mehmet;
Bozcuk, Hakan;
Pehlivan, Sacide;
Akcan, Songül;
Mustafa Pehlivan;
Tugce Sever;
Mustafa Ozdogan;
Burhan Savas

Publication type:

Article

Mannose-Binding Lectin 2 Gene Polymorphism during Pandemic: COVID-19 Family.

Published in:

Global Medical Genetics, 2022, v. 9, n. 2, p. 185, doi. 10.1055/s-0042-1743258

By:

Tukek, Tufan;
Pehlivan, Sacide;
Oyaci, Yasemin;
Isoglu-Alkac, Ummuhan

Publication type:

Article

Association of the TNF-α, IL-2, and IL-2RB gene variants with susceptibility to psoriasis in a Turkish cohort.

Published in:

Central European Journal of Immunology, 2018, v. 43, n. 1, p. 50, doi. 10.5114/ceji.2018.74873

By:

GULEL, ASLIHAN;
INALOZ, HUSEYIN SERHAT;
NURSAL, AYSE FEYDA;
SEVER, TUGCE;
PEHLIVAN, SACIDE

Publication type:

Article

DNA Methylation Pattern of Gene Promoters of MB-COMT, DRD2, and NR3C1 in Turkish Patients Diagnosed with Schizophrenia.

Published in:

Clinical Psychopharmacology & Neuroscience, 2022, v. 20, n. 4, p. 685, doi. 10.9758/cpn.2022.20.4.685

By:

Aytac, Hasan Mervan;
Oyaci, Yasemin;
Pehlivan, Mustafa;
Pehlivan, Sacide

Publication type:

Article

Importance of mannose-binding lectin2 polymorphism (rs1800450) in infections in children.

Published in:

Biomarkers, 2022, v. 27, n. 1, p. 44, doi. 10.1080/1354750X.2021.2003432

By:

Uysalol, Metin;
Gumus, Suheyla;
Yildiz, Raif;
Pasli Uysalol, Ezgi;
Pehlivan, Sacide;
Pehlivan, Mustafa;
Serin, Istemi

Publication type:

Article

Investigation of interleukin- 12, interleukin-17 and interleukin-23 receptor gene polymorphisms in alopecia areata.

Published in:

Journal of International Medical Research, 2015, v. 43, n. 4, p. 526, doi. 10.1177/0300060514549784

By:

Aytekin, Nesrin;
Akcali, Cenk;
Pehlivan, Sacide;
Kirtak, Necmettin;
Inaloz, Serhat

Publication type:

Article

LEP rs7799039 and LEPR rs1137101 gene variants are not associated with clinical features in patients with metabolic syndrome in the Turkish population.

Published in:

Laboratory Medicine, 2025, v. 56, n. 1, p. 37, doi. 10.1093/labmed/lmae061

By:

Jabbarli, Marjan;
Senkal, Naci;
Tuncel, Fatima Ceren;
Oyaci, Yasemin;
Dirim, Merve Guzel;
Kose, Murat;
Pehlivan, Sacide;
Medetalibeyoglu, Alpay

Publication type:

Article

GENETIC POLYMORPHISMS IN 15 STR LOCI IN THE TURKISH POPULATION LIVING IN ISTANBUL PROVINCE.

Published in:

Nobel Medicus Journal, 2022, v. 18, n. 1, p. 54

By:

Ozdilli, Kursat;
Ogret, Yeliz Duvarcı;
Oguz, Rustu;
Issever, Halim;
Yokes, Mehmet Baki;
Çiftçi, Hayriye Senturk;
Sel, Figen Abatay;
Kivanc, Demet;
Cinar, Cigdem Kekik;
Pehlivan, Sacide;
Oguz, Fatma Savran

Publication type:

Article

Medication-related osteonecrosis of the jaw (MRONJ) and eNOS Polymorphisms in multiple myeloma patients: a single center experience.

Published in:

BMC Oral Health, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12903-021-01634-9

By:

Taş Ozyurtseven, Betul;
Serin, Istemi;
Nursal, Ayse Feyda;
Pehlivan, Sacide;
Pehlivan, Mustafa

Publication type:

Article

Macrophage Migration Inhibitory Factor - 173 G/C Polymorphism is Associated With The Age of Onset and Insight in Schizophrenia in the Turkish Population.

Published in:

Neurological Research, 2021, v. 43, n. 12, p. 977, doi. 10.1080/01616412.2021.1948748

By:

Aytac, Hasan Mervan;
Oyaci, Yasemin;
Yazar, Menekse Sila;
Pehlivan, Sacide

Publication type:

Article

ASSOCIATING eNOS GENE VARIANTS WITH COVID-19 SUSCEPTIBILITY IN THE TURKISH POPULATION.

Published in:

Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi, 2023, v. 86, n. 1, p. 1, doi. 10.26650/IUITFD.1211888

By:

ŞENKAL, Naci;
OYACI, Yasemin;
CEBECİ, Timurhan;
KONYAOĞLU, Hilal;
KÖSE, Murat;
ÖNEL, Mustafa;
MEDETALİBEYOĞLU, Alpay;
YEŞİL SAYIN, Gözde;
PEHLİVAN, Mustafa;
PEHLİVAN, Sacide;
İŞOĞLU-ALKAÇ, Ümmihan;
TÜKEK, Tufan

Publication type:

Article

The suppressor of cytokine signaling-1 (SOCS1) gene polymorphism and promoter methylation correlate with the course of COVID-19.

Published in:

Pathogens & Global Health, 2023, v. 117, n. 4, p. 392, doi. 10.1080/20477724.2022.2151861

By:

Tukek, Tufan;
Pehlivan, Sacide;
Medetalibeyoglu, Alpay;
Serin, Istemi;
Oyacı, Yasemin;
Arıcı, Huzeyfe;
Senkal, Naci;
Pehlivan, Mustafa;
Isoglu-Alkac, Ummuhan;
Kose, Murat

Publication type:

Article

Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (–) patients.

Published in:

Pathogens & Global Health, 2022, v. 116, n. 3, p. 178, doi. 10.1080/20477724.2021.1984726

By:

Pehlivan, Sacide;
Köse, Murat;
Mese, Sevim;
Serin, Istemi;
Senkal, Naci;
Oyacı, Yasemin;
Medetalibeyoglu, Alpay;
Pehlivan, Mustafa;
Sayın, Gözde Yesil;
Isoglu-Alkac, Ummihan;
Tukek, Tufan

Publication type:

Article

Associations of XRCC4, eNOS, and PER3 VNTR variants with Childhood Acute Lymphoblastic Leukemia in Turkish Patients.

Published in:

Medical Journal of Bakirkoy, 2022, v. 18, n. 4, p. 463, doi. 10.4274/BMJ.galenos.2022.2021.11-14

By:

Oğuz, Rüştü;
Gökçe, Müge;
Pehlivan, Sacide;
Oyacı, Yasemin;
Çiftçi, Hayriye Şentürk;
Atay, Avni;
Karakaş, Zeynep;
Aydın, Filiz

Publication type:

Article

The MIF rs755622 Variant may Increase Susceptibility of Breast Cancer but not Gastrointestinal Cancer in a Turkish Population.

Published in:

Turkish Journal of Oncology / Türk Onkoloji Dergisi, 2020, v. 35, n. 3, p. 283, doi. 10.5505/tjo.2020.2186

By:

PEHLİVAN, Sacide;
IŞIKSAÇAN, Nilgün;
PEHLİVAN, Mustafa;
GÜNALDI, Meral;
OYACI, Yasemin;
NURSAL, Ayşe Feyda

Publication type:

Article

Effect of the uncoupling protein-2 (UCP-2) and nuclear receptor subfamily 3 group C member 1 (NR3C1) genes on treatment efficacy and survival in patients with multiple myeloma: a single-center study.

Published in:

BMC Research Notes, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13104-021-05758-7

By:

Demir, Ilknur;
Pehlivan, Sacide;
Okan, Vahap;
Sahin, Handan Haydaroglu;
Durusoy, Salih Sertaç;
Serin, Istemi;
Oyaci, Yasemin;
Pehlivan, Mustafa

Publication type:

Article

The miRNA 196a2 rs11614913 variant has prognostic impact on Turkish patients with multiple myeloma.

Published in:

BMC Research Notes, 2020, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13104-020-05392-9

By:

Kirik, Melya Pelin;
Pehlivan, Mustafa;
Nursal, Ayse Feyda;
Oyaci, Yasemin;
Pehlivan, Sacide;
SERIN, Istemi

Publication type:

Article

Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: a preliminary study.

Published in:

2008

By:

Akcali A;
Tataroglu C;
Erdal E;
Aydin N;
Pehlivan S;
Aylin, Akcali;
Cengiz, Tataroglu;
Emin, Erdal;
Neriman, Aydin;
Sacide, Pehlivan

Publication type:

journal article

Serotonin transporter gene polymorphisms in patients with chronic tension-type headache: A preliminary study.

Published in:

Neurology India, 2008, v. 56, n. 2, p. 156

By:

Aylin, Akcali;
Cengiz, Tataroglu;
Emin, Erdal;
Neriman, Aydin;
Sacide, Pehlivan

Publication type:

Article

Is pregnancy loss after amniocentesis related to the volume of amniotic fluid obtained?

Published in:

Archives of Gynecology & Obstetrics, 2009, v. 279, n. 3, p. 357, doi. 10.1007/s00404-008-0740-2

By:

Cebesoy, Fatma Bahar;
Balat, Ozcan;
Pehlivan, Sacide;
Kutlar, Irfan;
Dikensoy, Ebru;
Ugur, Mete Gurol

Publication type:

Article

Glutathione peroxidase and catalase enzyme gene polymorphisms in profound congenital hearing loss.

Published in:

ENT Updates, 2017, v. 7, n. 3, p. 126, doi. 10.2399/jmu.2017003003

By:

Tunç, Orhan;
Baysal, Elif;
Balcı, Sibel Oğuzkan;
Mumbuç, Semih;
Tunç, Nihal Güngör;
Pehlivan, Sacide;
Kanlıkama, Muzaffer

Publication type:

Article

Cytokine gene variants/expressions and non-syndromic microtia - is there a link?

Published in:

ENT Updates, 2017, v. 7, n. 2, p. 62, doi. 10.2399/jmu.2017002007

By:

Nursal, Ayşe Feyda;
Bekerecioğlu, Mehmet;
Pehlivan, Sacide;
Sever, Tuğçe;
Büyükgüral, Berker

Publication type:

Article

The roles of endothelial nitric oxide synthase (eNOS) and myeloperoxidase (MPO) genes in microtia.

Published in:

ENT Updates, 2016, v. 6, n. 3, p. 121, doi. 10.2399/jmu.2016003008

By:

Büyükgüral, Berker;
Pehlivan, Sacide;
Nursal, Ayşe Feyda;
Bekerecioğlu, Mehmet

Publication type:

Article

Cytokine gene polymorphisms and expression in Turkish pediatric cochlear implant patients.

Published in:

ENT Updates, 2016, v. 6, n. 1, p. 1, doi. 10.2399/jmu.2016001002

By:

Baysal, Elif;
Balcı, Sibel Oğuzkan;
Çelenk, Fatih;
Kahraman, Merve;
Deniz, Murat;
Tunç, Orhan;
Durucu, Cengiz;
Mumbuç, Semih;
Kanlıkama, Muzaffer;
Pehlivan, Sacide

Publication type:

Article

THE miR-196a2T/C VARIANT AS A POSSIBLE PREDISPOSING FACTOR FOR ANKYLOSING SPONDYLITIS IN A TURKISH POPULATION.

Published in:

Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi, 2020, v. 83, n. 2, p. 81, doi. 10.26650/IUITFD.2019.0023

By:

PEHLİVAN, Sacide;
GURSOY, Savaş;
NURSAL, Ayşe Feyda;
KALTUN, Mazlum Serdar;
OZDİLLİ, Kurşat;
PEHLİVAN, Mustafa

Publication type:

Article

DNA Repair Genes and Chronic Myeloid Leukemia: ERCC2 (751), XRCC1 (399), XRCC4-Intron 3, XRCC4 (-1394) Gene Polymorphisms.

Published in:

Mediterranean Journal of Hematology & Infectious Diseases, 2021, v. 13, n. 1, p. 1, doi. 10.4084/MJHID.2021.020

By:

Ozdilli, Kursat;
Pehlivan, Mustafa;
Serin, Istemi;
Savran, Fatma Oguz;
Tomatir, Ayse Gaye;
Pehlivan, Sacide

Publication type:

Article

Is Complement Factor H Tyr402His Variant a Potential Cause of Ankylosing Spondylitis?

Published in:

Medical Bulletin of Haseki / Haseki Tip Bulteni, 2020, v. 58, n. 2, p. 142, doi. 10.4274/haseki.galenos.2020.5783

By:

Pehlivan, Sacide;
Akaltun, Mazlum Serdar;
Pehlivan, Mustafa;
Gürsoy, Savaş;
Nursal, Ayşe Feyda

Publication type:

Article

Evaluation of the macrophage migration inhibitory factor (MIF) -173 G/C variant in bipolar disorder.

Published in:

Psychiatria Danubina, 2025, v. 37, n. 1, p. 22, doi. 10.24869/psyd.2025.22

By:

Aytac, Hasan Mervan;
Yazar, Menekse Sila;
Oyaci, Yasemin;
Pehlivan, Sacide

Publication type:

Article

PERIOD3 (PER3) VNTR VARIANT ASSOCIATED WITH SEASONAL PATTERN AND FAMILY HISTORY IN BIPOLAR DISORDER.

Published in:

Psychiatria Danubina, 2022, v. 34, n. 4, p. 695, doi. 10.24869/psyd.2022.695

By:

Aytac, Hasan Mervan;
Pehlivan, Mustafa;
Oyaci, Yasemin;
Pehlivan, Sacide

Publication type:

Article

The Endothelial Nitric Oxide Synthase Gene Variants as a Risk Factor for Chronic Lymphocytic Leukemia.

Published in:

UHOD: International Journal of Hematology & Oncology / Uluslararasi Hematoloji Onkoloji Dergisi, 2017, v. 27, n. 2, p. 85, doi. 10.4999/uhod.171703

By:

PEHLIVAN, Mustafa;
TOMATIR, Ayse G.;
NURSAL, Ayşe F.;
SAHIN, Handan H.;
PEHLIVAN, Sacide

Publication type:

Article

The role of endothelial nitric oxide synthase gene polymorphisms in patients with lung cancer.

Published in:

Clinical Respiratory Journal, 2020, v. 14, n. 10, p. 948, doi. 10.1111/crj.13228

By:

Koçer, Canan;
Benlier, Necla;
Balci, Sibel Oğuzkan;
Pehlivan, Sacide;
Şanli, Maruf;
Nacak, Muradiye

Publication type:

Article

Impact of UCP2 -866G/A Variant on Smoking Risk.

Published in:

Bezmialem Science, 2021, v. 9, n. 2, p. 185, doi. 10.14235/bas.galenos.2020.4159

By:

NURSAL, Ayşe Feyda;
UYSAL, Mehmet Atilla;
PEHLİVAN, Mustafa;
SEVER, Ülgen;
PEHLİVAN, Sacide

Publication type:

Article

DNA Repair Gene (XPD, XRCC4, and XRCC1) Polymorphisms in Patients with Endometrial Hyperplasia: A Pilot Study.

Published in:

Medical Science Monitor: Basic Research, 2018, v. 24, p. 146, doi. 10.12659/MSMBR.911041

By:

Öztürk, Ebru;
Pehlivan, Sacide;
Balat, Ozcan;
Ugur, Mete Gurol;
Ozcan, Huseyin Caglayan;
Erkılıç, Suna

Publication type:

Article

A Preliminary Study of the Possible Role of Cannabinoid Receptor-1 (CNR1) Gene Polymorphisms in the Development of Morbid Obesity in Obese Children.

Published in:

2015

By:

Araz, Nilgün Çöl;
Nacak, Muradiye;
Balcı, Sibel Oğuzkan;
Pehlivan, Sacide;
Balat, Ayşe

Publication type:

Abstract

The Possible Role of Mitochondrial Uncoupling Protein 2 (UCP2) Gene on the Development of Metabolic Syndrome and Platelet Count in Obese Children/Adolescents - A Preliminary Study.

Published in:

2015

By:

Araz, Nilgün Çöl;
Balcı, Sibel Oğuzkan;
Nacak, Muradiye;
Balat, Ayşe;
Pehlivan, Sacide

Publication type:

Abstract

A Preliminary Study of the Possible Role of Cannabinoid Receptor-1 (CNR1) Gene Polymorphisms in the Development of Morbid Obesity in Obese Children.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 87

By:

Araz, Nilgün Çöl;
Nacak, Muradiye;
Balcı, Sibel Oğuzkan;
Pehlivan, Sacide;
Balat, Ayşe

Publication type:

Article

The Possible Role of Mitochondrial Uncoupling Protein 2 (UCP2) Gene on the Development of Metabolic Syndrome and Platelet Count in Obese Children/Adolescents - A Preliminary Study.

Published in:

Journal of Clinical Research in Pediatric Endocrinology, 2015, v. 7, p. 66

By:

Araz, Nilgün Çöl;
Balcı, Sibel Oğuzkan;
Nacak, Muradiye;
Balat, Ayşe;
Pehlivan, Sacide

Publication type:

Article