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Nilüfer Bozkurt

Research Profile

Geographic Areas

Turkey

Physiology

Concepts & Ideas

Genes & Molecular Sequences

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Procedures

Chemicals & Drugs

Disorders

Behcet's Syndrome

Anatomy

Retina

Co-author Network

Publications

TOP 3
Firdevs Baş; Merih Berberoğlu; Abdullah Bereket; Aysun Bideci; Ece Böber; Nilüfer Bozkurt; M Emre Atabek; Zehra Aycan; Peyami Cinaz; Feyza Darendeliler; Korcan Demir; Damla Gökşen Şimşek; Turgay Isbir; Sema Kabataş Eryılmaz; Banu Küçükemre Aydın; Zeynep Sıklar; Serap Turan; Filiz Tütüncüler; Ozan Uzunhan; Ergun Cetinkaya; Semra Çetinkaya; Sukran Darcan; Gönül Ocal; Özlem Timirci; Rüveyde Bundak
The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study.
Firdevs Baş; Nilüfer Bozkurt; Rüveyde Bundak; Turgay Isbir; Sema Kabataş Eryılmaz; Fatih Keleşoğlu; Banu Küçükemre Aydın; Özlem Timirci; Feyza Darendeliler
The distribution of exon 3-deleted/full-length growth hormone receptor polymorphism in the Turkish population.
Nilüfer Bozkurt; A Başgül Yigiter; Husnu Gokaslan; Zehra Nese Kavak
Correlations of fetal-maternal outcomes and first trimester 3-D placental volume/3-D power Doppler calculations.

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All Publications

2012: Firdevs Baş; Merih Berberoğlu; Abdullah Bereket; Aysun Bideci; Ece Böber; Nilüfer Bozkurt; M Emre Atabek; Zehra Aycan; Peyami Cinaz; Feyza Darendeliler; Korcan Demir; Damla Gökşen Şimşek; Turgay Isbir; Sema Kabataş Eryılmaz; Banu Küçükemre Aydın; Zeynep Sıklar; Serap Turan; Filiz Tütüncüler; Ozan Uzunhan; Ergun Cetinkaya; Semra Çetinkaya; Sukran Darcan; Gönül Ocal; Özlem Timirci; Rüveyde Bundak
The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study.
Hormone research in pædiatrics 2012;77(2):85-93.
2011: Firdevs Baş; Nilüfer Bozkurt; Rüveyde Bundak; Turgay Isbir; Sema Kabataş Eryılmaz; Fatih Keleşoğlu; Banu Küçükemre Aydın; Özlem Timirci; Feyza Darendeliler
The distribution of exon 3-deleted/full-length growth hormone receptor polymorphism in the Turkish population.
Journal of clinical research in pediatric endocrinology 2011;3(3):126-31.
2010: Nilüfer Bozkurt; A Başgül Yigiter; Husnu Gokaslan; Zehra Nese Kavak
Correlations of fetal-maternal outcomes and first trimester 3-D placental volume/3-D power Doppler calculations.
Clinical and experimental obstetrics & gynecology 2010;37(1):26-8.
2008: Atike Tekeli; Selim Isbir; Arzu Ergen; Uzay Görmüş; Nilüfer Bozkurt; Ozlem Timirci; Sinan Arsan; TURGAY ISBIR
APE1 and XRCC3 polymorphisms and myocardial infarction.
In vivo (Athens, Greece) 2008;22(4):477-9.
2008: I Yaylim-Eraltan; Nilüfer Bozkurt; A Ergen; Umit Zeybek; O Ozturk; Soykan Arikan; Yesim Erbil; Ilhami Uslu; Hakan Camlica; TURGAY ISBIR
L-myc gene polymorphism and risk of thyroid cancer.
Experimental oncology 2008;30(2):117-20.
2007: Uzay Gormus; Arzu Ergen; Ilhan Yaylim-Eraltan; Hulya Yilmaz; Akif Turna; Nilüfer Bozkurt; TURGAY ISBIR
Fas-1377 A/G polymorphism in lung cancer.
In vivo (Athens, Greece) 2007;21(4):663-6.
2007: Bulent Yigit; Nilüfer Bozkurt; Ibrahim Berber; Izzet Titiz; TURGAY ISBIR
Analysis of CC chemokine receptor 5 and 2 polymorphisms and renal transplant survival.
Cell biochemistry and function 2007;25(4):423-6.
2007: Bulent Yigit; Nilüfer Bozkurt; Fehmi Narter; Hulya Yilmaz; Ergin Yucebas; TURGAY ISBIR
Effects of ACE I/D polymorphism on prostate cancer risk, tumor grade and metastatis.
Anticancer research 2007;27(2):933-6.
2007: Alin Basgül; A Uzuner; Zehra Nese Kavak; Nilüfer Bozkurt; H Onaran; M S Ertürk
Impact of tubal sterilization on women's health.
Clinical and experimental obstetrics & gynecology 2007;34(1):39-41.
2006: Bulent Yigit; Nilüfer Bozkurt; Ilhan Yaylim; Izzet Titiz; TURGAY ISBIR
Analysis of L-myc gene polymorphism in patients with renal failure outcome to renal transplant.
Transplantation proceedings 2006;38(5):1267-9.
2006: Ali Metin Kafadar; Hulya Yilmaz; Didem Kafadar; Arzu Ergen; Umit Zeybek; Nilüfer Bozkurt; Cengiz Kuday; TURGAY ISBIR
C677T gene polymorphism of methylenetetrahydrofolate reductase (MTHFR) in meningiomas and high-grade gliomas.
Anticancer research 2006;26(3B):2445-9.
2006: Nese Karaaslan Biyikli; Harika Alpay; Nurdan Yildiz; Bedia Agachan; Arzu Ergen; Umit Zeybek; Nilüfer Bozkurt; Turgay Ispir
Paraoxonase 1 192 and 55 polymorphisms in nephrotic children.
Pediatric nephrology (Berlin, Germany) 2006;21(5):649-54.
2006: Alin Basgul; Husnu Gokaslan; Zehra Nese Kavak; Funda Eren; Nilüfer Bozkurt
Primary yolk sac tumor (endodermal sinus tumor) of the vulva: case report and review of the literature.
European journal of gynaecological oncology 2006;27(4):395-8.
2003: Ilhan Yaylim; Nilüfer Bozkurt; Hulya Yilmaz; TURGAY ISBIR; Nilgün Isik; Soykan Arikan
The apolipoprotein E epsilon 4 allele is not a risk factor for Turkish breast cancer patients.
Cancer genetics and cytogenetics 2003;146(1):86-7.
2003: Nilüfer Bozkurt; Haluk Kazokoglu; Sule Yavuz; Tayfun Bavbek; Haner Direskeneli
Elevated serum chemokine levels in Behçet's disease with uveitis.
Rheumatology international 2003;23(5):268-9.
2001: Nilüfer Bozkurt; O Oztürk; TURGAY ISBIR
New MCAD gene mutation, not previously reported in other nations, found at A1161G in Turkish population.
American journal of medical genetics 2001;103(3):255-6.
2000: Zeynep Eti; A Yayci; Tümay Umuroglu; F Y Gögüş; Nilüfer Bozkurt
The effect of propofol and alfentanil on the increase in intraocular pressure due to succinylcholine and intubation.
European journal of ophthalmology 2000;10(2):105-9.
2000: S Kurhan-Yavuz; Haner Direskeneli; Nilüfer Bozkurt; Yilmaz Ozyazgan; Tayfun Bavbek; Haluk Kazokoglu; Emel Eksioglu-Demiralp; Gerhild Wildner; Maria Diedrichs-Möhring; T Akoglu
Anti-MHC autoimmunity in Behçet's disease: T cell responses to an HLA-B-derived peptide cross-reactive with retinal-S antigen in patients with uveitis.
Clinical and experimental immunology 2000;120(1):162-6.
1998: Nilüfer Bozkurt; Tayfun Bavbek; H Kazokoğlu
Hereditary pigmented paravenous chorioretinal atrophy.
Ophthalmic genetics 1998;19(2):99-104.