Nasal pepsin assay and pH monitoring in chronic rhinosinusitis
S Ozmen, OT Yücel, I Sinici, OA Ozmen… - The …, 2008 - Wiley Online Library
Objectives/Hypothesis: The primary objective of this study was to determine the relationship
between chronic rhinosinusitis (CRS) and laryngopharyngeal reflux (LPR). We also …
between chronic rhinosinusitis (CRS) and laryngopharyngeal reflux (LPR). We also …
Why are they having infant colic? A nested case–control study
…, E Örün, B Mutlu, Y Madendağ, I Sinici… - Paediatric and …, 2010 - Wiley Online Library
Yalçın SS, Örün E, Mutlu B, Madendağ Y, Sinici İ, Dursun A, Özkara HA, Üstünyurt Z, Kutluk
Ş, Yurdakök K. Why are they having infant colic? A nested case–control study. Paediatric …
Ş, Yurdakök K. Why are they having infant colic? A nested case–control study. Paediatric …
T-786C polymorphism in promoter of eNOS gene as genetic risk factor in patients with erectile dysfunction in Turkish population
İ Sinici, EO Güven, E Şerefoğlu, M Hayran - Urology, 2010 - Elsevier
OBJECTIVES: To investigate the effect of 2 endothelial nitric oxide synthase gene
polymorphisms, namely, variable number of 27-bp tandem repeats in intron 4 and T-786C in the …
polymorphisms, namely, variable number of 27-bp tandem repeats in intron 4 and T-786C in the …
Protective role of 27bp repeat polymorphism in intron 4 of eNOS gene in lacunar infarction
M Yemişçi, M Yemişçi, I Sinici, HA Özkara… - Free radical …, 2009 - Taylor & Francis
Association of the three potential endothelial nitric oxide synthase gene (eNOS) polymorphisms
(T-786C in promoter region, G894T in exon 7 and tandem 27-bp repeats in intron 4) with …
(T-786C in promoter region, G894T in exon 7 and tandem 27-bp repeats in intron 4) with …
Effects of hormone replacement therapy on plasma homocysteine and C-reactive protein levels
…, H Yarali, G Kabakci, O Bukulmez, I Sinici… - Gynecologic and …, 2002 - karger.com
In order to investigate the effect of hormone replacement therapy (HRT) on plasma
homocysteine and C-reactive protein (CRP) levels 46 healthy postmenopausal women were …
homocysteine and C-reactive protein (CRP) levels 46 healthy postmenopausal women were …
[HTML][HTML] In cellulo examination of a beta-alpha hybrid construct of beta-hexosaminidase A subunits, reported to interact with the GM2 activator protein and hydrolyze …
I Sinici, S Yonekawa, I Tkachyova, SJ Gray… - PLoS …, 2013 - journals.plos.org
The hydrolysis in lysosomes of GM2 ganglioside to GM3 ganglioside requires the correct
synthesis, intracellular assembly and transport of three separate gene products; ie, the alpha …
synthesis, intracellular assembly and transport of three separate gene products; ie, the alpha …
Extent of coronary atherosclerosis and homocysteine affect endothelial markers
A Yildirir, SL Tokgozoglu, I Haznedaroglu, I Sinici… - …, 2001 - journals.sagepub.com
The aim of the study was to evaluate the effects of the presence, extent, and clinical stability
of coronary artery disease on endothelial function parameters, C-reactive protein and homo …
of coronary artery disease on endothelial function parameters, C-reactive protein and homo …
Intron 4 VNTR polymorphism of eNOS gene is protective for cardiac syndrome X
Microvascular abnormalities caused by endothelial dysfunction seem to be responsible for
the myocardial ischemia in patients with cardiac syndrome X (CSX). Nitric oxide is a key …
the myocardial ischemia in patients with cardiac syndrome X (CSX). Nitric oxide is a key …
Comparison of HCMV IE and EF-1 promoters for the stable expression of β-subunit of hexosaminidase in CHO cell lines
I Sinici, M Zarghooni, MB Tropak, DJ Mahuran… - Biochemical …, 2006 - Springer
The ability to use in vitro mutagenesis and transfection techniques to generate stable cell
lines that highly express a mutant protein associated with a metabolic disease has been an …
lines that highly express a mutant protein associated with a metabolic disease has been an …
Identification of two novel arylsulfatase A mutations with a polymorphism as a cause of metachromatic leukodystrophy
E Oender, I Sinici, FM Sönmez, M Topçu… - Neurological …, 2009 - Taylor & Francis
Objective: Metachromatic leukodystrophy is a lysosomal storage disorder caused by the
deficiency of arylsulfatase A or saposin B. Enzyme deficiency leads to the accumulation of …
deficiency of arylsulfatase A or saposin B. Enzyme deficiency leads to the accumulation of …