نتایج جستجو برای: genotype d

تعداد نتایج: 663177  

Journal: :Cardiovascular Diabetology 2009
Joey C Eisenmann Mark A Sarzynski Kim Glenn Max Rothschild Kate A Heelan

BACKGROUND Angiotensin converting enzyme (ACE) is a possible candidate gene that may influence both body fatness and blood pressure. Although several genetic studies have been conducted in adults, relatively few studies have examined the contribution of potential candidate genes, and specifically ACE I/D, on adiposity and BP phenotypes in childhood. Such studies may prove insightful for the dev...

Journal: :Journal of clinical microbiology 1999
S Bertout F Renaud D Swinne M Mallié J M Bastide

The genotypes of 107 strains of Cryptococcus isolated from the environment or from patients from various geographical areas were determined by multilocus enzyme electrophoresis (MLEE). We analyzed the relationships between genotype structure and serotype and between genotype structure and strain origin. Twelve of the 14 enzyme-encoding loci studied were polymorphic, giving rise to 48 electropho...

Journal: :Diabetes 2005
Laurent Weekers Béatrice Bouhanick Samy Hadjadj Yves Gallois Ronen Roussel Franck Pean Amos Ankotche Gilles Chatellier François Alhenc-Gelas Pierre J Lefebvre Michel Marre

ACE inhibition protects kidney function, but ACE insertion/deletion (I/D) polymorphism affects renal prognosis in type 1 diabetic patients. ACE genotype may influence the renal benefits of ACE inhibition. We studied the impact of ACE I/D polymorphism on the renal hemodynamic changes induced by ACE inhibition in type 1 diabetes. We studied renal hemodynamics (glomerular filtration rate [GFR], ef...

2017
Kessarin Thanapirom Sirinporn Suksawatamnuay Wattana Sukeepaisarnjaroen Pisit Tangkijvanich Sombat Treeprasertsuk Panarat Thaimai Rujipat Wasitthankasem Yong Poovorawan Piyawat Komolmit

BACKGROUND Patients with chronic hepatitis C (HCV) infection have high prevalence of vitamin D deficiency. Genome-wide association study data has showed that several genetic variants within vitamin D cascade affect vitamin D function. This study aimed to determine whether genetic polymorphisms of genes in the vitamin D pathway are associated with treatment responses to pegylated interferon (PEG...

2009
Priscila A Tonetto Neiva SL Gonçales Viviane C Fais Aline G Vigani Eduardo SL Gonçales Adriana Feltrin Fernando L Gonçales

BACKGROUND Knowledge of HBV genotype is very important for clinical treatment. Studies have suggested possible pathogenic and therapeutic differences among HBV genotypes. The aim of this study was to determine HBV subtypes and genotypes in HBV-infected patients in our region (southeast Brazil) and to correlate results with clinical and histopathological data. METHODS One hundred and thirty-ni...

2014
Mayumi Imahashi Taisuke Izumi Dai Watanabe Junji Imamura Kazuhiro Matsuoka Hirotaka Ode Takashi Masaoka Kei Sato Noriyo Kaneko Seiichi Ichikawa Yoshio Koyanagi Akifumi Takaori-Kondo Makoto Utsumi Yoshiyuki Yokomaku Takuma Shirasaka Wataru Sugiura Yasumasa Iwatani Tomoki Naoe

OBJECTIVE The human APOBEC3 family of proteins potently restricts HIV-1 replication APOBEC3B, one of the family genes, is frequently deleted in human populations. Two previous studies reached inconsistent conclusions regarding the effects of APOBEC3B loss on HIV-1 acquisition and pathogenesis. Therefore, it was necessary to verify the effects of APOBEC3B on HIV-1 infection in vivo. METHODS In...

Journal: :The Tohoku journal of experimental medicine 2007
Duygu Gezen-Ak Erdinç Dursun Turan Ertan Haşmet Hanağasi Hakan Gürvit Murat Emre Engin Eker Melek Oztürk Funda Engin Selma Yilmazer

Vitamin D(3) is known to be involved in neuroprotection and exert its neuroprotective effects by modulating neuronal calcium homeostasis and production of neurotrophins. The single nucleotide polymorphisms (SNP) in vitamin D receptor (VDR) gene which can influence the affinity of vitamin D(3) to its receptor may be related to neurodegenerative diseases and neuronal damage by altering the vitami...

Journal: :Genetics and molecular research : GMR 2013
A I Guney D Ergec D Kirac H Ozturhan M Caner G Koc C Kaspar K Ulucan M Agirbasli

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 obesity. Also polymorphisms in the angiotensin-I converting enzyme (ACE) gene can associate with CAD. The relationship between ACE polymorphisms and other risk factors is not well understood in CAD, lik...

2013
Sinem Nalbantoglu Yılmaz Tabel Sevgi Mir Erkin Serdaroğlu Afig Berdeli

Henoch-Schönlein purpura (HSP) is a small-vessel vasculitis of autoimmune hypersensitivity, and renin-angiotensin system (RAS) regulates vascular homeostasis and inflammation with activation of cytokine release. Thus, we aimed to investigate the association between HSP and ACE I/D and AGT M235T polymorphisms. Genotyping was determined by allele specific PCR and PCR-RFLP. We obtained a significa...

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