نتایج جستجو برای: healthy carrier

تعداد نتایج: 348342  

2016
Shahnaz Sali Soheil Tavakolpour Baharan Farkhondemehr

Background and Aims: During recent years, the relationship between vitamin D levels and chronic hepatitis B (CHB) infection has attracted many researchers' attention. However, the results relating to the association of vitamin D levels and HBV infection have been conflicting and there remains a lack of knowledge about the effects of antiviral treatments on vitamin D level. Methods: Eighty-four ...

Journal: :acta medica iranica 0
fardeen ali malayeri department of neurogenetics, iranian center of neurological research, imam khomeini hospital , tehran university of medical sciences, tehran, iran. and department of clinical biochemistry, isfahan pharmaceutical sciences research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical sciences, isfahan, iran. mojtaba panjehpour department of clinical biochemistry, isfahan pharmaceutical sciences research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical sciences, isfahan, iran. ahmad movahedian department of clinical biochemistry, isfahan pharmaceutical sciences research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical sciences, isfahan, iran. majid ghaffarpour iranian center of neurological research, imam khomeini hospital, tehran university of medical sciences, tehran, iran. gholam reza zamani department of neurology, children medical center, school of medicine, tehran university of medical sciences, tehran, iran. hajifaraj tabrizi department of medical genetics, school of medicine, tehran university of medical sciences, tehran, iran.

this study determines the value of linkage analysis using six rflp markers for carrier detection and prenatal diagnosis in familial dmd/bmd cases and their family members for the first time in the iranian population. we studied the dystrophin gene in 33 unrelated patients with clinical diagnosis of dmd or bmd. subsequently, we determined the rate of heterozygosity for six intragenic rflp marker...

Journal: :Journal of controlled release : official journal of the Controlled Release Society 2011
Andres J Calderon Tridib Bhowmick John Leferovich Bharat Burman Benjamin Pichette Vladimir Muzykantov David M Eckmann Silvia Muro

Targeting of drug carriers to cell adhesion molecules expressed on endothelial cells (ECs) may improve treatment of diseases involving the vascular endothelium. This is the case for carriers targeted to intercellular adhesion molecule 1 (ICAM-1), an endothelial surface protein overexpressed in many pathologies. In order to optimize our design of anti-ICAM carriers, we have explored in this stud...

Journal: :European cytokine network 2006
Ilona Bányász Géza Bokodi Barna Vásárhelyi András Treszl László Derzbach András Szabó Tivadar Tulassay Adám Vannay

Low birth weight (LBW) infants have increased susceptibility to perinatal complications. An immature and impaired vascular system may possibly participate in these complications. There is evidence that supports the notion that vascular endothelial growth factor (VEGF), which is an essential regulator of embryonic angiogenesis, plays a central role in the pathogenesis of perinatal complications....

2017
Malinee Pongsavee Kamol Wisuwan Danai Tiwawech

Background: Breast cancer is a major public health problem around the world, including Thailand and it has the highest ranking among female cancer. Currently, the diversity or polymorphism of ERCC1 gene (excision repair cross-complementary group 1 gene or ERCC1) was reported to associate with an increased risk of breast cancer. This study aims to investigate the relationship between ERCC1 polym...

2002
Paola Marchisio Susanna Esposito Gian Carlo Schito Anna Marchese Roberta Cavagna Nicola Principi

We assessed the prevalence of Streptococcus pneumoniae serotypes in the nasopharynx of healthy children, antimicrobial susceptibility patterns, risk factors for carriage, and the coverage of heptavalent pneumococcal conjugate vaccine. In 2,799 healthy infants and children, the S. pneumoniae carrier rate was 8.6% (serotypes 3, 19F, 23F, 19A, 6B, and 14 were most common). Most pneumococci (69.4%)...

2010
Gunjan Joshi Sunil Pradhan Balraj Mittal

We aimed to find out if the serotonin receptor (HT102T>C) and serotonin transporter (STin 2) polymorphisms play any role in genetic susceptibility of migraine. For the study, 217 migraine patients and 217 healthy controls (HC) were recruited and genotyping was carried out using the Polymerase Chain Reaction and Restriction Fragment Length polymorphism (PCR-RFLP) method. All results were Bonferr...

2013
Julia Vodopiutz Heinz Zoller Aimée L. Fenwick Richard Arnhold Max Schmid Daniela Prayer Thomas Müller Andreas Repa Arnold Pollak Christoph Aufricht Andrew O.M. Wilkie Andreas R. Janecke

OBJECTIVE To delineate a novel autosomal recessive multiple congenital anomaly-mental retardation (MCA-MR) syndrome in 2 female siblings of a consanguineous pedigree and to identify the disease-causing mutation. STUDY DESIGN Both siblings were clinically characterized and homozygosity mapping and sequencing of candidate genes were applied. The contribution of nonsense-mediated messenger RNA (...

Journal: :Turkish journal of medical sciences 2014
Yiiksel Maraş Ali Akdoğan Bünyamin Kisacik Levent Kiliç Engin Yilmaz Abdurrahman Tufan Umut Kalyoncu Şaziye Şule Apraş Bilgen Sedat Kiraz Ali İhsan Ertenli Meral Çalgüneri

BACKGROUND/AIM To define the frequency of familial Mediterranean fever gene (MEFV) mutations in ankylosing spondylitis (AS) and describe different clinical aspects of MEFV mutation carrier and noncarrier AS patients. MATERIALS AND METHODS In 112 AS patients, Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and Bath Ankylosing Spondylitis Functional Index (BASFI) scores were calcula...

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