نتایج جستجو برای: specific phenotype

تعداد نتایج: 1163345  

Journal: :iranian journal of basic medical sciences 0
ghasem mosayebi molecular and medicine research center, school of medicine, arak university of medical sciences, arak, iran sayyed mohammad moazzeni department of immunology, school of medical sciences, tarbiat modarres university, tehran, iran

introduction dendritic cells (dcs) are bone marrow-derived cells, which migrate to lymphoid and non-lymphoid organs via blood. liver dcs are believed to play an important role in the regulation of hepatic allograft acceptance. however, because of inherent difficulties in isolating adequate numbers of dcs from liver, limited information is available on the phenotype and functions of liver dcs. t...

Journal: :world journal of plastic surgery 0
madhumita gupta department of plastic and reconstructive surgery, ipgme & r, kolkata, india ashwin alke pai department of plastic and reconstructive surgery, ipgme & r, kolkata, india abhimanyu bhattacharya department of plastic and reconstructive surgery, ipgme & r, kolkata, india ravi ramachandra department of plastic and reconstructive surgery, ipgme & r, kolkata, india raghavendra sawarappa department of plastic and reconstructive surgery, ipgme & r, kolkata, india subhakanta mohapatra department of plastic and reconstructive surgery, ipgme & r, kolkata, india

apert syndrome is a congenital craniosynostosis syndrome comprising of bilateral coronal synostosis , symmetric syndactyly of hands and feet and midface hypoplasia. we present an atypical phenotype of this syndrome with right sided unilateral coronal synostosis. however, type i apert hand and other clinical and radiological features suggestthe diagnosis. genetic analysis revealed an absence of ...

ژورنال: Medical Laboratory Journal 2011
Jafarpur M, , Mirzaee A, , Nazemi A, , Rahbar Farzamee hagh S, ,

Abstract Background and objectives: Group A Streptococcus (GAS) strains have been identified by serologic methods based on surface protein antigens, T and M. Accordingly, different serotypes have been reported worldwide. Recently, the previous out of date procedures have been replaced by N-terminal emm gene sequence, which has been used in identifying more than 150 emm types. We aimed to determ...

Journal: :مجله بین المللی زیست و زیست پزشکی 0
mohammad reza esmaeili dooki non-communicable pediatric diseases research center, babol university of medical sciences, babol, iran haleh akhavan-niaki genetic laboratory of amirkola children’s hospital, babol university of medical sciences, babol, iran soraya shabani genetic laboratory of amirkola children’s hospital, babol university of medical sciences, babol, iran reza tabaripour department of cellular and molecular biology, islamic azad university, babol-branch, iran

cystic fibrosis is an autosomal recessive disease caused by a wide spectrum of mutations in the gene encoding for the cystic fibrosis transmembrane conductance regulator protein. these mutations that correlate with different phenotypes, vary in their frequency and distribution in different populations. in this study missense mutation r117h that associated with the different clinical symptoms wa...

Journal: :caspian journal of internal medicine 0
shiran mohammad reza fatemeh sarzare fatemeh merat ebrahim salehifar ali akbar moghadamnia seyed mohammad bagher hashemi soteh

background: cyp2d6 is polymorphically expressed enzyme that show marked interindividual and interethnic variation. phenotyping of cyp2d6 provides valuable information about real-time activity of this important drug-metabolizing enzymes through the use of specific probe drugs. the aim of this study was to identify the cyp2d6 oxidation phenotype with dextromethorphan (dex) as a probe drug in maza...

ژورنال: دانشور پزشکی 2020
Ahmadi, Fatemeh , Alebouyeh, Masoud , Besharati, Saeed , Eslami, Parisa , Fani, Fereshteh , Farzami, Marjan Rahnamaye , Ganji, Leila , Majidpour, Ali , Moghadam, Somayeh Soleymanzadeh , MohammadSalehi, Reza , Nikmanesh, Bahram , Owlia, Parviz , Pouladfar, Gholamreza , Sadeghi, Atena , Tajeddin, Elahe ,

Background and Objective: Pathogenic species of Campylobacter, in addition to diarrhea and gastrointestinal diseases, could cause debilitating auto-immune and chronic diseases in humans. Investigation of the existence of this bacterium in food sources and clinical samples, and detection of antibiotic resistance could be helpful in the control of its spread and treatment procedures. The aim of t...

Constanze Csaki Ebrahim Esfandiary, Farahnaz Moulavi Fariba Moulavi Khalilollah Nazem Masoud Hatef Dehghani Mehdi Shakibaei Mehrafarin Fesharaki Mohammad Hossein Nasr-esfahani Noshin Amirpour Shahnaz Razavi,

Objective(s) Articular cartilage tissue defects cannot be repaired by the proliferation of resident chondrocytes. Autologous chondrocyte transplantation (ACT) is a relatively new therapeutic approach to cover full thickness articular cartilage defects by in vitro grown chondrocytes from the joint of a patient. Therefore, we investigated the redifferentiation capability of human chondrocytes ma...

Journal: :iranian journal of veterinary research 2014
s. roushan zadeh m. h. eskandari s. s. shekarforoush a. hosseini

morphological, biochemical and molecular characteristics were studied to identify dominant lactic acid bacteria (lab), isolated from traditional yoghurts produced by tribes of iran. from 60 yoghurt samples, a total of 137 lab isolates were determined, in which 66 and 71 were identified as lactic acid cocci and bacilli, respectively. biochemical tests showed the occurrence of 9.76% mesophilic ho...

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