نتایج جستجو برای: x gene

تعداد نتایج: 1708133  

Journal: :iranian red crescent medical journal 0
hamid alavi majd department of biostatistics, school of paramedical sciences, shahid beheshti university of medical sciences, tehran, ir iran atefeh talebi department of biostatistics, school of paramedial sciences, students’ research committee, shahid beheshti university of medical sciences, tehran, ir iran; department of biostatistics, school of paramedial sciences, students’ research committee, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-2122707347, fax: +98-2122721150 kambiz gilany reproductive biotechnology research center, avicenna research institute, acecr, tehran, ir iran nasibeh khayyer proteomics research center, shahid beheshti university of medical sciences, tehran, ir iran

conclusions some results of the correlation coefficients are not the same with visualization. the reason may be due to the small number of data. materials and methods in the foundation-application study, we constructed two-way gene networks using nonparametric methods, such as spearman’s rank correlation coefficient and blomqvist’s measure, and compared them with pearson’s correlation coefficie...

2013
Xinhua Shu

Copyright: © 2013 Shu X. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Retinitis Pigmentosa (RP) is a group of heterogeneous genetic disorders with a worldwide prevalence of 1 in 4000 individuals [1]. RP can...

A. Zahedmehr, M. Lak R. Sharifian S. Delmaghani S. Zeinali

Background: Hemophilia B is an X-linked recessive coagulation disorder caused by factor IX deficiency.  Analysis of factor IX gene polymorphisms is considered the best approach for prenatal diagnosis and carrier detection of hemophilia B where the identification of gene mutation is not easily possible. Objective: To study the frequency of three factor IX-linked restriction fragment length polym...

Backgrounds: Hypohidrotic ectodermal dysplasia (HED) is a rare genetic disorder, distinguished by hypotrichosis, hypohidrosis, and hypodontia. HDE can be inherited in X-linked recessive manner as a result of mutations in the ectodysplasin A (EDA) gene as well as autosomal dominant and autosomal recessive manners both of them caused by mutations in EDA receptor (EDAR) and EDAR-associated death d...

To overcome the problems of gene and drug delivery, nanotechnology has gained interest in recent years. Nanosystems with different compositions and biological properties have been extensively investigated for drug and gene delivery applications. Nanotechnology in drug delivery has been manifested into nanoparticles that can have unique properties both in vitro and in vivo, especially in targete...

Journal: :iranian journal of immunology 0
masoumeh rajabibazl department of clinical biochemistry, faculty of medicine, shahid beheshti university of medical sciences mohammad javad rasaee department of medical biotechnology, faculty of medical sciences, tarbiat modares university, tehran, iran mehdi forouzandeh department of medical biotechnology, faculty of medical sciences, tarbiat modares university, tehran, iran azam rahimpour department of medical biotechnology, faculty of medical sciences, tarbiat modares university, tehran, iran

background: single domain antibodies from camel heavy chain antibodies (vhh or nanobody), are advantages due to higher solubility, stability, high homology with human antibody, lower immunogenicity and low molecular weight. these criteria make them candidates for production of engineered antibody fragments particularly in transgenic animals. objective: to study the development of transgenic chi...

ژورنال: پژوهشنامه تربیتی 2005
حسن احدی حسن توزنده جانی حسین آزاد علی دلاور

این پژوهش از نوع پژوهشهایی تجربی و مبتنی بر نظریه های شـناختی ـ رفتـاریو زیست شیمیایی درمان اختلالهای روانی و به منظور ارزیابی کار آمـدی نسـبی تکنیـکهای شناختی ـ رفتاری، دارو درمانی و ترک یـب آنهـا در درمـان اخـتلال وسـواس فکـریوعملی انجام شده است. بدین منظور ما از بین مراجعین زن و مرد (متأهل و مجرد ،51 تا 54 ساله) مراجعه کننده به کلینیکهای روانشناسی ،4 گروه 8 نفری بـه صـورت تصـادفیجایگزینی انت...

Background The X-linked cyclin-dependent kinase like 5 (CDKL5/STK9) gene has been shown to be responsible for a severe encephalopathy condition characterized by early onset of epilepsy and severe developmental delay. CDKL5 mutations have been shown to be more frequent among female patients. Results Here we report a 6- month male patient, second child of a healthy non consanguineous in the Irani...

Introduction: The therapeutic properties of Olibanum have been considered in traditional medicine since ages past. Recent studies indicated the effect of Olibanum on memory enhancement and prevention/treatment of Alzheimer's disease. Fragile X mental retardation protein is the product of the FMR1 gene that mediates memory formation through the development of communications between nerve cells. ...

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