نتایج جستجو برای: heteroduplex analysis

تعداد نتایج: 2824796  

Journal: :iranian journal of immunology 0
natarajan sudhakar dept of molecular oncology nirmala karunakaran nancy dept of molecular oncology kamalalayam raghavan rajalekshmy dept of hematology and immunology, cancer institute (wia), 38, sardar patel road, chennai 600036 thangarajan rajkumar dept of molecular oncology

background: precursor b-acute lymphoblastic leukemia (precursor b-all) oc-curs due to the uncontrolled proliferation of b-lymphoid precursors arrested at a par-ticular stage of b-cell development. precursor-b-all is classified mainly into pro-b-all, common-all and pre-b-all. the common acute lymphoblastic antigen cd10 is the marker for common-all. objective: this study was aimed to examine the ...

Journal: :Clinical Chemistry 2007

ژورنال: :مجله دانشگاه علوم پزشکی شهرکرد 0
مریم طاهرزاده قهفرخی mryam tahrzadehgharofi عفت فرخی efat farkhoi سید ابوالفتح شیرمردی seyed abolfateh shirmardi جواد صفاری چالشتری javad safari chaleshtori سمیه اسدی somayeh asadi کیهان قطره سامانی keyhan ghatreh samani مرضیه ابوالحسنی

زمینه و هدف: وقوع ناشنوایی پیش زبانی حدود 1 در 1000 تولد است که بیش از 60% موارد آن ارثی هستند. ناشنوایی اختلالی هتروژن محسوب می شود و ممکن است به علل محیطی، ژنتیکی یا هر دو رخ دهد. اخیراً جهش های ژن dfnb59 که رمز کننده پروتئین پژواکین است به عنوان عامل ناشنوایی نوع عصبی معرفی شده اند. این مطالعه با هدف بررسی نوع و فراوانی جهش های ژن dfnb59 در 100 ناشنوای غیرسندرومی، در استان چهارمحال و بختیاری ...

Journal: :Methods in molecular medicine 2002
Julian Zielenski Isabel Aznarez Tuncer Onay John Tzounzouris Danuta Markiewicz Lap-Chee Tsui

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه پیام نور - دانشگاه پیام نور استان تهران - دانشکده علوم پایه 1388

چکیده: مقدمه: هایپرکلسترولمی فامیلی (fh) بیماری غالب اتوزومال است و با افزایش سطح لیپوپروتئین با دانسیته کم (در پلاسما) ، لیپید در تاندون و رگها تجمع می یابد. این بیماری با آترواسکلروز نابهنگام و افزایش خطر بیماری های قلبی عروقی (chd ) همراه می شود. هایپرکلسترولمیای فامیلی به همراه جهش در ژن گیرنده لیپوپروتئین با دانسیته کم (ldlr ) ایجاد می شود. از اهداف این مطالعه بررسی تغییرات ژن ldlr در گرو...

Journal: :Journal of clinical microbiology 2009
Christina O Igboin Ann L Griffen Eugene J Leys

Porphyromonas gingivalis is implicated in the etiology of chronic periodontitis. Genotyping studies suggest that genetic variability exists among P. gingivalis strains; however, the extent of variability remains unclear and regions of variability remain largely unidentified. To assess P. gingivalis strain diversity, we previously used heteroduplex analysis of the ribosomal operon intergenic spa...

Journal: :Haematologica 1999
Y González R Martino N Rabella R Labeaga I Badell J Sierra

BACKGROUND AND OBJECTIVE The main difficulty of PCR-based clonality studies for B-cell lymphoproliferative disorders (B-LPD) is discrimination between monoclonal and polyclonal PCR products, especially when there is a high background of polyclonal B cells in the tumor sample. Actually, PCR-based methods for clonality assessment require additional analysis of the PCR products in order to discern...

Journal: :iranian red crescent medical journal 0
negar moradipour cellular and molecular research center, shahrekord university of medical sciences, shahrekord, ir iran payam ghasemi-dehkordi cellular and molecular research center, shahrekord university of medical sciences, shahrekord, ir iran fatemeh heibati clinical biochemistry research center, shahrekord university of medical sciences, sharekord, ir iran shahrbanuo parchami-barjui cellular and molecular research center, shahrekord university of medical sciences, shahrekord, ir iran marziyeh abolhasani cellular and molecular research center, shahrekord university of medical sciences, shahrekord, ir iran ahmad rashki department of physiopathology, faculty of veterinary medicine, zabol university, zabol, ir iran

conclusions more studies are needed to investigate the relationship between other parts of this gene with hearing loss in different populations through the country. more research could clarify the role of this gene and its relation with deafness and provide essential information for the prevention and management of auditory disorders caused by genetic factors in the iranian population. backgrou...

Journal: :Clinical chemistry 1997
B G Henderson P R Wenham J P Ashby G Blundell

Familial defective apolipoprotein (apo) B-100 (FDB), a condition that may give rise to hypercholesterolemia, is caused by mutations around codon 3500 of the apo B gene. We have compared the ability of three molecular-scanning techniques, heteroduplex analysis, single-strand conformation polymorphism (SSCP) analysis, and denaturing gradient gel electrophoresis (DGGE), to detect these mutations i...

2004
Güven Uraz Hülya Şimşek

Resistance of Mycobacterium tuberculosis (MTB) to antituberculous drugs has been threatening the public-health grossly. Recently, because of high-level of resistance to rifampicin in MTB, treatment is becoming impossible. In this study, 127 rifampicin resistant and 33 rifampicin susceptible strains were randomly chosen from tuberculosis culture-positive isolates, isolated in the laboratory of t...

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