نتایج جستجو برای: bax/bcl2 gene dosage ratio

تعداد نتایج: 1682967  

Journal: :journal of paramedical sciences 0
mehrdad hashemi department of pharmacology and toxicology, pharmaceutical science branch, islamic azad university, tehran, iran

global cerebral ischemia (gci) and reperfusion induced apoptosis that lead to cell injury and death. the bax and bcl-2 are pro-apoptotic and anti-apoptotic genes, respectively. these genes belong to the b-cell lymphoma-2 (bcl-2) family.in this study; we assessed the effect of pentoxifylline drug on bax/bcl2 gene dosage expression changes following   ischemic reperfusion injury in kidney. in thi...

Journal: :journal of reproduction and infertility 0

background: in recent studies, partial deletions of the azoospermia factor c region (azfc) on the y-chromosome have been detected in males with infertility problems. however, there has been a lot of debate about their significance. in order to study such deletions, a simple but accurate method for their detection was applied in this study. methods: we present data obtained from the multiplex li...

2011
James R. Walters Thomas J. Hardcastle

Dosage compensation--equalizing gene expression levels in response to differences in gene dose or copy number--is classically considered to play a critical role in the evolution of heteromorphic sex chromosomes. As the X and Y diverge through degradation and gene loss on the Y (or the W in female-heterogametic ZW taxa), it is expected that dosage compensation will evolve to correct for sex-spec...

Journal: :BioTechniques 2003
Qiang Liu Xuemin Li Jie Sheng Chen Steve S Sommer

Robust dosage-PCR (RD-PCR) was developed to detect heterozygous large deletions, an important class of mutations missed by conventional PCR strategies. PCR-based methods are available for distinguishing between the dosage of one or two template copies, but general application is limited by the laborious nature of the method and/or the optimization required for each new set of gene exons to be a...

پایان نامه :وزارت علوم، تحقیقات و فناوری - پژوهشگاه ملی مهندسی ژنتیک وزیست فناوری 1389

تالاسمی آلفا شایعترین اختلال ارثی در سنتز هموگلوبین وشایعترین نوع تالاسمی دردنیا می باشد. تفسیر موارد مبتلا به میکروسیتوز ماندگار بدون نشانه های غیر طبیعی دیگر در مشاوره قبل از ازدواج و تشخیص قبل از تولد ایجاد دشواری می نماید. این مطالعه بر روی افراد مشکوک به ناقل جهش در ژن آلفا گلوبین فاقد جهش های شایع آلفا انجام شد. پس از انجام مشاوره ژنتیک، بررسی پرونده بالینی و آزمایشات انجام شده، افراد وا...

Journal: :Clinical Chemistry 1998

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