ارتباط تنوع ژن shank3 و بیماری اوتیسم

بررسی ارتباط پلی‌مرفیسم‌های ژن TNF-α و بیماری سل ریوی

Background and Objective: Tuberculosis (TB) caused by Mycobacterium tuberculosis, is an infectious disease in human which kills nearly three millions of people annually. Approximately, one - third of the world populations are infected with this bacteria and 5 - 10 % of them develop the active form of the disease. Individuals are different in susceptibility to TB infection. These differences mig...

شناسایی تنوع ژنتیکی در دو ژن کاندیدا TLR2، TNFα و ارتباط آن با بیماری ورم پستان در گاو هلشتاین

Mastitis is one of the most common diseases in dairy cattle, which has imposed therapy heavy costs to farmers through significant reduction in total milk production. Identification of nucleotide polymorphism of two candidate immunity response genes and its effects on SCS as a mastitis incidence indicator was carried out in this research. The genes were exons 1 and 2 of TLR2 and 3 and 4 of TNFα....

بررسی ارتباط ژن RANTES با بیماری عروق کرونری قلب

ارتباط پلی مورفیسم (C677T ) ژن MTHFR با بیماری عروق کرونری

Background and purpose: Coronary artery disease (CAD) is a complex disease that is caused by both environmental and genetic factors. Methylenetetrahydrofolate (MTHFR) enzyme is associated with metabolism of homocysteine and its impaired function is considered as a risk factor for developing CAD. Some variants are involved in decreased activity of MTHFR and its deficiency. The polymorphism of C6...

SHANK3, the synapse, and autism.

Autism spectrum disorders present a paradox of great heterogeneity and great specificity. Well over 100 genetic disorders yield an autism phenotype,1 most through specific but distinct mechanisms, and many of which affect the synapse. SHANK3 (SH3 and multiple ankyrin repeat domains 3) is known to be disrupted in the 22q13 deletion syndrome (Phelan–McDermid syndrome), and variants of SHANK3 have...

بررسی تنوع ژنتیکی ژن هایhsp70 و enos در بیماری گلوکوم

گلوکوم یکی از علل نابینایی غیرقابل برگشت در سراسر جهان است. پروسه بیماری با تحلیل سلول های آپاپتوتیگ شبکیه و آسیب عصب بینایی مشخص می شود. گلوکوم یک بیماری چند عاملی است و هر دو عامل محیطی و ژنتیکی در پیشرفت بیماری قابل توجه اند. نیتریک اکسید (no) مولکول بیولوژیک فعالی است که در فرآیند های فیزولوژیکی مختلفی از جمله انتقال عصبی، تنظیم حجم عروق و آپاپتوزیس دخیل می باشد. no گردشی در شبکیه توسط آنزی...