نتایج جستجو برای: tetra arms pcr
تعداد نتایج: 209595 فیلتر نتایج به سال:
A tetra-armed cyclen ( L ) with phenylethynylmethyl groups as side-arms forms ·CH 3 CN inclusion crystals from acetonitrile–organic mixed solvents high selectivity.
Single-nucleotide polymorphism (SNP) genotyping is widely used in genetic association studies to characterize genetic factors underlying inherited traits. Despite many recent advances in high-throughput SNP genotyping, inexpensive and flexible methods with reasonable throughput levels are still needed. Real-time PCR methods for discovering and genotyping SNPs are becoming increasingly important...
خلاصه: سابقه و هدف: عفونتهای پریودنتال همواره جزو شایعترین بیماریهای دهان و دندان است و مهمترین علت از دست رفتن دندانها پس از پوسیدگی محسوب میگردند. هدف از انجام مطالعه حاضر شناسایی و توالییابی باکتریهای ایجادکننده بیماری پریودنتال و ارتباط آن با پلیمورفیسم ژنومی اینترلوکین-6 با روش Tertra-Arms-PCR بود. مواد و روش ها: در این مطالعه مورد-شاهدی، تعداد 100 نمونه پلاک فوق لثهای (50 ...
Human Norovirus is the leading cause of non-bacterial gastroenteritis in children worldwide, and research into it critical for outbreak prevention infection control. The multiplex real time PCR technique was evaluated this study using 100 specimens (stool blood) collected from Al-Muthanna province. RT-Qpcr NVGI NVGII used to test all samples Norovirus. overall incidence rate human 26%, with fir...
jak2 is a tyrosine kinase that plays an important role in the signaling pathways of many hematopoietic growth factor receptors. a single acquired point mutation – v617f – in jak2 occurs in the great majority of patients with polycythemia vera (pv) and approximately half of the patients with idiopathic myelofibrosis (imf) or essential thrombocythemia (et). in contrast, the jak2-v617f mutation is...
schizophrenia is a severe neuropsychiatric disorder with symptoms such as hallucination, delusion and mental disorder. it is a complex disorder, in which genetic components play a crucial role in its pathogenesis. among candidate genes for schizophrenia, neuregulin 1 (nrg1) gene is the most important gene, association of which with the illness has been confirmed in several studies. single nucl...
Background and Aim: Coronary artery disease (CAD) is a multifactorial inherited disorder in which the arteries that blood to the heart muscle become hardened and narrowed. We aimed at investigating the role of rs5186 (A1166C) polymorphism the angiotensin II type 1 receptor (AGTR1) gene as risk factors in some Iranian CAD patients. Materials and Methods: In this case-control study 137 samples...
background and objectives: jak2 is a nonreceptor tyrosine kinase that plays a major role in myeloid disorders. jak2v617f mutation is characterized by a g to t transverse at nucleotide 1849 in exon 12 of the jak2 gene, located on the chromosome 9p, leading to a substitution of valine to phenylalanine at amino acid position 617 in the jak2 protein. in this study we compared two molecular methods ...
Abstract Introduction: Genetic variation of FGFR3 gene is one of the factors affecting the bladder tumor. FGFR3 is a tyrosine kinase receptor, involved in controlling the cellular and angiogenesis cycle. This protein affects a variety of diseases and cancers and cartilage growth abnormalities. Regarding the high activity of fgfr3 mutations in more than 50% of primary tumors of bladder urethral...
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