نتایج جستجو برای: tetra arms

تعداد نتایج: 35748  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه فردوسی مشهد 1388

جستجوی ژنولوژیکی، فرایند پیچیده ای می باشد که با استفاده از سوابق تاریخی و گهگاه آنالیز ژنتیکی، به اثبات خویشاوندی افراد می پردازد. از آنجا که ژنوم انسان، دارای بخشی از اطلاعات است که تقریبا بدون تغییر از نیاکان اولیه، نسل به نسل منتقل می شوند، از آنالیز همین بخش از dna به منظور جستجوهای ژنولوژیکی استفاده می شود. single nucleotide polymorphism یا snp ها، فراوانترین شکل از پلی مورفیسم های dna ا...

ژورنال: مجله دندانپزشکی 2020

Background and Aims: Periodontitis is one of the most common causes of damage to the gums and retaining structures of the teeth. Matrix protein, a metalloproteinase, is known as intermediate collagenase and the enzyme collagenase fibroblast, which is encoded in humans by the MMP-1 gene. The aim of this study was to investigate 1G/2G polymorphism in the MMP-1 gene and its association with the pe...

Journal: :Journal of Investigative Dermatology 2023

Oxidative stress has been recognized to be associated with melanoma. We have previously shown that ankyrin repeat-rich membrane spanning (ARMS), a tetra-spanning transmembrane protein, was overexpressed in melanoma cells and conferred resistance hydrogen peroxide (H2O2)-induced cell death. To explore the molecular mechanism of ARMS under oxidative stress, we established ARMS-knockdown (siARMS) ...

Journal: :basic and clinical cancer research 0
samaneh hajihoseiny majid motovali-bashi mahnaz roaei

abstract

2008
Shu-Xian Li Lin Zhu Hoong-Kun Fun Suchada Chantrapromma

In the title mol-ecule (systematic name: methane-tetra-yltetra-methyl-ene tetra-p-toluene-sulfonate), C(33)H(36)O(12)S(4), the central C atom and the S atoms exhibit distorted tetra-hedral configurations. The aromatic rings in opposite arms are nearly parallel to each other, with a dihedral angle of 10.26 (8) or 3.45 (9)°. The mol-ecules are linked into a two-dimensional network parallel to the...

Background: The transversion of G to T (G894T) in human endothelial nitric oxide synthase (eNOS) gene has profound effects such as male infertility, recurrent miscarriage, multiple sclerosis and cardiovascular diseases.Objectives: Development of a new Multiplex Tetra-Primer Amplifi cation Refractory Mutation System - Polymerase Chain Reaction (T-ARMS-PCR) for detection of...

Journal: :Turkish Journal of Agricultural and Natural Science 2022

Potato virus Y biberde enfeksiyon oluşturan en yaygın virüslerden bir tanesidir. Bu çalışmada, 23 biber çeşidi ve 30 ıslah hattının PVY-0 PVY-1 patotiplerine karşı reaksiyonları belirlenmiş pvr2 lokusundaki allel genleri mekanik inokulasyon moleküler yöntemler ile belirlenmeye çalışılmıştır. Her çeşit hatta ait dörder bitki, patotipleri ayrı inokule edilmiştir. İnokule edilen bitkiler, virüs si...

Journal: :Heliyon 2023

Due to the genetic mutation (fa) in gene encoding for leptin receptor, homozygous Zucker rats (fa−/−) develop excessive adiposity and become an experimental animal model obesity metabolic-related diseases research. Based on tetra-primer amplification refractory system-polymerase chain reaction (ARMS-PCR), we developed a method quickly genotype with mutated fa allele from their wildtype litterma...

Journal: :gene, cell and tissue 0
ebrahim miri-moghaddam genetics of non-communicable disease research center, zahedan university of medical sciences, zahedan, ir iran; department of genetics, zahedan university of medical sciences, zahedan, ir iran yasaman garmie department of biology, faculty of science, sistan and balouchestan university, zahedan, ir iran majid naderi genetics of non-communicable disease research center, zahedan university of medical sciences, zahedan, ir iran; genetics of non-communicable disease research center, ali-asghar hospital, azadi ave., zahedan, ir iran. tel: +98-5413414567, fax: +98-5413218998

background congenital factor xiii (fxiii) deficiency is a rare severs autosomal recessive bleeding disorder. objectives the aim of the study was to determine the c559t > c fxiiia genotype frequency in patients with fxiii hemophilia who lived in sistan and balouchestan province in southeast of iran. patients and methods we determined the genotype of 180 patients with factor xiii hemophilia by te...

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