نتایج جستجو برای: induced mutation

تعداد نتایج: 1234912  

Microtubule Affinity-Regulating Kinase 2 (MARK2) protein has a substantial role in regulation of vital cellular processes like induction of polarity, regulation of cell junctions, cytoskeleton structure and cell differentiation. The abnormal function of this protein has been associated with a number of pathological conditions like Alzheimer disease, autism, several carcinomas and development of...

Journal: :iranian journal of public health 0
yu-feng wen school of public health, wan nan medical college, wuhu, china. chao jiang school of public health, wan nan medical college, wuhu, china. xian-feng cheng school of public health, wan nan medical college, wuhu, china. zhi-ping zhang centre for disease prevention and control of anqing city, anqing, china. bai-feng chen school of public health, wan nan medical college, wuhu, china. yu zhu school of public health, wan nan medical college, wuhu, china.

the miru-vntr polymorphism and katg463 mutation are used to genotype the mycobacterium tuberculosis, but the correlation between them and inh-resistance were unknown. this study was aimed to explore whether etre polymorphism and katg463 mutation could predict the inh-resistance, and the relationship between etre polymorphism and katg463 mutation.the etre, katg463 mutation and drug resistance in...

Journal: :international journal of reproductive biomedicine 0
zohreh hojati somaye heidari majid motovali-bashi

background: about 10% of infertilities with obstructive azoospermia are congenital and caused by cf gene mutations. m469i mutation was observed for the first time in taiwanese patients. this mutation not only causes cf, but also may be the origin of infertility too. objective: in this study, we aimed in designing a rapid, reliable rflp-pcr procedure for detection of m469i mutation. the correlat...

Journal: :OBM genetics 2023

Lung cancer is a leading cause of death among all the worldwide and it has highest occurrence mortality rates. <em>Mycobacterium</em> <em>tuberculosis</em> (MTB) induced tuberculosis been known as one risk factors for lung carcinogenesis. The exact mechanism MTB understood to date. Several research epidemiological studies about link between exist. It proposed that causes...

Journal: :Biodiversitas 2023

Abstract. Ishak I. 2023. Genetic variability of mutant rice (Oryza sativa) genotype induced by gamma rays. Biodiversitas 24: 3300-3306. Rice seeds Sidenuk cultivars were irradiated rays creating a broad spectrum genetic among individual plants at M3 generation progeny. Gamma Irradiated created Mutation the somatic cells population in mature embryos M1 generations. Somatic cell mutation influenc...

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2006
Marcus A Jackson Isabel Lea Asif Rashid Shyamal D Peddada June K Dunnick

Mutational incidence and spectra for genes examined in both human and mouse lung and liver tumors were analyzed using the National Institute of Environmental Health Sciences (NIEHS) Genetic Alterations in Cancer (GAC) knowledge system. GAC is a publicly available, web-based system for evaluating data obtained from peer-reviewed studies of genetic changes in tumors associated with exposure to ch...

آبسواران, ابوالفضل, اسماعیلی, محسن, جبارپور بنیادی, مرتضی, لطفلیزاده, نادر, یونس پور, رضا,

Background and Objective: Profound hearing loss is one of the most prevalent congenital disorders affecting about 1 in 1000 newborns. Autosomal recessive non-syndromic hearing loss (ARNSHL) is the predominant form of the severe inherited childhood deafness. This type of hearing loss in one-half of the cases is caused by mutations in GJB2 (connexin 26) and GJB6 (connexin 30) genes located at DFN...

Journal: :iranian journal of public health 0
samaneh hajihoseini genetics division, dept. of biology, faculty of sciences, university of isfahan, isfahan, iran. majid motovali-bashi genetics division, dept. of biology, faculty of sciences, university of isfahan, isfahan, iran. mohammad amin honardoost molecular and cellular division, dept. of biology, faculty of sciences, university of isfahan, isfahan, iran. nader alerasool genetics division, dept. of biology, faculty of sciences, university of isfahan, isfahan, iran.

β-thalassemia, a monogenic autosomal recessive disorder, is prevalent in middle east, particularly in iran. in iran, near to 20 mutations in the β-globin gene are introduced as common mutations with varying incidence frequencies in each city. therefore, detection and screening for couples at high risk can help to solve the problems of this disease. in this study, optimized genotyping of two com...

ژورنال: پیاورد سلامت 2008
توگه, غلام رضا, علی مقدم, کامران, عین اللهی, ناهید, غفاری, سید حمیداله, فردوسی, شیرین, قوام زاده, اردشیر, موسوی, سید اسد اله, نادعلی, فاطمه, چاردولی, بهرام,

Background and Aim : Myeloproliferative neoplasms are clonal and heterogeneous disorders of hematopoietic stem cells lead to increase of one or more cell lines in the blood. Recently, the acquired mutation JAK2 V617F has been described in the majority of patients with myeloproliferative neoplasms (MPNs).This mutation is characterized by a G to T transverse at nucleotide 1849 in exon 12 of the J...

LEILI YAZDCHI -MARANDI, PHILIPPE POUSSIER, SHEELA RAMANATHAN,

The BioBreeding- Diabetes Prone (BB-DP) rat spontaneously develops an autoimmune diabetic syndrome that is dependent on the RT1 u Major Histocompatibility Complex (MHC) haplotype and homozygosity for an allele at the Lymphopenia (Lyp) locus. Lyp mutation is responsible for a peripheral T -lymphopenia. There are other genetic loci contributing to diabetes susceptibility in this strain. BB ra...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید