نتایج جستجو برای: single point mutation

تعداد نتایج: 1576603  

Hamid Najafi Zarini Seyed Kamal Kazemitabar Zahra Ghanei,

The main objective for plant breeding is to increase genetic diversity. Mutation induction is a method to increase genetic diversity associated with selection, recombination, or a combination of these approaches in plant breeding. The present research was aimed to compare efficacy of different doses of Gamma rays (150, 200, 250, 300 and 350 Gy and zero dose control) on the sesame morphological ...

Objective(s): We investigated the contribution of gyrA and parC mutational mechanism in decreased ciprofloxacin susceptibility of Acinetobacter baumannii isolated from burn wound infections. Materials and Methods: Ciprofloxacin susceptibility of 50 A. baumannii isolates was evaluated by disk diffusion and agar dilution methods. PCR and sequencing were performed for detection of mutation in gyr...

Journal: :Scientific Reports 2021

Abstract The interaction between the receptor-binding domain (RBD) of SARS-CoV-2 spike glycoprotein and ACE2 enzyme is believed to be entry point virus into various cells in body, including lungs, heart, liver, kidneys. current focus several therapeutic design efforts explores attempts at affecting binding potential two proteins limit activity disease progression. In this work, we analyze stabi...

Journal: :Gut 1999
I Nishimori M Kamakura K Fujikawa-Adachi M Morita S Onishi K Yokoyama I Makino H Ishida M Yamamoto S Watanabe M Ogawa

BACKGROUND/AIMS Single-point mutations in the cationic trypsinogen gene have been reported in hereditary pancreatitis kindreds in the white population. The aim of the present study was to investigate whether similar gene mutations are present in Japanese hereditary pancreatitis kindreds. METHODS All five exons of the cationic trypsinogen gene were amplified by polymerase chain reaction and se...

Journal: :iranian journal of child neurology 0
mohammad mehdi heidari* 1. department of biology, school of sciences, yazd university, yazd, iran mehri khatami 1. department of biology, school of sciences, yazd university, yazd, iran jafar pourakrami 2. department of biology, faculty of sciences, science and research branch of the islamic azad university, tehran, iran.

how to cite this article: heidari mm , khatami m, pourakrami j. novel point mutations in frataxin gene in iranian patients with friedreich’s ataxia. iran j child neurol. 2014 winter; 8(1):32-36.   objective friedreich’s ataxia is the most common form of hereditary ataxia with autosomal recessive pattern. more than 96% of patients are homozygous for gaa repeat extension on both alleles in the fi...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید