نتایج جستجو برای: point mutation

تعداد نتایج: 796715  

اکرمی پور, رضا, خالقی, سمیه, علی بخشی, رضا, بیدکی, سید کاظم ,

  Background: Alpha thalassemia is a single gene disorder, inherited in an autosomal recessive manner. The thalassemia occurs mostly in peoples from the Mediterranean to Southeast Asia. The present study was aimed to identify the prevalence of nondeletional Alpha thalassemia mutations in our samples in the Kermanshah province.   Methods : This study included Alpha thalassemia individuals who ha...

Journal: :Physical Chemistry Chemical Physics 2021

Proton transfer along the hydrogen bonds of DNA can lead to creation short-lived, but biologically relevant point mutations that further gene mutation and, potentially, cancer.

Journal: :iranian journal of medical sciences 0
mohammad savari department of medical microbiology, virology & immunology, kerman university of medical sciences, kerman, iran hamid abdollahi department of medical microbiology, virology & immunology, kerman university of medical sciences, kerman, iran mohammad javad zahedi physiology research center and department of gastroentrology, kerman university of medical sciences, kerman, iran sodaif darvish moghadam physiology research center and department of gastroentrology, kerman university of medical sciences, kerman, iran mehdi hayatbakhsh abasi physiology research center and department of gastroentrology, kerman university of medical sciences, kerman, iran

background: clarithromycin resistance in helicbacter pylori has been found to be associated with point mutations in 23s rrna gene leads to reduced affinity of the antibiotic to its ribosomal target or changing the site of methylation. the aim of this study was to determine the most important point mutations in 23s rrna gene in h. pylori that are closely related to clarith-romycin resistance amo...

Journal: :middle east journal of cancer 0
santhi sarojam division of cancer research, regional cancer centre, trivandrum, india sangeetha vijay division of cancer research, regional cancer centre, trivandrum, india sureshkumar raveendran division of cancer research, regional cancer centre, trivandrum, india jayadevan sreedharan gulf medical university, ajman, uae geetha narayanan division of medical oncology, regional cancer centre, trivandrum, india hariharan sreedharan division of cancer research, regional cancer centre, trivandrum, india

background : fms-like tyrosine kinase 3 is a tyrosine kinase receptor that plays an important role in proliferation and differentiation of hematopoietic stem cells. internal tandem duplication and tyrosine kinase domain mutation are the two most common types of fms-like tyrosine kinase 3 mutations frequently reported in acute myeloid leukemia associated with pathogenesis of this disease. the pr...

Journal: :iranian biomedical journal 0
مرجان یغمایی marjan yaghmaie کامران علی مقدم kamran alimoghaddam حسین مزدرانی hossein mozdarani اردشیر قوام زاده ardeshir ghavamzadeh مرجان حاج قاسمی marjan hajhashemi مظفر ازنب mozaffar aznab سید حمداله غفاری

background: the secondary genetic changes other than the promyelocytic leukemia-retinoic acid receptor (pml-rara) fusion gene may contribute to the acute promyelocytic leukemogenesis. chromosomal alterations and mutation of flt3 (fms-like tyrosine kinase 3) tyrosine kinase receptor are the frequent genetic alterations in acute myeloid leukemia. however, the prognostic significance of flt3 mutat...

Journal: :Blood 1992
H Kanno H Fujii A Hirono M Omine S Miwa

We cloned and sequenced the cDNAs for R-type pyruvate kinase (R-PK) from three homozygous PK patients. A point mutation (1151ACG to ATG) identified in the R-PK cDNA of PK Nagasaki was identical with that previously identified in an unrelated family, PK Tokyo. The mutation has also been identified in the PK L gene of a Lebanese family, PK Beirut, by Neubauer et al (Blood 77:1871, 1991). These re...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید