نتایج جستجو برای: single point mutation

تعداد نتایج: 1576603  

ذاکر کیش, مهرنوش, سمرباف زاده, علیرضا, مروج آل‌علی, ارمغان, مولا, کریم,

Background: Behcet’s disease (BD) is a multisystemic inflammatory disease with unknown origin characterized by recurrent oral aphtous ulcers, genital, ocular and skin lesions. A single point mutation 1691G to A in the factor V gene increases the risk of venous thrombosis. This study designed to determine factor V Leiden mutation in Behcet’s disease, and to find out it's relationship with the cl...

A Ghavamzadeh, A Zaghal, B Bahar, B Chahardouli, H Dargahi, K Alimoghaddam, N Einollahi, P Karimzadeh, SA Mousavi, SH Ghaffari,

Abstract Objective JAK2 is a non-receptor 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. Methods In this study we evaluated RNA from 89 pati...

Journal: :iranian journal of basic medical sciences 0
azadeh lohrasbi nejad department of biotechnology, research institute for environmental sciences, international centre for science, high technology and environmental sciences, kerman, iran mohammad mehdi yaghoobi department of biotechnology, research institute for environmental sciences, international centre for science, high technology and environmental sciences, kerman, iran

objective(s) p53 is an important tumor suppressor, which is mutated in later stages of many cancers and leads to resistance to chemotherapy. the aim of this study was to reveal mutations of tp53 in colorectal cancer in kerman province. materials and methods a total of forty-three colon cancer specimens as paraffin block or fresh tissues, which passed stage iiia, were selected. three exons 5, 7 ...

Journal: :iranian journal of neurology 0
mohammad mehdi heidari department of biology, school of science, yazd university, yazd, iran mehri khatami department of biology, school of science, yazd university, yazd, iran shahriar nafissi department of neurology, school of medicine, tehran university of medical sciences, tehran, iran faezeh hesami-zokai department of biology, school of science, yazd university, yazd, iran afshin khorrami department of biology, school of science, yazd university, yazd, iran

background: non-dystrophic myotonias are a heterogeneous set of skeletal, muscular channelopathies, which have been associated with point mutations within sodium channel α-subunit (scn4a) gene. because exons 22 and 24 of scn4a gene are recognized as hot spots for this disease, the purpose of the study is to identify mutation in exons 22 and 24 of scn4a gene in iranian non-dystrophic myotonias p...

Voet Th

The nature and pace of genome mutation is largely unknown. Standard methods to investigate DNA-mutation rely on arraying or sequencing DNA from a population of cells, hence the genetic composition of individual cells is lost and de novo mutation in cell(s) is concealed within the bulk signal. We developed methods based on (SNP-) arraying and next-generation sequencing of single-cell whole-genom...

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