نتایج جستجو برای: mutation detection

تعداد نتایج: 844642  

Journal: :Technical Tips Online 1998

Journal: :iranian journal of allergy, asthma and immunology 0
sepideh safaei immunology, asthma & allergy research institute , children’s medical center, tehran university of medical sciences, tehran, iran zahra pourpak immunology, asthma & allergy research institute , children’s medical center, tehran university of medical sciences, tehran, iran mostafa moin immunology, asthma & allergy research institute , children’s medical center, tehran university of medical sciences, tehran, iran massoud houshmand national institute for genetic engineering and biotechnology, tehran, iran

scid disorder is major failure of the immune system, usually genetic. the aim of this study was on mutations detection of rag1, rag2, and il7rg genes in scid cases. mutation detection was performed by pcr sequencing. our results  indicated  that 13  mutations  were found  through  cases which  include 4 mutations in il7r gene (t661i, i138v, t56a, c57w), 7 mutations in rag1 (w896x, w204r, m324v,...

Journal: :The American Journal of Human Genetics 2005

Journal: :international journal of hematology-oncology and stem cell research 0
mehrdad payandeh medical biology research center, kermanshah university of medical sciences, kermanshah, iran. farhad shaveisi zadeh department of medical genetics, faculty of medicine, shahid beheshti university of medical sciences and health services, tehran mohammad erfan zare medical biology research center, kermanshah university of medical sciences, kermanshah, iran; studen kamran mansouri medical biology research center, kermanshah university of medical sciences, kermanshah, iran; depart reza khodarahmi medical biology research center, kermanshah university of medical sciences, kermanshah, iran; depart saeed alimoradi paramedical faculty, kermanshah university of medical sciences, kermanshah, iran

introduction: the myeloproliferative neoplasms (mpns) are a heterogeneous group of diseases characterized by excessive production of blood cells by  hematopoietic precursors. typically, they include polycythemia vera (pv), essential thrombocythemia (et), idiopathic myelofibrosis(imf), and chronic myeloid leukemia (cml). philadelphia chromosome is the final diagnostic test for cml. recently, jak...

Journal: :The Ulster Medical Journal 1997
Patrick J Morrison

Since the original description of Helicobacter plvori by Warren and Marshall in 1983 there has been a virtual explosion in interest in this organism. It is now causally linked to chronic gastritis, peptic ulcer disease, gastric mucosa-associated lymphoid tissue lymphoma and possibly gastric cancer. It has proved to be the single most important advance in modern gastroenterology. This book is a ...

Journal: :middle east journal of cancer 0
hind dehbi genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco yaya kassogue genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco sanaa nasserddine genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco asma quessar department of onco-hematology, ibn rochd university hospital, casablanca, morocco sellama nadifi genetics and molecular pathology laboratory, medical school of casablanca, hassan ii university, casablanca, morocco

background :according to numerous studies, fms-like tyrosine kinase 3, internal tandem duplication, and the d835 mutation are associated with a poor prognostic clinical outcome in acute myeloid leukemia patients. detection of the fms-like tyrosine kinase 3 mutation in patients who present with normal karyotype acute myeloid leukemia helps in both the understanding of the disease and the treatme...

2011

addressed the feasibility of obtaining sensitive, accurate, and reproducible mutation detection results in synthetic templates, cell lines, and FFPE tissue samples using TaqMan Mutation Detection Assays. Analytical performance assessed with synthetic templates and genomic DNA (gDNA) extracted from cell lines or model FFPE cell lines indicates that TaqMan Mutation Detection Assays have a minimum...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه اصفهان - دانشکده علوم 1387

چکیده ندارد.

Journal: :Theoretical Computer Science 2023

Two mechanisms have recently been proposed that can significantly speed up finding distant improving solutions via mutation, namely using a random mutation rate drawn from heavy-tailed distribution (“fast mutation”, Doerr et al. (2017) [2]) and increasing the strength based on stagnation detection mechanism (Rajabi Witt (2020) [3]). Whereas latter obtain asymptotically best probability of singl...

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