نتایج جستجو برای: predominant mutations

تعداد نتایج: 215817  

Journal: :Revista de saude publica 2000
A E Guimarães C Gentile C M Lopes A Sant'Anna A M Jovita

OBJECTIVE To assess the mosquito fauna in Serra da Bocaina National Park (PNSB), by collecting information through a general survey, and investigating the population behavior in habitats within the park with different vegetation. METHODS Human bait collections were conducted once a month for both the forest and households, in diurnal and nocturnal periods, three time a day, throughout 24 mont...

1994
Jacques Distler Shamit Kachru Joseph Henry

We use the quantum symmetries present in string compactification on LandauGinzburg orbifolds to prove the existence of a large class of exactly marginal (0,2) deformations of (2,2) superconformal theories. Analogous methods apply to the more general (0,2) models introduced in [1], lending further credence to the fact that the corresponding Landau-Ginzburg models represent bona-fide (0,2) SCFTs....

Journal: :iranian journal of allergy, asthma and immunology 0
sepideh safaei immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran mohammad reza fazlollahi immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran masoud houshmand national institute of genetic engineering biotechnology tehran, iran amir ali hamidieh hematology oncology & stem cell transplantation research center, tehran university of medical sciences, tehran, iran mohammad hassan bemanian department of pediatrics , division of allergy and clinical immunology, shahid sadoghi hospital, shahid sadoghi university of medical sciences, yazd, iran samin alavi department of pediatric hematology-oncology, mofid children's hospital, shahid beheshti university of medical sciences, tehran, iran

wiskott-aldrich syndrome (was) is a life-threatening x-linked recessive immunodeficiency disease described as a clinical triad of thrombocytopenia,  eczema, and recurrent infections, caused by mutations of the was protein (wasp) gene. the milder form of this disease is x-linked thrombocytopenia  (xlt) that  presents only as platelet abnormalities. mutation analysis for 15 boys with wiskott-aldr...

Journal: :مجله علوم اعصاب شفای خاتم 0
leila alizadeh shefa neuroscience research center, khatam alanbia hospital, tehran, iran.

mitochondria are membrane-enclosed organelle found in most eukaryotic cells, which known as power house in cells. this organelle transforms energy into forms that are usable by the cell. the most common psychiatric disorders such as depression and anxiety can be linked to mitochondrial disorders. furthermore, mutations of mitochondrial or nuclear dna (mtdna and ndna, respectively) have been lin...

2017
Mehri Salari Alexander C Lehn Masoud Etemadifar Seyed Amir Hejazi

Chorea-acanthocytosis (ChAc) is an orphan disease, caused by mutations on chromosome 9. Epileptic seizures of mesial temporal origin can be a predominant symptom. We report on a 29-year-old woman with ChAc and bilateral MTS. Previously, few patients with coexisting ChAc and MTS were reported. The underlying pathophysiology is unknown, and further studies are needed.

Journal: :Journal of clinical microbiology 2008
Sun-Hee Cho Hyuk-Joon Kwon Tae-Eun Kim Jae-Hong Kim Han-Sang Yoo Sun-Joong Kim

Fifty-six Newcastle disease virus strains collected from 2000 to 2006 could be grouped into subgenotype VIId. However, they displayed cumulative mutations in and around the linear epitope of hemagglutinin-neuraminidase (residues 345 to 353) with time. The antigenicities of the variants that became predominant in Korea differ from each other and from the wild type.

Journal: :hepatitis monthly 0
rym ayari laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected]; laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected] yousr lakhoua-gorgi laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected] lamjed bouslama borj cedria center for biotechnology, hammam lif, tunisia imen safar laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected] fatma houissa kchouk laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected] houda aouadi laboratory of immunology research center, kidney transplantation and immunopathology (lr03sp01), charles nicolle hospital, university of tunis el manar, tunisia +216-25462623, [email protected]

background in this study, we evaluated the prevalence of the most common mutations occurring in enhancer ii (enhii), basal core promoter (bcp), precore (pc), and core (c) regions of hepatitis b virus (hbv) genome. objectives we also investigated the correlation between hbv variants, their genotypes, and patients’ hbe antigen (hbeag: soluble shape of the capsid antigen) status patients and metho...

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