نتایج جستجو برای: mutations

تعداد نتایج: 172787  

Journal: :hepatitis monthly 0
masood ziaee hepatitis research center, birjand university of medical sciences, birjand, ir iran davod javanmard hepatitis research center, birjand university of medical sciences, birjand, ir iran; hepatitis research center, birjand university of medical sciences, ghafari ave., birjand, ir iran. tel/fax: +98-5632433004 gholamreza sharifzadeh hepatitis research center, birjand university of medical sciences, birjand, ir iran mohammad hasan namaei hepatitis research center, birjand university of medical sciences, birjand, ir iran ghodsiyeh azarkar hepatitis research center, birjand university of medical sciences, birjand, ir iran

objectives the present study aimed to evaluate the genotypes and prevalence of mutations in a segment of s and rt gene in hbv isolates in southern khorasan, iran. methods this was a population-based study comprising 5,235 randomized samples for hbv screening. a nested-polymerase chain reaction (pcr) test was followed by direct sequencing, and the sequences blast with present sequences of ncbi d...

1997
Shamit Kachru

We find M-theory (Type IIA) duals for compactifications of the 9d CHL string to 5d (4d) on K3 (K3 × S 1). The IIA duals are Calabi-Yau orbifolds with nontrivial RR U (1) In ten dimensions, the consistent critical string theories with (at least) sixteen super-charges have been known since the 1980s. There are (after accounting for the S-duality of the two SO(32) theories) four. In D = 9, in addi...

2001
M. Koniorczyk V. Bužek J. Janszky

We present a unified approach to quantum teleportation in arbitrary dimensions based on the Wigner-function formalism. This approach provides us with a clear picture of all manipulations performed in the telepor-tation protocol. In addition within the framework of the Wigner-function formalism all the imperfections of the manipulations can be easily taken into account. All quantum mechanical ph...

Acharya N Prasad, Prasad P, Sharma Sharma N SharmaU Singh M Singh SK

Background: Mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene can cause congenital bilateral absence of vas deferens. Yet, the spectrum and frequency of CFTR mutations in Indian males with congenital absence of vas deferens (CAVD) is unknown. Materials and Methods: We investigated 50 Indian males, diagnosed with unilateral or bilateral absence of vas deferens at t...

1997
WRAY R. JOHNSON

I N 1994 AIR FORCE Special Opera tions Com mand stood up the 6th Special Op­ era tions Squadron (6 SOS), the first-­ ever USAF squadron dedicated to the for eign inter nal defense (FID) mission area. With roots in special air warfare dating back to the Vietnam War and even as far back as the Second World War, the 6 SOS was created to advise, train, and assist for­ eign aviation forces in the ap...

احمدی, محمدحسین, امیری‌‌زاده, ناصر, ساروخانی, محمدرضا,

   Background and Aim: About 13 beta-globin mutations encompass 70-90% of the mutation spectrum in Iran. These mutations are called common beta-globin mutations. The rest are rare or unknown mutations. The objective of this study was to identify the rare or unknown beta-globin mutations in Qazvin province.   Materials and Methods: In this descriptive-analytic study, EDTA-containing venous blood...

آقائی پور, مهناز , دکتر قاسم رستگار لاری, قاسم, ذاکر, فرهاد , محمدزاده, محمد ,

   Background & Aim: Mutations in c-kit gene cause autonomously proliferation of leukemic cells with an unfavorable prognosis.These mutations including exon 8 deletion and insertion in the fifth extracellular Ig-like domain and exon 17 point mutation in tyrosine kinase domain of c-kit receptors are important in acute myeloid leukemia. The aim of this study was to set up molecular diagnosis and ...

Journal: :hepatitis monthly 0
soad ghabeshi blood transfusion research center, high institute for research and education in transfusion medicine, ir iran +98-2188601501-30, [email protected]; department of microbiology, faculty of biological sciences, shahid beheshti university, ir iran zohreh sharifi blood transfusion research center, high institute for research and education in transfusion medicine, ir iran +98-2188601501-30, [email protected]; blood transfusion research center, high institute for research and education in transfusion medicine, ir iran +98-2188601501-30, [email protected] seyed masoud hosseini department of microbiology, faculty of biological sciences, shahid beheshti university, ir iran mahmood mahmoodian shooshtari blood transfusion research center, high institute for research and education in transfusion medicine, ir iran +98-2188601501-30, [email protected]

background more than two billion people have been exposed to hepatitis b virus (hbv) worldwide. furthermore, four hundred million of them are infected with chronic hbv infection. the predominant mutation of the precore region involves a g to a change at nucleotide1896, which creates a premature stop codon at codon 28. two mutations of a1762t and g1764a are reported as the most prevalent mutatio...

Journal: :international journal of pediatrics 0
rahime renda antalya research and education hospital, pediatric nephrology department, antalya, turkey. özlem aydoğ ankara dr.sami ulus research and education hospital, pediatric nephrology department, ankara, turkey. mehmet bülbül ankara dr.sami ulus research and education hospital, pediatric nephrology department, ankara, turkey. evrim kargın çakıcı ankara dr.sami ulus research and education hospital, pediatric nephrology department, ankara, turkey.

background and aim: steroid-resistant nephrotic syndrome (srns) accounts for 10%-20% of all cases of idiopathic nephrotic syndrome. these patients are at risk of developing end-stage renal disease. the aim of this study was to determine the demographic characteristics, renal biopsy findings, response to immunosuppressive treatment, and prognosis in pediatric patients with srns.materials and met...

Journal: :iranian journal of allergy, asthma and immunology 0
fatemeh ramezani hepatitis b molecular laboratory, department of virology, school of public health, tehran university of medical sciences, tehran, iran mehdi norouzi hepatitis b molecular laboratory, department of virology, school of public health, tehran university of medical sciences, tehran, iran gholam reza sarizade khoozestan province blood trasfusion, ahvaz, iran vahdat poortahmasebi hepatitis b molecular laboratory, department of virology, school of public health, tehran university of medical sciences, tehran, iran ebrahim kalantar gholhak medical laboratory, tehran, iran lars magnius virological department, swedish institute for infectious disease control, solna, sweden

mutations in the human hepatitis b virus (hbv) genome contribute to its escape from host immune surveillance and result in persistent infections. the aim of this study was to characterize the molecular variations of the surface gene and protein in chronically-infected patients from the southern part of iran. the  surface  genes  from  12  hbv  chronic  carriers  were  amplified, sequenced  and ...

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