نتایج جستجو برای: gene location

تعداد نتایج: 1340004  

Journal: :acta medica iranica 0
sanambar sadighi department of medical oncology, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. mahsa ghaffari-moghaddam department of medical genetics, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. mojtaba saffari department of medical genetics, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. and departement of medical genetics, school of medicine, tehran university of medical genetics, tehran, iran. mohammad ali mohagheghi department of surgical oncology, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran. reza shirkoohi department of medical genetics, cancer research center, cancer institute of iran, tehran university of medical sciences, tehran, iran

desmoids tumors, characterized by monoclonal proliferation of myofibroblasts, could occur in 5-10% of patients with familial adenomatous polyposis (fap) as an extra-colonic manifestation of the disease. fap can develop when there is a germ-line mutation in the adenomatous polyposis coli gene. although mild or attenuated fap may follow mutations in 5΄ extreme of the gene, it is more likely that ...

Hamid Tebyanian, Hamze farhadian Mehdi Behdani Mohamad Reza Imen Shahidi,

Objective: The Rifampicin resistance and susceptibility of Mycobacterium tuberculosis are caused by mutations in the 81-base pair region of the rpoB gene encoding the b-subunit of RNA polymerase. Methods: Isoniazid resistance of M. tuberculosis is related to mutations in inha , oxyR and ahpC genes which 30 to 90 percent of Isoniazid resistance is occurred in 3015 codons of kat...

Journal: :international journal of advanced biological and biomedical research 2014
hamid tebyanian hamze farhadian mohamad reza imen shahidi mehdi behdani

objective: the rifampicin resistance and susceptibility of mycobacterium tuberculosis are caused by mutations in the 81-base pair region of the rpob gene encoding the b-subunit of rna polymerase. methods: isoniazid resistance of m. tuberculosis is related to mutations in inha , oxyr and ahpc genes which 30 to 90 percent of isoniazid resistance is occurred in 3015 codons of katg gene. the rpob a...

Journal: :the modares journal of electrical engineering 2003
hamidreza noorian kamal mohamedpour

future increase of mobile communication subscribers will require a great capacity expansion of the cellular systems. in order to accommodate the increasing number of subscribers, the cell size will have to be much smaller than current size. therefore, it is predictable that the location updating and paging procedures will produce a major part of signaling traffic in these networks. this pape...

Abolfazl Fateh Ali Karimi Alireza Hadizadeh Tasbiti Farid Abdolrahimi Khaled Seyedi Leonid Petrovich Titov Morteza Ghazanfari Nayereh Ebrahimzadeh Saeed Zaker Bostanabad,

The aim of this study was to investigate the frequency, location and type of rpoB gene mutations in Mycobacterium tuberculosis (MTB) collected from patients in the southern endemic region of Iran. Drug susceptibility testing was determined by using the BACTEC system and the center for diseases control’s (CDC) standard conventional proportional method. In 29 rifampicin-resistant MTB (85%) isolat...

Hamid Tebyanian, Hamze farhadian Mehdi Behdani Mohamad Reza Imen Shahidi,

Objective: The Rifampicin resistance and susceptibility of Mycobacterium tuberculosis are caused by mutations in the 81-base pair region of the rpoB gene encoding the b-subunit of RNA polymerase. Methods: Isoniazid resistance of M. tuberculosis is related to mutations in inha , oxyR and ahpC genes which 30 to 90 percent of Isoniazid resistance is occurred in 3015 codons of kat...

ASGHAR HAGIBEIGI, BEHROOZ BROUMAND, HOSSEIN NAJMABADI, MAHDI M. HAGHIGHI, MINA OHADI, RAMIN RADPOUR,

 ABSTRACT Background: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder with genetic heterogeneity. Up to three loci are involved in this disease, PKDI on chromosome 16p13.3, PKD2 on 4q21, and a third locus of unknown location. Methods: Here we report the first molecular genetic study of ADPKD and the existence oflocus heterogeneity for ADPKD in the Iranian populatio...

Journal: :medical journal of islamic republic of iran 0
ramin radpour department of clinical genetics and infertility, reproductive biomedicine research center of royaninstitute, tehran.iran. mahdi m. haghighi the genetic research center of social welfare and rehabilitation sciences university, tehran mina ohadi the genetic research center of social welfare and rehabilitation sciences university, tehran behrooz broumand rasoul akram hospital, iran university of medical sciences, tehran, iran. hossein najmabadi the genetic research center of social welfare and rehabilitation sciences university, tehran asghar hagibeigi the genetic research center of social welfare and rehabilitation sciences university, tehran

abstract background: autosomal dominant polycystic kidney disease (adpkd) is an inherited disorder with genetic heterogeneity. up to three loci are involved in this disease, pkdi on chromosome 16p13.3, pkd2 on 4q21, and a third locus of unknown location. methods: here we report the first molecular genetic study of adpkd and the existence oflocus heterogeneity for adpkd in the iranian population...

2002
Kentaro Mori Satoshi Fukuchi Ken Nishikawa Katsuhisa Horimoto

1 Japan Registry Service Co., Ltd., 1-2 Kanda-ogawamachi, Chiyoda-ku, Tokyo 1010052, Japan 2 Laboratory for Gene-Product Informatics, The Center for Information Biology and DNA Data Bank of Japan, National Institute of Genetics, Mishima, Shizuoka 4118540, Japan 3 Laboratory of Biostatistics, Human Genome Center, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokane-dai, Minato-ku, ...

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