نتایج جستجو برای: cag a

تعداد نتایج: 13432620  

2013
MD SIDDIQUR RAHMAN YOSHITAKA NAGAI H AKIKO POPIEL MUZAHED UDDIN AHMED

Objective: The study was conducted to find out Spinocerebellar Ataxias (SCA) by genetic analysis from those presenting with parkinsonism in the Neurology department of Mymensingh Medical College. Materials and methods: A sample of about 5ml blood was collected by venipuncture in EDTA tube with informed consent from the patients following institutional ethics committee approval by genetic study ...

2012
S Madjunkova A Eftimov V Georgiev D Petrovski AJ Dimovski D Plaseska-Karanfilska

Prostate cancer (PC) is the second leading cause of cancer deaths in men. The effects of androgens on prostatic tissue are mediated by the androgen receptor (AR) gene. The 5' end of exon 1 of the AR gene includes a polymorphic CAG triplet repeat that numbers between 10 to 36 in the normal population. The length of the CAG repeats is inversely related to the transactivation function of the AR ge...

Journal: :Arquivos de neuro-psiquiatria 2009
Aline Andrade Freund Rosana Hermínia Scola Hélio A G Teive Raquel Cristina Arndt Magda Clara Vieira da Costa-Ribeiro Lupe Furtado Alle Lineu Cesar Werneck

The diagnosis and incidence of spinocerebelar ataxias (SCA) is sometimes difficult to analyze due the overlap of phenotypes subtypes and are disorders of mutations caused by CAG trinucleotide repeat expansion. To investigate the incidence of the SCA in Southern Brazil, we analyzed the trinucleotide repeats (CAG)n at the SCA1, SCA2, SCA3, SCA6 and SCA7 loci to identify allele size ranges and fre...

Journal: : 2021

Compared to transfemoral coronary angiography (CAG), transradial CAG has been associ¬ated with less access site complications, shorter hospitalization, better patient comfort, and early mobilization. However, the use of radial in may also cause entry compli¬cations. Radial pseudoaneurysm after is a rare complication reported than 0.1% procedures. In this report, we present 78-year-old who was d...

Journal: :Journal of clinical pathology 2001
T M Peters R J Owen E Slater R Varea E L Teare S Saverymuttu

AIMS To investigate variation within the cag pathogenicity island (PAI) of Helicobacter pylori isolated from patients with dyspepsia in mid-Essex, and to evaluate the effect on expression of anti-CagA antibody. METHODS Sixty two isolates of H pylori cultured from gastric biopsies were screened by specific PCR assays for the presence of cagA and other gene markers (cagD and cagE, and virD4) in...

2006
Ryan A. Irvine Mimi C. Yu Ronald K. Ross Gerhard A. Coetzee

The androgen receptor genotype was determined in the white blood cell DNA of 45 African-American, 39 non-Hispanic white, and 39 Asian (Chinese, Japanese) normal subjects and 68 patients with prostate cancer (57 whites), all of whom were residents of Los Angeles County. For each subject, we measured the number of repeats in the polymorphic CAG and GGC microsatellites of exon 1 of the androgen re...

Journal: :genetics in the 3rd millennium 0
امید آریانی omid aryani special medical center, tehran, iran سپیده دادگر sepideh dadgar special medical center, tehran, iran مسعود هوشمند massoud houshmand special medical center, tehran, iran فرهاد عصارزادگان farhad assarzadegan neurology department, imam hossein hospital, shahid beheshti university of medical sciences, tehran, iran

huntingtons disease is caused by a dominantly transmitted cag repeat expansion mutation that is believed to confer a toxic gain of function on the mutant protein. huntingtons disease patients with two mutant alleles are very rare. in other poly (cag) diseases such as the dominant ataxias, inheritance of two mutant alleles causes a phenotype more severe than in heterozygotes. in our evaluation, ...

Journal: :Oncology reports 2010
Xiao-Ying Teng Gui-Qiu Liu Xiao-Li Diao Zong-Yong Wu Lan Li Wei Zhang Xun Zhang Qin Su

Preferential occurrence of pulmonary, esophageal and bladder carcinomas in males indicate a possible involvement of androgen receptor (AR)-mediated functions. We evaluated the roles of the CAG repeat polymorphism in AR exon 1 in development of these lesions. The exon 1 of AR gene was amplified in samples from 198 male patients with lung carcinoma, 183 with esophageal carcinoma, 95 with bladder ...

Journal: :Human molecular genetics 1997
J E Nielsen P Koefoed K Abell L Hasholt H Eiberg K Fenger E Niebuhr S A Sørensen

CAG repeat expansions have been identified as the disease-causing dynamic mutations in the coding regions of genes in several dominantly inherited neurodegenerative disorders, including spinobulbar muscular atrophy, Huntington's disease, dentatorubral-pallidoluysian atrophy, spinocerebellar ataxia type 1, 2 and 6 and Machado-Joseph disease. The CAG repeat expansions are translated to elongated ...

Journal: :iranian journal of public health 0
m douraghi dept. of pathobiology, school of public health, tehran university of medical sciences, iran m mohammadi helicobacter pylori research group, biotechnology research center, pasteur institute of iran, tehran mh shirazi dept. of pathobiology, school of public health, tehran university of medical sciences, iran a oghalaie helicobacter pylori research group, biotechnology research center, pasteur institute of iran, tehran s saberi kashani helicobacter pylori research group, biotechnology research center, pasteur institute of iran, tehran ma mohagheghi cancer research center, tehran university of medical sciences, iran

background: to asses the status of two representative genes of cag pai i.e caga and cage of helicobacter pylori strains infecting iranian patients suffered from various clinical outcomes using one-step pcr. methods: a total of 120 h. pylori infected patients including non-ulcer dyspepsia, nud (n=81), peptic ulcer disease, pud (n=17), and gastric carcinoma, gc (n= 22) referred for endoscopy or g...

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