نتایج جستجو برای: cag repeats length

تعداد نتایج: 331727  

2014
Daniel J Mettman Merlin G Butler Albert B Poje Elizabeth C Penick Ann M Manzardo

OBJECTIVE The androgen receptor (AR) gene, located on the X chromosome, contains a common polymorphism involving cytosine-adenine-guanine (CAG) repeats, which impacts disease and could contribute to the unequal sex ratio in alcoholism. CAG repeats in the AR gene are known to correlate with impulsivity in males. We report the first preliminary study examining the association between the number o...

Objective(s) Varicocele is associated with impaired testicular function and male infertility, but the molecular mechanisms by which fertility is affected have not been satisfactorily explained. The aim of our study was to investigate whether or not the polymerase gamma (POLG) polymorphism is associated with Iranian varicocele patients.    Materials and Methods We determined the POLG CAG repe...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2002
Chu Chen Najib Lamharzi Noel S Weiss Ruth Etzioni Douglas A Dightman Matt Barnett Dante DiTommaso Gary Goodman

The human androgen receptor gene contains polymorphic CAG and GGC repeats in exon 1. We investigated whether the number of CAG and/or GGC repeats is related to prostate cancer risk in a case-control study nested within the beta Carotene and Retinol Efficacy Trial. Among 300 cases and 300 controls, we did not observe any increase in risk associated with fewer CAG or GGC repeats. We observed a no...

Journal: :Archives of neurology 2011
Hussein Daoud Véronique Belzil Sandra Martins Mike Sabbagh Pierre Provencher Lucette Lacomblez Vincent Meininger William Camu Nicolas Dupré Patrick A Dion Guy A Rouleau

OBJECTIVE To analyze the ataxin 2 (ATXN2) CAG repeat size in a cohort of patients with amyotrophic lateral sclerosis (ALS) and healthy controls. Large (CAG)(n) alleles of the ATXN2 gene (27-33 repeats) were recently reported to be associated with an increased risk of ALS. DESIGN Case-control study. SETTING France and Quebec, Canada. PARTICIPANTS A total of 556 case patients with ALS and 4...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2010
Justus L Groen Rob M A de Bie Elisabeth M J Foncke Raymund A C Roos Klaus L Leenders Marina A J Tijssen

Huntington disease (HD) is a neurodegenerative disorder associated with an expanded CAG trinucleotide repeat length in the huntingtin gene. 'Intermediate alleles' with 27 to 35 CAG repeats generally do not cause HD but are unstable upon germ-line transmission. Insights in CAG repeat mosaicism and enhanced trinucleotide expansion in postmitotic neurons indicate that in the intermediate range, ot...

Journal: :international journal of reproductive biomedicine 0
mohamad moghadam saied reza khatami hamid galehdari

background: androgens play critical role in secondary sexual and male gonads differentiations such as spermatogenesis, via androgen receptor. the human androgen receptor (ar) encoding gene contains two regions with three nucleotide polymorphic repeats (cag and ggn) in the first exon. unlike the cag repeats, the ggn has been less studied because of technical difficulties, so the functional role ...

Journal: :Turkish journal of medical sciences 2017
Mahmoud Shekari Khaniani Parisa Aob Mohammadreza Ranjouri Sima Mansoori Derakhsan

Background/aim: Huntington disease (HD) is a progressive adult-onset neurodegenerative disorder presenting an autosomal dominant inheritance. Since there is no information on the prevalence of HD in northwestern Iran, the aim of the present study was to determine the prevalence of HD and the number of CAG trinucleotide repeats in the population of northwestern Iran.Materials and methods: Genomi...

Journal: :American journal of human genetics 1999
T R Rebbeck P W Kantoff K Krithivas S Neuhausen M A Blackwood A K Godwin M B Daly S A Narod J E Garber H T Lynch B L Weber M Brown

Compared with the general population, women who have inherited a germline mutation in the BRCA1 gene have a greatly increased risk of developing breast cancer. However, there is also substantial interindividual variability in the occurrence of breast cancer among BRCA1 mutation carriers. We hypothesize that other genes, particularly those involved in endocrine signaling, may modify the BRCA1-as...

Journal: :Clinical biochemistry 1999
B S Bharaj E J Vassilikos E P Diamandis

OBJECTIVES To develop and evaluate a new method for determination of the CAG repeat length in Exon 1 of the androgen receptor gene. DESIGN AND METHODS The method is based on PCR amplification of a DNA region encompassing the repeats and analysis of the length of the PCR product on a sequencing gel. One of the PCR primers was labeled with Cy5.5 fluorescent dye to facilitate detection after las...

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