نتایج جستجو برای: cag repeats

تعداد نتایج: 27776  

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: :Journal of the National Cancer Institute 2000
M W Yu S W Cheng M W Lin S Y Yang Y F Liaw H C Chang T J Hsiao S M Lin S D Lee P J Chen C J Liu C J Chen

BACKGROUND Worldwide, hepatocellular carcinoma (HCC) is more prevalent in men than in women, suggesting that sex hormones and/or X-chromosome-linked genes may be involved in hepatocarcinogenesis. We investigated the association of a trinucleotide (CAG) repeat in the androgen receptor (AR) gene (located on the X chromosome) termed "AR-CAG repeats," levels of plasma testosterone, and the risk of ...

2011
Daniel Duzdevich Jinliang Li Jhoon Whang Hirohide Takahashi Kunio Takeyasu David T. F. Dryden A. Jennifer Morton J. Michael Edwardson

BACKGROUND In the R6/2 mouse model of Huntington's disease (HD), expansion of the CAG trinucleotide repeat length beyond about 300 repeats induces a novel phenotype associated with a reduction in transcription of the transgene. METHODOLOGY/PRINCIPAL FINDINGS We analysed the structure of polymerase chain reaction (PCR)-generated DNA containing up to 585 CAG repeats using atomic force microscop...

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 ...

Journal: :Human molecular genetics 1999
T Sato M Oyake K Nakamura K Nakao Y Fukusima O Onodera S Igarashi H Takano K Kikugawa Y Ishida T Shimohata R Koide T Ikeuchi H Tanaka N Futamura R Matsumura T Takayanagi F Tanaka G Sobue O Komure M Takahashi A Sano Y Ichikawa J Goto I Kanazawa

Dentatorubral-pallidoluysian atrophy (DRPLA) is one among an increasing number of hereditary neurodegenerative diseases determined as being caused by unstable expansion of CAG repeats coding for polyglutamine stretches. To investigate the molecular mechanisms underlying CAG repeat instability, we established three transgenic lines each harboring a single copy of a full-length human mutant DRPLA...

Journal: :Molecular human reproduction 2004
A Ferlin L Bartoloni G Rizzo A Roverato A Garolla C Foresta

The androgen receptor (AR) has two polymorphic sites in exon 1, characterized by different numbers of CAG and GGC repeats resulting in variable lengths of polyglutamine and polyglycine stretches. Longer CAG repeats result in a reduced AR transcriptional activity, whereas the role of the GGC triplets is less clear. A relationship between decreased spermatogenesis and moderate expansion in the CA...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Xiaofeng A Su Catherine H Freudenreich

CAG/CTG repeats are structure-forming repetitive DNA sequences, and expansion beyond a threshold of ∼35 CAG repeats is the cause of several human diseases. Expanded CAG repeats are prone to breakage, and repair of the breaks can cause repeat contractions and expansions. In this study, we found that cotranscriptional R-loops formed at a CAG-70 repeat inserted into a yeast chromosome. R-loops wer...

Journal: :Human molecular genetics 1997
Y Takiyama K Sakoe M Soutome M Namekawa T Ogawa I Nakano S Igarashi M Oyake H Tanaka S Tsuji M Nishizawa

To investigate the mechanism of the meiotic instability of expanded CAG repeats in the gene for Machado-Joseph disease (MJD1), we analyzed the CAG repeat sizes of 1036 single sperm from six individuals with Machado-Joseph disease (MJD). The segregation ratio between single sperm with an expanded allele and those with a normal allele is significantly different (P <0.0001) from the expected 1:1 s...

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...

2016
Chung Lyul Lee Jaegeun Lee Yong Gil Na Ki Hak Song

We evaluated whether type III 5-alpha reductase (SRD5A3; steroid reductase 5-alpha 3) polymorphism was associated with susceptibility of benign prostate hyperplasia (BPH) and the combined effects in BPH risk between the type of short tandem repeat (STR) in SRD5A3 and the length of trinucleotide (CAG) repeats in androgen receptor (AR) gene. We compared the length of AC repeats in STR region of S...

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