نتایج جستجو برای: 40 repeats

تعداد نتایج: 356779  

Journal: :Intractable & rare diseases research 2014
Reymundo Lozano Carolina Alba Rosero Randi J Hagerman

The fragile X mental retardation 1 gene (FMR1), which codes for the fragile X mental retardation 1 protein (FMRP), is located at Xp27.3. The normal allele of the FMR1 gene typically has 5 to 40 CGG repeats in the 5' untranslated region; abnormal alleles of dynamic mutations include the full mutation (> 200 CGG repeats), premutation (55-200 CGG repeats) and the gray zone mutation (45-54 CGG repe...

Journal: :Archives of neurology 2005
Valérie Biancalana Mathias Toft Isabelle Le Ber François Tison Elisabeth Scherrer Stephen Thibodeau Jean Louis Mandel Alexis Brice Matthew J Farrer Alexandra Dürr

BACKGROUND Fragile X-associated tremor/ataxia syndrome (FXTAS), a novel disorder in male carriers of premutations of the fragile X mental retardation 1 gene (FMR1), was recently described. The clinical presentation of FXTAS most closely resembles multiple system atrophy (MSA) because both disorders manifest with cerebellar ataxia, intention tremor, autonomic dysfunction, and parkinsonism. It ha...

2011
Honggang Wang Wuzhuang Sun Zhu Li Xiufang Wang Zhanjun Lv

Alu repeats or Line-1-ORF2 (ORF2) inhibit expression of the green fluorescent protein (GFP) gene when inserted downstream of this gene in the vector pEGFP-C1. In this work, we studied cis-acting elements that eliminated the repression of GFP gene expression induced by Alu and ORF2 and sequence characteristics of these elements. We found that sense and antisense PolyA of simian virus 40 (SV40Pol...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Mingchen Chen Peter G Wolynes

Huntington's disease (HD) is a neurodegenerative disease caused by an abnormal expansion in the polyglutamine (polyQ) track of the Huntingtin (HTT) protein. The severity of the disease depends on the polyQ repeat length, arising only in patients with proteins having 36 repeats or more. Previous studies have shown that the aggregation of N-terminal fragments (encoded by HTT exon 1) underlies the...

2004
Harumi Yamagata Mika Hayashi-Tsugane Saori Hijishita Masaki Fujisawa Michie Shibata Yukiyo Ito Mari Nakamura Miyuki Sakaguchi Rie Yoshihara Harumi Kobayashi Kazue Ito Wataru Karasawa Mayu Yamamoto Shoko Saji Satoshi Katagiri Hiroyuki Kanamori Nobukazu Namiki Yuichi Katayose Takashi Matsumoto Takuji Sasaki

Understanding the organization of eukaryotic centromeres has both fundamental and applied importance because of their roles in chromosome segregation, karyotypic stability, and artificial chromosome-based cloning and expression vectors. Using clone-by-clone sequencing methodology, we obtained the complete genomic sequence of the centromeric region of rice (Oryza sativa) chromosome 8. Analysis o...

Journal: :molecular biology research communications 2015
mahmoud houshyarfard hamid rouhani mahrokh falahati-rastegar saeid malekzadeh-shafaroudi esmat mahdikhani-moghaddam

out of fifty-two iranian nonaflatoxigenic strains of aspergillus flavus, which were collected from various substrates (soil and kernel) and sources (peanut, corn and pistachio), fifteen representatives were selected according to their different geographical origins (six provinces: guilan and golestan, ardebil, fars, kerman and semnan) and vegetative compatibility groups (vcgs, ir1 to ir15) for ...

Journal: :American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009
D Brocklebank J Gayán J M Andresen S A Roberts A B Young S R Snodgrass J B Penney M A Ramos-Arroyo J J Cha H D Rosas S M Hersch A Feigin S S Cherny N S Wexler D E Housman L R Cardon

The instability of the CAG repeat size of the HD gene when transmitted intergenerationally has critical implications for genetic counseling practices. In particular, CAG repeats between 27 and 35 have been the subject of debate based on small samples. To address this issue, we analyzed allelic instability in the Venezuelan HD kindreds, the largest and most informative families ascertained for H...

2015
Ju Sun Song Kyung-Ah Kim Ju-Hong Min Chang-Seok Ki Jong-Won Kim Duk Hyun Sung Byoung Joon Kim

PURPOSE Spinal and bulbar muscular atrophy (SBMA) is an X-linked motor neuron disease characterized by proximal muscle weakness, muscle atrophy, and fas-ciculation. Although SBMA is not uncommon in Korea, there is only one study reporting clinical characteristics and genotype-phenotype correlation in Korean patients. MATERIALS AND METHODS In this study, age at the onset of symptoms, the score...

Journal: :Infection and immunity 2003
Warren L Simmons Kevin Dybvig

The variable surface antigens (Vsa) of the murine respiratory pathogen Mycoplasma pulmonis are associated with the virulence of the microorganism in the lung. In strain UAB CT, the antigens consist of an N-terminal region that is combined with one of seven different C-terminal variable regions comprised of tandem repeats. M. pulmonis producing a VsaA protein with about 40 tandem repeats (R40) d...

The apoptotic protease-activating factor 1 (Apaf-1) receives the death signal in the intrinsic ormitochondrial pathway of apoptosis. Upon the releasing of cytochrome c from theintermembrane space of mitochondria and binding to Apaf-1 molecules, a heptamericapoptosome complex is formed and triggers the downstream cascade of caspases. Here, for thefirst time we present spontaneous mutations and r...

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