About 3% of the human genome is composed of simple sequence repeats and many of these sequences occur within genes. These repeats are often polymorphic in a normal population and their expansion in specific genes leads to a number of hereditary neurological diseases. Normal variants of disease-relat
โฆ LIBER โฆ
Evolutionary scenario for acquisition of CAG repeats in human SCA1 gene
โ Scribed by Tatsuaki Kurosaki; Aya Ninokata; Li Wang; Shintaroh Ueda
- Book ID
- 116507434
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 684 KB
- Volume
- 373
- Category
- Article
- ISSN
- 0378-1119
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Patterns of CAG repeat interruptions in
โ
Krzysztof Sobczak; Wlodzimierz J. Krzyzosiak
๐
Article
๐
2004
๐
John Wiley and Sons
๐
English
โ 346 KB
Comparative studies of the CAG repeats i
โ
Limprasert, Pornprot; Nouri, Nassim; Nopparatana, Chamnong; Deininger, Prescott
๐
Article
๐
1997
๐
John Wiley and Sons
๐
English
โ 42 KB
๐ 2 views
The CAG repeat tract at the autosomal dominant spinocerebellar ataxia type 1 (SCA1) locus was analyzed in SCA1 families and French-Acadian, African-American, Caucasian, Greenland Inuit, and Thai populations. The normal alleles had 9-37 repeats, whereas disease alleles contained 44-64 repeats. The CA
Unexpected clinicopathological phenotype
โ
T. Uchihara; Y. Takeda; T. Kobayashi; T. Kasuga; K. Ishikawa; K. Kirei; H. Mizus
๐
Article
๐
2005
๐
Springer
๐
English
โ 204 KB
Spinocerebellar ataxia 1 (SCA1) in the J
โ
Yoshihiro Suzuki; Hidenao Sasaki; Akemi Wakisaka; Akio Takada; Takashi Yoshiki;
๐
Article
๐
1995
๐
Nature Publishing Group
๐
English
โ 920 KB
Minimum CAG repeat in the human calmodul
โ
Sonja L. Toutenhoofd; Fabiana Garcia; David A. Zacharias; Rebecca A. Wilson; Ema
๐
Article
๐
1998
๐
Elsevier Science
๐
English
โ 258 KB
Studying human mutations by sperm typing
โ
Zhang, Lin; Leeflang, Esther P.; Yu, Jian; Arnheim, Norman
๐
Article
๐
1994
๐
Nature Publishing Group
๐
English
โ 603 KB