Literature DB >> 14526179

SCA10 and ATTCT repeat expansion: clinical features and molecular aspects.

X Lin1, T Ashizawa.   

Abstract

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Year:  2003        PMID： 14526179     DOI： 10.1159/000072853

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN： 1424-8581            Impact factor:   1.636


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  12 in total

Review 1.  Neurodegeneration the RNA way.

Authors:  Abigail J Renoux; Peter K Todd
Journal:  Prog Neurobiol       Date:  2011-11-03       Impact factor: 11.685

2.  Expansions, contractions, and fragility of the spinocerebellar ataxia type 10 pentanucleotide repeat in yeast.

Authors:  Nicole Cherng; Alexander A Shishkin; Lucas I Schlager; Ryan H Tuck; Laura Sloan; Robert Matera; Partha S Sarkar; Tetsuo Ashizawa; Catherine H Freudenreich; Sergei M Mirkin
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-31       Impact factor: 11.205

3.  A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult.

Authors:  Katherine E Hekman; Guo-Yun Yu; Christopher D Brown; Haipeng Zhu; Xiaofei Du; Kristina Gervin; Dag Erik Undlien; April Peterson; Giovanni Stevanin; H Brent Clark; Stefan M Pulst; Thomas D Bird; Kevin P White; Christopher M Gomez
Journal:  Hum Mol Genet       Date:  2012-09-21       Impact factor: 6.150

Review 4.  Recent progress in spinocerebellar ataxia type-10 (SCA10).

Authors:  Xi Lin; Tetsuo Ashizawa
Journal:  Cerebellum       Date:  2005       Impact factor: 3.847

5.  Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10.

Authors:  Misti C White; Rui Gao; Weidong Xu; Santi M Mandal; Jung G Lim; Tapas K Hazra; Maki Wakamiya; Sharon F Edwards; Salmo Raskin; Hélio A G Teive; Huda Y Zoghbi; Partha S Sarkar; Tetsuo Ashizawa
Journal:  PLoS Genet       Date:  2010-06-10       Impact factor: 5.917

6.  Unstable spinocerebellar ataxia type 10 (ATTCT*(AGAAT) repeats are associated with aberrant replication at the ATX10 locus and replication origin-dependent expansion at an ectopic site in human cells.

Authors:  Guoqi Liu; John J Bissler; Richard R Sinden; Michael Leffak
Journal:  Mol Cell Biol       Date:  2007-09-10       Impact factor: 4.272

Review 7.  Advances in mechanisms of genetic instability related to hereditary neurological diseases.

Authors:  Robert D Wells; Ruhee Dere; Micheal L Hebert; Marek Napierala; Leslie S Son
Journal:  Nucleic Acids Res       Date:  2005-07-08       Impact factor: 16.971

8.  Computational Investigation of Bending Properties of RNA AUUCU, CCUG, CAG, and CUG Repeat Expansions Associated With Neuromuscular Disorders.

Authors:  Amirhossein Taghavi; Ilyas Yildirim
Journal:  Front Mol Biosci       Date:  2022-04-11

Review 9.  Transgenic models of spinocerebellar ataxia type 10: modeling a repeat expansion disorder.

Authors:  Karen N McFarland; Tetsuo Ashizawa
Journal:  Genes (Basel)       Date:  2012-07-30       Impact factor: 4.141

Review 10.  Molecular Mechanisms in Pentanucleotide Repeat Diseases.

Authors:  Joana R Loureiro; Ana F Castro; Ana S Figueiredo; Isabel Silveira
Journal:  Cells       Date:  2022-01-08       Impact factor: 6.600
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