Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases

J Branco, I Al-Ramahi, L Ukani, AM Perez… - Human molecular …, 2008 - academic.oup.com
Abstract Spinocerebellar Ataxia type 1 (SCA1) and Huntington's disease (HD) are two
polyglutamine disorders caused by expansion of a CAG repeat within the coding regions of …
被引用次数：94 相关文章

Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases.

J Branco, I Al-Ramahi, L Ukani… - Human Molecular …, 2008 - search.ebscohost.com
Abstract Spinocerebellar Ataxia type 1 (SCA1) and Huntington's disease (HD) are two
polyglutamine disorders caused by expansion of a CAG repeat within the coding regions of …
[PDF] psu.edu

[PDF][PDF] Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases

J Branco, I Al-Ramahi, L Ukani, AM Perez… - Human Molecular …, 2008 - Citeseer
Spinocerebellar Ataxia type 1 (SCA1) and Huntington's disease (HD) are two polyglutamine
disorders caused by expansion of a CAG repeat within the coding regions of the Ataxin-1 …

[引用][C] Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases

J Branco, I Al-Ramahi, L Ukani, AM Pérez… - Human Molecular …, 2007 - cir.nii.ac.jp
Comparative analysis of genetic modifiers in Drosophila points to common and distinct
mechanisms of pathogenesis among polyglutamine diseases | CiNii Research CiNii 国立情報学 …

Comparative analysis of genetic modifiers in drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases

J Branco, I Al-ramahi, L Ukani, AM Pérez… - Human molecular …, 2008 - experts.umn.edu
Abstract Spinocerebellar Ataxia type 1 (SCA1) and Huntington's disease (HD) are two
polyglutamine disorders caused by expansion of a CAG repeat within the coding regions of …

Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases

J Branco, I Al-Ramahi, L Ukani, AM Perez… - Human Molecular …, 2008 - elibrary.ru
Spinocerebellar Ataxia type 1 (SCA1) and Huntingtons disease (HD) are two polyglutamine
disorders caused by expansion of a CAG repeat within the coding regions of the Ataxin-1 …
[PDF] archive.org

[PDF][PDF] Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases

J Branco, I Al-Ramahi, L Ukani, AM Perez… - Human Molecular …, 2008 - scholar.archive.org
Spinocerebellar Ataxia type 1 (SCA1) and Huntington's disease (HD) are two polyglutamine
disorders caused by expansion of a CAG repeat within the coding regions of the Ataxin-1 …

Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases.

J Branco, I Al-Ramahi, L Ukani, AM Pérez… - Human Molecular …, 2007 - europepmc.org
Spinocerebellar Ataxia type 1 (SCA1) and Huntington's disease (HD) are two polyglutamine
disorders caused by expansion of a CAG repeat within the coding regions of the Ataxin-1 …

[引用][C] Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases

J BRANCO, I AL-RAMAHI, L UKANI… - Human molecular …, 2008 - pascal-francis.inist.fr
Comparative analysis of genetic modifiers in Drosophila points to common and distinct
mechanisms of pathogenesis among polyglutamine diseases CNRS Inist Pascal-Francis CNRS …

Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases

J Branco, I Al-Ramahi, L Ukani… - Human molecular …, 2008 - pubmed.ncbi.nlm.nih.gov
Spinocerebellar Ataxia type 1 (SCA1) and Huntington's disease (HD) are two polyglutamine
disorders caused by expansion of a CAG repeat within the coding regions of the Ataxin-1 …