The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Dec. 15, 2015

Filed:

Dec. 08, 2011
Applicants:

Tzu-hao Cheng, Taipei, TW;

Chia-rung Liu, Tainan, TW;

Tzu-han Wang, Taipei, TW;

Stanley N. Cohen, Stanford, CA (US);

Inventors:

Tzu-Hao Cheng, Taipei, TW;

Chia-Rung Liu, Tainan, TW;

Tzu-Han Wang, Taipei, TW;

Stanley N. Cohen, Stanford, CA (US);

Attorneys:
Primary Examiner:
Int. Cl.
CPC ...
A61K 31/70 (2006.01); C07H 21/02 (2006.01); C07H 21/04 (2006.01); A61K 31/713 (2006.01); C12N 15/113 (2010.01); A61K 51/10 (2006.01);
U.S. Cl.
CPC ...
A61K 31/713 (2013.01); C12N 15/113 (2013.01); A61K 51/10 (2013.01); A61K 51/1075 (2013.01); C12N 2310/14 (2013.01);
Abstract

Aspects of the invention include methods of selectively reducing the deleterious activity of mutant extended trinucleotide repeat containing genes in a cell, as well as compositions used in such methods. The deleterious activity (e.g., toxicity and/or dis-functionality of products encoded thereby) of a mutant extended trinucleotide repeat containing gene may be selectively reduced in a variety of different ways, e.g., by selectively decreasing SPT4 mediated transcriptional activity, by enhancing functionality of proteins encoded thereby, etc. Aspects of the invention further include assays for identifying agents that find use in methods of the invention, e.g. as summarized above. Methods and compositions of the invention find use in a variety of different applications, including the prevention or treatment of disease conditions associated with the presence of genes containing mutant extended trinucleotide repeats, such as Huntington's Disease (HD).


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