Methods of screening for compounds for treating muscular dystrophy using UTRN mRNA translation regulation

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Oct 9, 2012
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Jun 20, 2008
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Jun 20, 2007

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Abstract

The present invention provides compounds and assays for the identification and validation of compounds for use in the treatment of muscular dystrophy (MD), or a form thereof, in which said compounds increase the post-transcriptional expression of a target gene (i.e., mIGF1, ITGA7, or UTRN).

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MIDCAP FINANCIAL TRUST AS AGENT	7255 WOODMONT AVE SUITE 200 BETHESDA MD 20814

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C12Q:MEASURING OR TESTING PROCESSES INVOLVING ENZYMES O....

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Inventor Name	Address	# of filed Patents	Total Citations
Friesen, Westley J	Huntingdon Valley, US	5	9
Naryshkin, Nikolai	East Brunswick, US	26	242
Patel, Meenal	Fairless Hills, US	7	71
Romfo, Charles	Easton, US	7	76
Tomizawa, Yuki	Edison, US	6	16
Welch, Ellen	Califon, US	37	313
Zhuo, Jin	Belle Mead, US	3	43

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Methods of screening for compounds for treating muscular dystrophy using UTRN mRNA translation regulation

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United States of America Patent

12143705

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