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Mary Grace N. Tamio

在 July 11 2022 at 11:24 PM 已編輯

Cancer drug pulls surprising double duty to treat muscular dystrophy

#cancerdrug #drugpills #musculardystrophy

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https://cn1699.com/news/cancer-drug-pulls-surprising-double-duty-treat-muscular-dystrophy

Cancer drug pulls surprising double duty to treat muscular dystrophy | CN1699
Duchenne Muscular Dystrophy (DMD) is a debilitating genetic disorder that eventually leaves patients in a wheelchair. In a new study, researchers...
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Mary Grace N. Tamio

在 February 24 2022 at 11:42 AM 已編輯

New treatment could benefit up to 45 percent of patients with Duchenne muscular dystrophy

#musculardystrophy

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https://cn1699.com/news/new-treatment-could-benefit-45-percent-patients-duchenne-muscular-dystrophy

New treatment could benefit up to 45 percent of patients with Duchenne muscular dystrophy | CN1699
Toshifumi Yokota led research to develop and test a new “cocktail” drug that may be beneficial for up to 45 per cent of patients with a common...
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Mary Grace N. Tamio

在 February 19 2022 at 12:42 PM 已編輯

Steroid treatments for Duchenne muscular dystrophy may depend on the clock

#Steroid #steroidtreatment #musculardystrophy

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https://cn1699.com/news/steroid-treatments-duchenne-muscular-dystrophy-may-depend-clock

Steroid treatments for Duchenne muscular dystrophy may depend on the clock | CN1699
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Mary Grace N. Tamio

在 January 29 2022 at 06:11 PM 已編輯

Blocking sphingolipids counteracts muscular dystrophy

#sphingolipids #musculardystrophy

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https://cn1699.com/news/blocking-sphingolipids-counteracts-muscular-dystrophy

Blocking sphingolipids counteracts muscular dystrophy | CN1699
In a new study, the group of Johan Auwerx at EPFL's School of Life Sciences has made the first connection between muscular dystrophy and...
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Mary Grace N. Tamio

在 September 21 2020 at 09:55 PM 已編輯

CRISPR gene-editing tool tweaked to tackle muscular dystrophy via RNA

#CRISPR #geneeditingtools #musculardystrophy

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https://cn1699.com/news/crispr-gene-editing-tool-tweaked-tackle-muscular-dystrophy-rna

CRISPR gene-editing tool tweaked to tackle muscular dystrophy via RNA | CN1699
Green muscle fibers with RCas9 (the therapeutic candidate for myotonic dystrophy) have eliminated their toxic RNA (red), whereas fibers lacking...
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