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X-linked genetic diseases

Dual CRISPR RNA Method May Help Treat Duchenne Muscular Dystrophy
Genome Editing

Dual CRISPR RNA Method May Help Treat Duchenne Muscular Dystrophy

Christina Jackson -
0
Door Busters: Entrada Therapeutics Is Engaging Inaccessible Intracellular Targets
Drug Discovery

Door Busters: Entrada Therapeutics Is Engaging Inaccessible Intracellular Targets

Jonathan D Grinstein, PhD -
20
Molecule May Help Overcome Symptoms of Duchenne Muscular Dystrophy
Drug Discovery

Molecule May Help Overcome Symptoms of Duchenne Muscular Dystrophy

Christina Jackson -
0
Search and Replace: Andrew Anzalone Details How Genome Editing Went Prime Time on “Close to the Edge”
Close to the Edge

Search and Replace: Andrew Anzalone Details How Genome Editing Went Prime Time on “Close to the Edge”

Kathy Vuksanaj -
22
Rising Star: Vega Targets Rare Blood Disorders with Antibodies
GEN Edge

Rising Star: Vega Targets Rare Blood Disorders with Antibodies

Alex Philippidis -
0
Leveraging Modern Electronics to Streamline CRISPR Workflows
Genome Editing

Leveraging Modern Electronics to Streamline CRISPR Workflows

Christina Jackson -
20
First Gene Therapy Approved for Adults with Hemophilia B
Genome Editing

First Gene Therapy Approved for Adults with Hemophilia B

John Sterling -
47
IPO Raises $175M for Prime, Developer of “Search and Replace” Gene Editing Platform
Genome Editing

IPO Raises $175M for Prime, Developer of “Search and Replace” Gene Editing Platform

Alex Philippidis -
0
Inhibition of Ion Channel May Prolong Survival of Duchenne Muscular Dystrophy in Mice
News

Inhibition of Ion Channel May Prolong Survival of Duchenne Muscular Dystrophy in Mice

Christina Jackson -
0
Hemophilia B Gene Therapy Shows Promise in Clinical Trial
Drug Discovery

Hemophilia B Gene Therapy Shows Promise in Clinical Trial

Anjali A. Sarkar, PhD -
0
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