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Inside Precision Medicine
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Timberlyne Therapeutics Launched Last Week with a $180 Million Series A…
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Molecular Dx
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FDA Clears Solid Biosciences Neurodegeneration Gene Therapy IND
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Posts by Anjali A. Sarkar, PhD
Anjali A. Sarkar, PhD
50 POSTS
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News & Features
Ongoing Battle Against COVID-19 Aided by Variant Tracking, Better Understanding of...
May 10, 2021
News & Features
Triplet’s ASO Huntington’s Disease Candidate Has Potential to Treat Other Repeat...
April 28, 2021
Molecular Dx
More than 500 Structural Variants Linked to Hereditary Cancer and Cardiovascular...
April 26, 2021
Molecular Dx
Genetics of Major Psychiatric Disorders Differ Significantly Between Sexes
March 25, 2021
Molecular Dx
Clopidogrel (Plavix) is a Safe and Effective Blood Thinner in Patients...
March 19, 2021
News & Features
Rutgers Researchers Reveal New Approach to Genome Editing
February 24, 2021
News & Features
Drug That Enables Consistent p53 Signaling May Improve Radiation Therapy for...
February 17, 2021
News & Features
AI Roots out Lung Cancer Patients at Risk of Hyperprogression from...
February 9, 2021
Molecular Dx
Human Genome Project at 20
February 8, 2021
News & Features
Metabolomic Shift from Hormone Therapy Increases Coronary Heart Disease Risk in...
December 18, 2020
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Inside Precision Medicine
![A new technique to cheaply and rapidly create sets of DNA fragments that include all possible genetic variants will help scientists distinguish between genetic variants linked to disease and those that are innocuous. [Michael Worful]](https://www.insideprecisionmedicine.com/wp-content/uploads/2019/01/820-324x160.jpeg "More than 500 Structural Variants Linked to Hereditary Cancer and Cardiovascular Disorders Identified")
