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image: Week in Review: April 28–May 2

Week in Review: April 28–May 2

By | May 2, 2014

Male scientists stress mice out; using SCNT to reprogram adult cells; acetate can reach mouse brain, reduce appetite; WHO sounds “post-antibiotic era” alarm

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image: Competition for CRISPR Commercialization

Competition for CRISPR Commercialization

By | May 1, 2014

Researchers stake their proprietary claim on the genome-editing technique.

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image: Cell Transplants for Heart Questioned

Cell Transplants for Heart Questioned

By | May 1, 2014

A report reveals that using bone marrow stem cells to treat heart disease is less promising than a decade of research has let on.

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image: Sharing the Wealth

Sharing the Wealth

By | May 1, 2014

From research results to electronic health records, biomedical data are becoming increasingly accessible. How can scientists best capitalize on the information deluge?

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image: The Youngest Victims

The Youngest Victims

By | May 1, 2014

Linking single-gene defects to inflammatory bowel disease in young children may help all sufferers of the illness.

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image: Rebuilding Missing Muscle

Rebuilding Missing Muscle

By | April 30, 2014

An acellular matrix can help guide stem cells to injury sites and regrow muscles in both mice and humans, a study finds.

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image: Toward Stopping MERS Spread

Toward Stopping MERS Spread

By | April 30, 2014

Independent teams culture the Middle East respiratory system coronavirus and identify human antibodies that could inform therapies.

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image: Epigenetic Effects of Mom’s Diet

Epigenetic Effects of Mom’s Diet

By | April 29, 2014

Molecular markers of a mother’s nutrition around the time of conception can be found in her child’s DNA.

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image: SCNT Picks Up Steam

SCNT Picks Up Steam

By | April 28, 2014

Study confirms that somatic cell nuclear transfer, an alternate method of creating patient-specific pluripotent stem cells, can be used to reprogram adult cells.

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image: Genetic Brain Disorder Explained

Genetic Brain Disorder Explained

By | April 25, 2014

Researchers uncover a mutation responsible for a rare neurological condition.

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