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image: Opinion: How to Use Mobile Apps for Immunohistochemistry

Opinion: How to Use Mobile Apps for Immunohistochemistry

By Alexander E. Kalyuzhny | May 25, 2018

This guide for apps comes from personal experience testing various programs aimed to improve productivity or to help with selecting reagents.

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Researchers have been using ultrasound to control brain activity, but studies in mice and guinea pigs show it also stimulates the auditory system, presenting a confounder for direct neural stimulation.

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Determining which products of advanced biotechnology are deserving of legal protections is essential to our own social architecture.

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Researchers identified thousands of immature neurons in the brain region, countering a recent result showing little, if any, signs of neurogenesis.

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Researchers develop a new technique to selectively activate neurons deep in the rodent brain, taking a step toward noninvasive brain stimulation for neurological disorders.

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image: Top Technical Advances in 2017

Top Technical Advances in 2017

By Shawna Williams | December 25, 2017

The year’s most impressive achievements include new methods to extend CRISPR editing, patch-clamp neurons hands-free, and analyze the contents of live cells.

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image: CRISPR Helps Mice Hear

CRISPR Helps Mice Hear

By Abby Olena | December 20, 2017

Researchers reduce the severity of hereditary deafness in mice with the delivery of CRISPR-Cas9 protein-RNA complexes that inactivate a mutant gene in their inner ears. 

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image: New Resource Ranks Chemical Probes for Human Proteins

New Resource Ranks Chemical Probes for Human Proteins

By Abby Olena | December 14, 2017

With many probes being seriously flawed, Probe Miner helps researchers find those that are most specific and effective for manipulating their chosen proteins.

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Chemistry Nobel goes to Jacques Dubochet, Joachim Frank, and Richard Henderson. 

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image: Nonviral CRISPR Delivery a Success

Nonviral CRISPR Delivery a Success

By Abby Olena | October 2, 2017

Researchers use gold nanoparticles to deliver CRISPR-Cas9 and correct a point mutation in a mouse model of Duchenne muscular dystrophy. 

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