The world's first-ever detection of two faraway neutron stars colliding, causing a massive blast that rippled through the fabric of space and time, was judged the scientific breakthrough of 2017, the journal Science said ...
Astronomy
Dec 21, 2017
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794
For several years now, the CRISPR/Cas9 gene scissors have been causing a sensation in science and medicine. This new tool of molecular biology has its origins in an ancient bacterial immune system. It protects bacteria from ...
Biotechnology
Nov 25, 2022
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178
A little-studied factor known as the Little Elongation Complex (LEC) plays a critical and previously unknown role in the transcription of small nuclear RNAs (snRNA), according to a new study led by scientists at the Stowers ...
Cell & Microbiology
Aug 8, 2013
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Scientists from King's College London have announced that 16 human embryonic stem (hES) cell lines have been approved by the US National Institutes of Health (NIH) and placed on their Stem Cell Registry, making them freely ...
Cell & Microbiology
Sep 24, 2013
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A rare, small RNA turns a gene-splicing machine into a switch that controls the expression of hundreds of human genes. Howard Hughes Medical Institute Investigator and professor of Biochemistry Gideon Dreyfuss, PhD, and his ...
Cell & Microbiology
Aug 21, 2013
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2
When most genes are transcribed, the nascent RNAs they produce are not quite ready to be translated into proteins - they have to be processed first. One of those processes is called splicing, a mechanism by which non-coding ...
Cell & Microbiology
Oct 25, 2010
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0
Scientists from Tokyo Metropolitan University have discovered that a protein called platelet-derived growth factor subunit B (PDGF-B) is continuously secreted from skeletal muscle cells and helps to repair muscles by encouraging ...
Cell & Microbiology
Jan 16, 2023
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8
(Phys.org) —Much of biomedical science – both mystifying and awe-inspiring to the lay public – depends on an unwavering focus on things that can't be easily seen, like the inner-workings of cells, in order to determine ...
Cell & Microbiology
Jul 15, 2013
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0
Mutations that lead to muscle atrophy can be repaired with the gene editor CRISPR-Cas9. A team led by ECRC researcher Helena Escobar has now introduced the tool into human muscle stem cells for the first time using mRNA, ...
Molecular & Computational biology
Mar 14, 2022
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288
Reversing a protein deficiency through gene therapy can correct motor function, restore nerve signals and improve survival in mice that serve as a model for the lethal childhood disorder spinal muscular atrophy, new research ...
Biotechnology
Feb 28, 2010
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