Researchers in Singapore have developed a new protein that can alter DNA in living cells with much higher precision than current methods.
Biochemistry
Sep 13, 2016
0
203
University of Oregon scientists have uncovered new clues to the genetic basis for scoliosis, an abnormal curvature of the spine.
Cell & Microbiology
Feb 3, 2023
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228
Researchers have used gene editing to reverse symptoms in dogs of Duchenne muscular dystrophy (DMD)—a muscle-wasting and life-shortening disease that affects one in 5,000 baby boys.
Biotechnology
Jul 25, 2017
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386
Revealing another part of the story of muscle development, Johns Hopkins researchers have shown how the cytoskeleton from one muscle cell builds finger-like projections that invade into another muscle cell's territory, eventually ...
Cell & Microbiology
Jun 4, 2011
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0
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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0
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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0
(PhysOrg.com) -- Chemists at the University at Buffalo have used rational drug design to synthesize small, cell-permeable molecules that are effective in vitro against two common types of myotonic muscular dystrophy, a result ...
Biochemistry
Aug 7, 2009
0
0
Many scientists use animals to model human diseases. Mice can be obese or display symptoms of Parkinson's disease. Rats get Alzheimer's and diabetes.
Cell & Microbiology
Jun 27, 2013
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0
Researchers from the University of Minnesota's Lillehei Heart Institute have effectively treated muscular dystrophy in mice using human stem cells derived from a new process that – for the first time – makes the ...
Cell & Microbiology
May 4, 2012
0
0
A research study has shed new light on how congenital muscular dystrophies such as Walker-Warburg syndrome progress, bringing hope for better understanding, early diagnosis and treatments of these fatal disorders.
Molecular & Computational biology
Mar 10, 2023
0
233
