The common view of heredity is that all information passed down from one generation to the next is stored in an organism's DNA. But Antony Jose, associate professor of cell biology and molecular genetics at the University ...
Biotechnology
Apr 22, 2020
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6700
Researchers from the Center for Genome Engineering within the Institute for Basic Science developed a new gene-editing platform called transcription activator-like effector-linked deaminases, or TALED. TALEDs are base editors ...
Biotechnology
Apr 25, 2022
0
44
Every summer, the news reports on a bacterium called Vibrio vulnificus found in warm saltwater that causes people to get sick, or die, after they eat raw tainted shellfish or when an open wound comes in contact with seawater.
Cell & Microbiology
Jan 14, 2015
0
185
Muscle contraction and many other movement processes are controlled by the interplay between myosin and actin filaments. Two further proteins, tropomyosin and troponin, regulate how myosin binds to actin. While theoretical ...
Cell & Microbiology
Jul 19, 2012
0
1
(PhysOrg.com) -- Researchers from the University of California, Berkeley, and the University of Iowa have turned a relatively benign virus into a highly infectious form that is ideal as a carrier for gene therapy. In its ...
Feb 16, 2009
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Muscle degeneration, the most prevalent cause of frailty in hereditary diseases and aging, could be caused by a deficiency in one key enzyme in a lipid biosynthesis pathway. Researchers at the Institute of Molecular Biotechnology ...
Cell & Microbiology
Mar 20, 2023
0
190
The diagnosis of hereditary diseases and the identification of genetic fingerprints hinge on high-sensitivity DNA imaging biotechnologies. These imaging tools detect specific genes in cells using fluorophores—fluorescent ...
Biochemistry
Dec 10, 2010
0
0
Alport syndrome (AS) is a hereditary kidney disease caused by a genetic mutation leading to type IV collagen (Col4) abnormalities. Unfortunately, treatment through the correction of Col4 functionality has not yet been developed. ...
Biochemistry
Mar 9, 2018
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32
Scientists of KIT and the University of Birmingham have identified relevant new functions of a gene that plays a crucial role in Fanconi anemia, a life-threatening disease.
Biotechnology
Apr 30, 2012
0
0
Following genetic studies of deformed calves research conducted at the University of Copenhagen is able to uncover a hitherto unknown disease found among Holstein cattle. The breeding bull from which the mutation and thus ...
Plants & Animals
Sep 21, 2017
0
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