Prions may channel RNA's messages
Prions get mostly bad press, but they may be the keys to controlling protein synthesis in cells.
Prions get mostly bad press, but they may be the keys to controlling protein synthesis in cells.
Molecular & Computational biology
Nov 15, 2021
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292
In a study published in Science Advances, researchers from the Federal University of Rio de Janeiro (UFRJ) and the German Center for Neurodegenerative Diseases (DZNE-Berlin) shed light on the intricate dance between the prion ...
Molecular & Computational biology
Dec 1, 2023
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52
The highest-ever resolution imaging of an infectious prion provides the first atomic-level data of how these abnormal proteins are assembled to cause fatal neurodegenerative diseases in people and animals—and how they can ...
Molecular & Computational biology
Aug 23, 2021
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147
Many plants and trees flower in the spring when it gets warmer. How plants sense Scientists from the UK, France, Korea and Germany focused on a protein called EARLY FLOWERING3 (ELF3). ELF3 is a key part of the circadian clock ...
Plants & Animals
Aug 27, 2020
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21
A short segment of an infectious protein known as a prion protein plays a crucial role in determining how susceptible the protein is to interspecies prion transmission, RIKEN researchers have discovered in a yeast study. ...
Cell & Microbiology
Jul 17, 2020
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31
A molecular biologist at the University of Massachusetts Amherst who has for decades studied the nightmarish group of fatal diseases caused by prions—chronic wasting disease in deer, mad cow in cattle and its human analog—credits ...
Molecular & Computational biology
May 6, 2020
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162
Scientists at the Stowers Institute for Medical Research have identified a physical basis for the spread of corrupted proteins known as prions inside cells. Their research findings are reported in the July 5, 2018, issue ...
Cell & Microbiology
Jul 5, 2018
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122
Prions are self-propagating protein aggregates that can be transmitted between cells. The aggregates are associated with human diseases. Indeed, pathological prions cause mad cow disease and in humans Creutzfeldt-Jakob disease. ...
Cell & Microbiology
Jan 9, 2018
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126
Researchers studying a protein that causes a hereditary degenerative brain disease in humans have discovered that the human, mouse and hamster forms of the protein, which have nearly identical amino acid sequences, exhibit ...
Biochemistry
Nov 6, 2017
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11
Prion diseases are scary, incurable and fatal. They first gained notoriety when cows became infected by prion proteins and, in turn, infected people. Fervor surrounding mad cow disease resulted in the U.S. banning imports ...
Biochemistry
Mar 20, 2017
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11
More reference expression data
PRNP (PRioN Protein (Creutzfeld-Jakob disease, Gerstmann-Sträussler-Scheinker syndrome, fatal familial insomnia)) is a gene that codes for a protein called the prion protein (PrP), which is expressed in the brain and several other tissues.
The human PRNP gene is located on the short (p) arm of chromosome 20 between the end (terminus) of the arm and position 12, from base pair 4,615,068 to base pair 4,630,233.
PRNP has also recently been designated CD230 (cluster of differentiation 230).
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