The Effects of the PRNP Gene on Circadian Rhythms
Fatal Familial Insomnia is a rare genetic disorder affecting about 27 families worldwide, caused by mutations in the prion protein gene PRNP. Symptoms include loss of sleep and disrupted circadian rhythms. The function of PNRP in circadian rhythms is not
Vlasac, Irma Marisela
core
PRNP Gene: Non-Coding Variability in Norwegian Tundra Reindeer (R. t. tarandus) - A Bioinformatic Approach [PDF]
A study about the PRNP Gene and variations in the intron and exon regionA study about the PRNP Gene and variations in the intron and exon ...
Jensen, Katja Margrethe
core
Odocoileus virginianus PRNP sequencing reveals AF (Q<sub>95</sub>G<sub>96</sub>/H<sub>95</sub>G<sub>96</sub>) advantage over AC (Q<sub>95</sub>G<sub>96</sub>/Q<sub>95</sub>S<sub>96</sub>) against chronic wasting disease. [PDF]
London EW +5 more
europepmc +1 more source
A rapid visual detection method for indel polymorphisms in the bovine PRNP gene based on a duplex MIRA-LFD assay. [PDF]
Xu Y +7 more
europepmc +1 more source
Early onset Alzheimer's disease with V180I variant of prion protein gene and a family history of dementia: a case report. [PDF]
Hamaguchi T +10 more
europepmc +1 more source
Old nodes, new tricks: optimized methods for chronic wasting disease prion detection in preserved retropharyngeal lymph nodes. [PDF]
Munster A +6 more
europepmc +1 more source

