Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease.
Copper influences the pathogenesis of prion disease, but whether it is beneficial or detrimental remains controversial. Copper homeostasis is also essential for normal physiology, as highlighted by the spectrum of diseases caused by disruption of the copper transporting enzymes ATP7A and ATP7B. Here...
Main Authors: | Siggs, O, Cruite, J, Du, X, Rutschmann, S, Masliah, E, Beutler, B, Oldstone, M |
---|---|
פורמט: | Journal article |
שפה: | English |
יצא לאור: |
2012
|
פריטים דומים
פריטים דומים
-
X-linked cholestasis in mouse due to mutations of the P4-ATPase ATP11C.
מאת: Siggs, O, et al.
יצא לאור: (2011) -
Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis
מאת: Jonathon eTelianidis, et al.
יצא לאור: (2013-08-01) -
Physiological role of Prion Protein in Copper homeostasis and angiogenic mechanisms of endothelial cells
מאת: De Riccardis Lidia, et al.
יצא לאור: (2019-04-01) -
Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia
מאת: Karin Tuschl, et al.
יצא לאור: (2016-05-01) -
Prions, protein homeostasis, and phenotypic diversity
מאת: Lindquist, Susan, et al.
יצא לאור: (2010)