Disruption of copper homeostasis due to a mutation of Atp7a delays the onset of prion disease

ZBTB1 is a determinant of lymphoid development

(2011) Owen M. Siggs et al.   JOURNAL OF EXPERIMENTAL MEDICINE

Copper(II)-Induced Secondary Structure Changes and Reduced Folding Stability of the Prion Protein

(2011) Nadine D. Younan et al.   JOURNAL OF MOLECULAR BIOLOGY

Variably Protease-Sensitive Prionopathy: a Novel Disease of the Prion Protein

(2011) Pierluigi Gambetti et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

ATP7A-related copper transport diseases—emerging concepts and future trends

(2011) Stephen G. Kaler   Nature Reviews Neurology

Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy

(2010) Marina L. Kennerson et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Mice with altered serotonin 2C receptor RNA editing display characteristics of Prader–Willi syndrome

(2010) Michael V. Morabito et al.   NEUROBIOLOGY OF DISEASE

Role of copper and manganese in prion disease progression

(2009) Gerda Mitteregger et al.   BRAIN RESEARCH

Early Onset Prion Disease from Octarepeat Expansion Correlates with Copper Binding Properties

(2009) Daniel J. Stevens et al.   PLoS Pathogens

Copper(II) Ion Binding to Cellular Prion Protein

(2008) Jernej Zidar et al.   Journal of Chemical Information and Modeling