Associated Papers
Synergistic activation of the human phosphate exporter XPR1 by KIDINS220 and inositol pyrophosphate.
Zuo P et al.
Nature Communications, 2025
40128258 (PubMed )
Supplement: 41467_2025_58200_MOESM1_ESM.pdf
Transport and InsP8 gating mechanisms of the human inorganic phosphate exporter XPR1.
Zhu Q et al.
Nature Communications, 2025
Pericytes in Primary Familial Brain Calcification.
Zarb Y et al.
Advances in Experimental Medicine and Biology, 2019
Microangiopathy in primary familial brain calcification: Evidence from skin biopsies.
Nicolas G et al.
Neurology. Genetics, 2017
XPR1 mutations are a rare cause of primary familial brain calcification.
Anheim M et al.
Journal of Neurology, 2016
XPR1: a Gene Linked to Primary Familial Brain Calcification Might Help Explain a Spectrum of Neuropsychiatric Disorders.
Moura DA et al.
Journal of Molecular Neuroscience : Mn, 2015
Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.
Legati A et al.
Nature Genetics, 2015
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