SLC20A2 Deficiency in Mice Leads to Elevated Phosphate Levels in Cerbrospinal Fluid and Glymphatic Pathway-Associated Arteriolar Calcification, and Recapitulates Human Idiopathic Basal Ganglia Calcification

Update and Mutational Analysis ofSLC20A2: A Major Cause of Primary Familial Brain Calcification

(2015) Roberta R. Lemos et al.   HUMAN MUTATION

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export

(2015) Andrea Legati et al.   NATURE GENETICS

The Glymphatic System: A Beginner’s Guide

(2015) Nadia Aalling Jessen et al.   NEUROCHEMICAL RESEARCH

Primary familial brain calcification: update on molecular genetics

(2015) Ilaria Taglia et al.   NEUROLOGICAL SCIENCES

Choroid plexus dysfunction impairs beta-amyloid clearance in a triple transgenic mouse model of Alzheimer’s disease

(2015) Ibrahim González-Marrero et al.   Frontiers in Cellular Neuroscience

PDGF, Pericytes and the Pathogenesis of Idiopathic Basal Ganglia Calcification (IBGC)

(2014) Christer Betsholtz et al.   BRAIN PATHOLOGY

Renal phosphate transporters

(2014) Eleanor Lederer   CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION

A de novo nonsense PDGFB mutation causing idiopathic basal ganglia calcification with laryngeal dystonia

(2014) Gaël Nicolas et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

PDGFB Partial Deletion: a New, Rare Mechanism Causing Brain Calcification with Leukoencephalopathy

(2014) Gaël Nicolas et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

Evaluation of SLC20A2 mutations that cause idiopathic basal ganglia calcification in Japan

(2014) M. Yamada et al.   NEUROLOGY

Sodium-Dependent Phosphate Cotransporters and Phosphate-Induced Calcification of Vascular Smooth Muscle Cells

(2013) Matthew H. Crouthamel et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

Reporting a new mutation at the SLC20A2 gene in familial idiopathic basal ganglia calcification

(2013) R. R. Lemos et al.   EUROPEAN JOURNAL OF NEUROLOGY

Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia calcification

(2013) Wan-Jin Chen et al.   GENE

Loss of Function of Slc20a2 Associated with Familial Idiopathic Basal Ganglia Calcification in Humans Causes Brain Calcifications in Mice

(2013) Nina Jensen et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice

(2013) Annika Keller et al.   NATURE GENETICS

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

(2013) Sandy Chan Hsu et al.   NEUROGENETICS

Association between a Novel Mutation in SLC20A2 and Familial Idiopathic Basal Ganglia Calcification

(2013) Yang Zhang et al.   PLoS One

Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis

(2012) Cheng Wang et al.   NATURE GENETICS

Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification

(2012) G. Nicolas et al.   NEUROLOGY

A Paravascular Pathway Facilitates CSF Flow Through the Brain Parenchyma and the Clearance of Interstitial Solutes, Including Amyloid  

(2012) J. J. Iliff et al.   Science Translational Medicine

Smooth Muscle Cells Give Rise to Osteochondrogenic Precursors and Chondrocytes in Calcifying Arteries

(2009) Mei Y. Speer et al.   CIRCULATION RESEARCH

Chronic Mineral Dysregulation Promotes Vascular Smooth Muscle Cell Adaptation and Extracellular Matrix Calcification

(2009) R. C. Shroff et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY