Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluid

Brain calcification process and phenotypes according to age and sex: Lessons fromSLC20A2,PDGFB, andPDGFRBmutation carriers

(2015) Gaël Nicolas et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

A new SLC20A2 mutation identified in southern Italy family with primary familial brain calcification

(2015) Monica Gagliardi et al.   GENE

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

(2015) Andrea Legati et al.   NATURE GENETICS

Development and functions of the choroid plexus–cerebrospinal fluid system

(2015) Melody P. Lun et al.   NATURE REVIEWS NEUROSCIENCE

High levels of the type III inorganic phosphate transporter PiT1 (SLC20A1) can confer faster cell adhesion

(2014) Iben Boutrup Kongsfelt et al.   EXPERIMENTAL CELL RESEARCH

First Report of a De Novo Mutation at SLC20A2 in a Patient with Brain Calcification

(2014) J. B. Ferreira et al.   JOURNAL OF MOLECULAR NEUROSCIENCE

Novel mutation of SLC20A2 in an Italian patient presenting with migraine

(2014) Elisa Rubino et al.   JOURNAL OF NEUROLOGY

Fahr's Disease Linked to a Novel SLC20A2 Gene Mutation Manifesting with Dynamic Aphasia

(2014) Laura Brighina et al.   Neurodegenerative Diseases

Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification

(2014) Gaël Nicolas et al.   NEUROGENETICS

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

Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification

(2013) Gaël Nicolas et al.   BRAIN

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

A Japanese family with idiopathic basal ganglia calcification with novel SLC20A2 mutation presenting with late-onset hallucination and delusion

(2013) Kensaku Kasuga et al.   JOURNAL OF NEUROLOGY

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

Inorganic Phosphate Export by the Retrovirus Receptor XPR1 in Metazoans

(2013) Donatella Giovannini et al.   Cell Reports

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

Mapping of the minimal inorganic phosphate transporting unit of human PiT2 suggests a structure universal to PiT-related proteins from all kingdoms of life

(2011) Pernille Bøttger et al.   BMC BIOCHEMISTRY

Arterial Calcification in Chronic Kidney Disease: Key Roles for Calcium and Phosphate

(2011) Catherine M. Shanahan et al.   CIRCULATION RESEARCH

The emergence of phosphate as a specific signaling molecule in bone and other cell types in mammals

(2010) Solmaz Khoshniat et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Familial idiopathic basal ganglia calcification: a challenging clinical–pathological correlation

(2009) Christian Wider et al.   JOURNAL OF NEUROLOGY