(Q28593754)

FAM20C, golgi associated secretory pathway kinase

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

amelogenesis imperfecta

1 reference

P. Vogel

1

1 reference

31 January 2017

G. M. Hansen

2

1 reference

31 January 2017

R. W. Read

3

1 reference

31 January 2017

R. B. Vance

4

1 reference

31 January 2017

M. Thiel

5

1 reference

31 January 2017

J. Liu

6

1 reference

31 January 2017

T. J. Wronski

7

1 reference

31 January 2017

D. D. Smith

8

1 reference

31 January 2017

S. Jeter-Jones

9

1 reference

31 January 2017

R. Brommage

The autosomal dominant hypophosphatemic rickets R176Q mutation in fibroblast growth factor 23 resists proteolytic cleavage and enhances in vivo biological potency

10

1 reference

31 January 2017

language of work or name

1 reference

1 November 2012

1 reference

31 January 2017

1 reference

31 January 2017

49

1 reference

31 January 2017

998–1017

1 reference

31 January 2017

6

1 reference

24 January 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

ASARM peptides: PHEX-dependent and -independent regulation of serum phosphate

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Tissue distribution and activity testing suggest a similar but not identical function of fetuin-B and fetuin-A

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Amelogenin-deficient mice display an amelogenesis imperfecta phenotype

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Dentin matrix protein 4, a novel secretory calcium-binding protein that modulates odontoblast differentiation

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Structural basis of calcification inhibition by alpha 2-HS glycoprotein/fetuin-A. Formation of colloidal calciprotein particles

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Role of the mouse ank gene in control of tissue calcification and arthritis

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Enamel defects and ameloblast-specific expression in Enam knock-out/lacz knock-in mice

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Amelotin--a Novel Secreted, Ameloblast-specific Protein

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Association of low fetuin-A (AHSG) concentrations in serum with cardiovascular mortality in patients on dialysis: a cross-sectional study

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

FAM20B is a kinase that phosphorylates xylose in the glycosaminoglycan-protein linkage region

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Spontaneous calcification of arteries and cartilage in mice lacking matrix GLA protein

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

FAM20: an evolutionarily conserved family of secreted proteins expressed in hematopoietic cells

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Dual functional roles of dentin matrix protein 1. Implications in biomineralization and gene transcription by activation of intracellular Ca2+ store

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Unknown syndrome: microcephaly, hypoplastic nose, exophthalmos, gum hyperplasia, cleft palate, low set ears, and osteosclerosis

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Regulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathway

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

The serum protein alpha 2-Heremans-Schmid glycoprotein/fetuin-A is a systemically acting inhibitor of ectopic calcification

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

The serum protein alpha2-HS glycoprotein/fetuin inhibits apatite formation in vitro and in mineralizing calvaria cells. A possible role in mineralization and calcium homeostasis

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Hypomaturation enamel defects in Klk4 knockout/LacZ knockin mice

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Osteoprotegerin: a novel secreted protein involved in the regulation of bone density

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Effect of kallikrein 4 loss on enamel mineralization: comparison with mice lacking matrix metalloproteinase 20

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Osteopontin inhibits mineral deposition and promotes regression of ectopic calcification

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Secreted kinase phosphorylates extracellular proteins that regulate biomineralization

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Inactivation of a novel FGF23 regulator, FAM20C, leads to hypophosphatemic rickets in mice

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

A missense mutation in the human liver/bone/kidney alkaline phosphatase gene causing a lethal form of hypophosphatasia

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Wnk1 kinase deficiency lowers blood pressure in mice: A gene-trap screen to identify potential targets for therapeutic intervention

21 April 2017

1 reference

https://api.crossref.org/works/10.1177/0300985812453177

Amelogenesis imperfecta: a classification and catalogue for the 21st century

21 April 2017

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Hereditary disorders of renal phosphate wasting

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Amelogenesis imperfecta: prevalence and incidence in a northern Swedish county

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

3. Protein-protein interactions of the developing enamel matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Pex/PEX tissue distribution and evidence for a deletion in the 3' region of the Pex gene in X-linked hypophosphatemic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

FGF23 is processed by proprotein convertases but not by PHEX.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Enamelysin (matrix metalloproteinase 20)-deficient mice display an amelogenesis imperfecta phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Osteopontin deficiency produces osteoclast dysfunction due to reduced CD44 surface expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

21 January 2018

Amelogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

High-resolution electron microscope study of human enamel crystallites: size, shape, and growth

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Length and shape of enamel crystals

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Supramolecular assembly of amelogenin nanospheres into birefringent microribbons

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Mutations in fam20b and xylt1 reveal that cartilage matrix controls timing of endochondral ossification by inhibiting chondrocyte maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Loss of DMP1 causes rickets and osteomalacia and identifies a role for osteocytes in mineral metabolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

The structural biology of the developing dental enamel matrix

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Phosphate: known and potential roles during development and regeneration of teeth and supporting structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Osteosclerotic bone dysplasia in siblings with a Fam20C mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Matrix macromolecules in hard tissues control the nucleation and hierarchical assembly of hydroxyapatite.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Role of phosphophoryn in dentin mineralization

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

The use of animal models to explore amelogenin variants in amelogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Concerted regulation of inorganic pyrophosphate and osteopontin by akp2, enpp1, and ank: an integrated model of the pathogenesis of mineralization disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Dentin matrix protein 1 immobilized on type I collagen fibrils facilitates apatite deposition in vitro.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Tissue-nonspecific alkaline phosphatase and plasma cell membrane glycoprotein-1 are central antagonistic regulators of bone mineralization

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Enamel formation and amelogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Nucleation and inhibition of hydroxyapatite formation by mineralized tissue proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

FGF23 concentrations vary with disease status in autosomal dominant hypophosphatemic rickets.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Chondrogenesis mediated by PPi depletion promotes spontaneous aortic calcification in NPP1-/- mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Full-length sequence, localization, and chromosomal mapping of ameloblastin. A novel tooth-specific gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Distinct roles for intrinsic osteocyte abnormalities and systemic factors in regulation of FGF23 and bone mineralization in Hyp mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Reduced plasma pyrophosphate levels in hemodialysis patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Loss-of-function ENPP1 mutations cause both generalized arterial calcification of infancy and autosomal-recessive hypophosphatemic rickets

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Functions of KLK4 and MMP-20 in dental enamel formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Altered bone development and an increase in FGF-23 expression in Enpp1(-/-) mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Bone proteins PHEX and DMP1 regulate fibroblastic growth factor Fgf23 expression in osteocytes through a common pathway involving FGF receptor (FGFR) signaling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Autosomal recessive mental retardation, deafness, ankylosis, and mild hypophosphatemia associated with a novel ANKH mutation in a consanguineous family

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Molecular determinants of extracellular matrix mineralization in bone and blood vessels

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Phenotypic diversity and revision of the nomenclature for autosomal recessive amelogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Tooth dentin defects reflect genetic disorders affecting bone mineralization

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

The emerging role of the fibroblast growth factor-23-klotho axis in renal regulation of phosphate homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Daily peritoneal administration of sodium pyrophosphate in a dialysis solution prevents the development of vascular calcification in a mouse model of uraemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Mineral induction by immobilized phosphoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Exploring the elephant: histopathology in high-throughput phenotyping of mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

RANK ligand and osteoprotegerin: paracrine regulators of bone metabolism and vascular function

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Cellular and chemical events during enamel maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Consequences for enamel development and mineralization resulting from loss of function of ameloblastin or enamelin

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Inactivation of the osteopontin gene enhances vascular calcification of matrix Gla protein-deficient mice: evidence for osteopontin as an inducible inhibitor of vascular calcification in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Pex gene deletions in Gy and Hyp mice provide mouse models for X-linked hypophosphatemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

PHEX, FGF23, DMP1 and beyond

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

α2-HS Glycoprotein/Fetuin, a Transforming Growth Factor-β/Bone Morphogenetic Protein Antagonist, Regulates Postnatal Bone Growth and Remodeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Origin of plasma alpha2HS-glycoprotein and its accumulation in bone

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Extracellular pyrophosphate metabolism and calcification in vascular smooth muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Ocular albinism and hypopigmentation defects in Slc24a5-/- mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Calcification of vascular smooth muscle cell cultures: inhibition by osteopontin

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Binding of dentin noncollagenous matrix proteins to biological mineral crystals: an atomic force microscopy study

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Expression of FAM20C in the osteogenesis and odontogenesis of mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

A mouse model expressing a truncated form of ameloblastin exhibits dental and junctional epithelium defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Serum FGF23 levels in normal and disordered phosphorus homeostasis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Physiological role of alkaline phosphatase explored in hypophosphatasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Increased circulatory level of biologically active full-length FGF-23 in patients with hypophosphatemic rickets/osteomalacia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177

Deletion of dentin matrix protein-1 leads to a partial failure of maturation of predentin into dentin, hypomineralization, and expanded cavities of pulp and root canal during postnatal tooth development

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0300985812453177