(Q38353574)

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GALNT3, a gene associated with hyperphosphatemic familial tumoral calcinosis, is transcriptionally regulated by extracellular phosphate and modulates matrix metalloproteinase activity

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scholarly article

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Europe PubMed Central

PMC publication ID

2 September 2017

GALNT3, a gene associated with hyperphosphatemic familial tumoral calcinosis, is transcriptionally regulated by extracellular phosphate and modulates matrix metalloproteinase activity (English)

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

extracellular matrix

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hyperphosphatemic familial tumoral calcinosis

0 references

4

object named as

Jouni Uitto

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

author name string

Ilana Chefetz

1

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

Kimitoshi Kohno

2

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

Hiroto Izumi

3

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

Gabriele Richard

5

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

Eli Sprecher

6

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Europe PubMed Central

PMC publication ID

2 September 2017

language of work or name

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publication date

11 October 2008

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

Biochimica et Biophysica Acta

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Europe PubMed Central

PMC publication ID

2 September 2017

1792

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

1

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

61-67

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

A novel missense mutation in GALNT3 causing hyperostosis-hyperphosphataemia syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Physiological regulation and disorders of phosphate metabolism--pivotal role of fibroblast growth factor 23

1 reference

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6 September 2017

Calcium and phosphate homeostasis: concerted interplay of new regulators

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Hyperphosphatemia: effects on bone metabolism and cardiovascular risk.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Osteopontin: a multifunctional molecule regulating chronic inflammation and vascular disease

1 reference

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6 September 2017

A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Role of fibroblast growth factor 23 in phosphate homeostasis and pathogenesis of disordered mineral metabolism in chronic kidney disease.

1 reference

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6 September 2017

Phosphorus homeostasis in normal health and in chronic kidney disease patients with special emphasis on dietary phosphorus intake

1 reference

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6 September 2017

Phosphate metabolism in the setting of chronic kidney disease: significance and recommendations for treatment

1 reference

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6 September 2017

Osteogenic responses in fibroblasts activated by elastin degradation products and transforming growth factor-beta1: role of myofibroblasts in vascular calcification

1 reference

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6 September 2017

Tumoral calcinosis: new insights for the rheumatologist into a familial crystal deposition disease

1 reference

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6 September 2017

Two novel nonsense mutations in GALNT3 gene are responsible for familial tumoral calcinosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Hyperostosis-hyperphosphatemia syndrome: a congenital disorder of O-glycosylation associated with augmented processing of fibroblast growth factor 23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Klotho converts canonical FGF receptor into a specific receptor for FGF23

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Tumoral calcinosis presenting with eyelid calcifications due to novel missense mutations in the glycosyl transferase domain of the GALNT3 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Polypeptide GalNAc-transferase T3 and familial tumoral calcinosis. Secretion of fibroblast growth factor 23 requires O-glycosylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Mendelian disorders deserve more attention

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

The roles of specific genes implicated as circulating factors involved in normal and disordered phosphate homeostasis: frizzled related protein-4, matrix extracellular phosphoglycoprotein, and fibroblast growth factor 23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Calcinosis in rheumatic diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

FGF23 and disorders of phosphate homeostasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Keratinocyte growth factor: effects on keratinocytes and mechanisms of action

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

All in the family: the UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Human fibroblast growth factor-23 mutants suppress Na+-dependent phosphate co-transport activity and 1alpha,25-dihydroxyvitamin D3 production

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

N-acetylgalactosaminyl transferase-3 is a potential new marker for non-small cell lung cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

The interplay of matrix metalloproteinases, morphogens and growth factors is necessary for branching of mammary epithelial cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Basic calcium phosphate crystals induce synthesis and secretion of 92 kDa gelatinase (gelatinase B/matrix metalloprotease 9) in human fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Extension of life-span by introduction of telomerase into normal human cells

1 reference

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6 September 2017

cDNA cloning and expression of a novel human UDP-N-acetyl-alpha-D-galactosamine. Polypeptide N-acetylgalactosaminyltransferase, GalNAc-t3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Hyperphosphatemic familial tumoral calcinosis caused by a mutation in GALNT3 in a European kindred

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

6 September 2017

Tumoral calcinosis revisited--common and uncommon features. Report of ten cases and review

1 reference

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14 September 2017

Degradation of the Alzheimer disease amyloid beta-peptide by metal-dependent up-regulation of metalloprotease activity

1 reference

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14 September 2017

Fibroblast growth factor-23 mutants causing familial tumoral calcinosis are differentially processed.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

14 September 2017

An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

14 September 2017

Fibroblast growth factor 7: an inhibitor of phosphate transport derived from oncogenic osteomalacia-causing tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

14 September 2017

Src/ERK but not phospholipase D is involved in keratinocyte growth factor-stimulated secretion of matrix metalloprotease-9 and urokinase-type plasminogen activator in SNU-16 human stomach cancer cell

1 reference

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14 September 2017

FGF7/KGF triggers cell transformation and invasion on immortalised human prostatic epithelial PNT1A cells.

1 reference

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27 September 2017

Regulation of the expression of stromelysin-2 by growth factors in keratinocytes: implications for normal and impaired wound healing

1 reference

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23 June 2018

Sequential activation of matrix metalloproteinase 9 and transforming growth factor beta in arterial elastocalcinosis

1 reference

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31 August 2018

Mechanism of basic calcium phosphate crystal-stimulated matrix metalloproteinase-13 expression by osteoarthritic synovial fibroblasts: inhibition by prostaglandin E2.

1 reference

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31 August 2018

The role of mutant UDP-N-acetyl-alpha-D-galactosamine-polypeptide N-acetylgalactosaminyltransferase 3 in regulating serum intact fibroblast growth factor 23 and matrix extracellular phosphoglycoprotein in heritable tumoral calcinosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

Changes in serum calcium, phosphate, and PTH and the risk of death in incident dialysis patients: a longitudinal study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

Familial tumoral calcinosis and testicular microlithiasis associated with a new mutation of GALNT3 in a white family.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

Role of serum fetuin-A, a major inhibitor of systemic calcification, in pseudoxanthoma elasticum.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

Relation between serum phosphate level and cardiovascular event rate in people with coronary disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

A novel mutation in fibroblast growth factor 23 gene as a cause of tumoral calcinosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

A novel GALNT3 mutation in a pseudoautosomal dominant form of tumoral calcinosis: evidence that the disorder is autosomal recessive

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

Induction of matrix metalloproteinase-8 in human fibroblasts by basic calcium phosphate and calcium pyrophosphate dihydrate crystals: effect of phosphocitrate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

Basic calcium phosphate crystals up-regulate metalloproteinases but down-regulate tissue inhibitor of metalloproteinase-1 and -2 in human fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3169302

31 August 2018

Elevated serum calcitriol concentrations do not fall in response to hyperphosphatemia in familial tumoral calcinosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phosphonocarboxylic acids as specific inhibitors of Na+-dependent transport of phosphate across renal brush border membrane

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial tumoral calcinosis. A clinical, histopathologic, and ultrastructural study with an analysis of its calcifying process and pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bisphosphonates and tetracycline: experimental models for their evaluation in calcium-related disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel recessive mutation in fibroblast growth factor-23 causes familial tumoral calcinosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of intraepidermal glycosyltransferase ppGalNac-T3 expression in familial tumoral calcinosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Matrix metalloproteinase inhibition attenuates aortic calcification

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SPP1 promoter polymorphisms: identification of the first modifier gene for pseudoxanthoma elasticum

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NovelGALNT3Mutations Causing Hyperostosis-Hyperphosphatemia Syndrome Result in Low Intact Fibroblast Growth Factor 23 Concentrations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aberrant mineralization of connective tissues in a mouse model of pseudoxanthoma elasticum: systemic and local regulatory factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two novel GALNT3 mutations in familial tumoral calcinosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A homozygous missense mutation in human KLOTHO causes severe tumoral calcinosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural basis for the regulation of UDP-N-acetyl-alpha-D-galactosamine: polypeptide N-acetylgalactosaminyl transferase-3 gene expression in adenocarcinoma cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inorganic phosphate induces apoptosis of osteoblast-like cells in culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/18976705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.BBADIS.2008.09.016

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

2 September 2017

ResearchGate publication ID

0 references

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