New insights into the pathogenesis of inherited phosphate wasting disorders. (Q33697498)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10423038%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

review article

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title

New insights into the pathogenesis of inherited phosphate wasting disorders (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10423038%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

1

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10 December 2019

author name string

Econs MJ

series ordinal

1

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28 July 2017

1 July 1999

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10423038%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

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10 December 2019

volume

25

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10 December 2019

issue

1

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10 December 2019

page(s)

131-135

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

10 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Neurological involvement in X-linked hypophosphataemic rickets

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Brief report: inhibition of renal phosphate transport by a tumor product in a patient with oncogenic osteomalacia

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

The Lumbar Spinal Canal in Hypophosphataemic Vitamin D-resistant Rickets

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Craniostenosis with familial vitamin-D-resistant rickets.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Mutational Analysis of PHEX Gene in X-Linked Hypophosphatemia

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https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

cDNA cloning of the murine Pex gene implicated in X-linked hypophosphatemia and evidence for expression in bone

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Effect of 1,25-dihydroxyvitamin D3 treatment on bone formation by transplanted cells from normal and X-linked hypophosphatemic mice

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Defective bone formation by transplanted Hyp mouse bone cells into normal mice

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Positional cloning of the HYP gene: a review

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Tumor-induced osteomalacia--unveiling a new hormone

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

X-Linked hypophosphatemic rickets: a disease often unknown to affected patients.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Localization of a renal sodium-phosphate cotransporter gene to human chromosome 5q35.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

An analysis of vertebrate mRNA sequences: intimations of translational control

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https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Direct demonstration of a humorally-mediated inhibition of renal phosphate transport in the Hyp mouse

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Cloning of human PEX cDNA. Expression, subcellular localization, and endopeptidase activity

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Abnormal regulation of renal 25-hydroxyvitamin D-1 alpha-hydroxylase activity in the X-linked hypophosphatemic mouse

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Serum 1,25-dihydroxyvitamin D levels in subjects with X-linked hypophosphatemic rickets and osteomalacia

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Partial deletion of both the spermine synthase gene and the Pex gene in the X-linked hypophosphatemic, gyro (Gy) mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Parabiosis suggests a humoral factor is involved in X-linked hypophosphatemia in mice

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Hemangiopericytoma-induced osteomalacia: tumor transplantation in nude mice causes hypophosphatemia and tumor extracts inhibit renal 25-hydroxyvitamin D 1-hydroxylase activity

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Renal transplantation in hypophosphatemia with vitamin D-resistant rickets.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Characteristics of tumor cell bioactivity in oncogenic osteomalacia

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Crosstransplantation of kidneys in normal and Hyp mice. Evidence that the Hyp mouse phenotype is unrelated to an intrinsic renal defect

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

The gene for X-linked hypophosphataemic rickets maps to a 200-300kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE)

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Candidate 56 and 58 kDa protein(s) responsible for mediating the renal defects in oncogenic hypophosphatemic osteomalacia

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Pex mRNA is localized in developing mouse osteoblasts and odontoblasts

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Hypophosphatemic nonrachitic bone disease: An entity distinct from X-linked hypophosphatemia in the renal defect, bone involvement, and inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Serum 1,25-Dihydroxyvitamin D Levels in Normal Subjects and in Patients with Hereditary Rickets or Bone Disease

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Renal Na(+)-phosphate cotransporter gene expression in X-linked Hyp and Gy mice

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Effect of phosphonoformic acid, dietary phosphate and the Hyp mutation on kinetically distinct phosphate transport processes in mouse kidney

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Bridging markers defining the map position of X linked hypophosphataemic rickets.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

Paraplegia due to ossification of ligamenta flava in X-linked hypophosphatemia. A case report

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

A comparison of the properties and enzymatic activities of three angiotensin processing enzymes: angiotensin converting enzyme, prolyl endopeptidase and neutral endopeptidase 24.11.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

X-linked hypophosphatemia: a search for gender, race, anticipation, or parent of origin effects on disease expression in children

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

A genetic study of familial hypophosphatemia and vitamin D resistant rickets with a review of the literature.

1 reference

https://api.crossref.org/works/10.1016%2FS8756-3282%2899%2900108-8

7 January 2021

10.1016/S8756-3282(99)00108-8

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10423038%20AND%20SRC:MED&resulttype=core&format=json

10 December 2019

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