(Q24290481)

phosphate ion homeostasis

GOA release 2020-03-11

1 reference

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

GOA release 2020-03-11

language of work or name

English

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publication date

November 2000

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published in

Nature Genetics

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volume

26

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page(s)

345-8

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issue

3

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cites work

1 reference

7 January 2021

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

1 reference

7 January 2021

Hereditary hypophosphatemic rickets with hypercalciuria

1 reference

7 January 2021

Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p13.

1 reference

7 January 2021

Fibroblast growth factor receptor 3 is a negative regulator of bone growth

1 reference

7 January 2021

Abnormal bone growth and selective translational regulation in basic fibroblast growth factor (FGF-2) transgenic mice

1 reference

7 January 2021

Fgf-10 is required for both limb and lung development and exhibits striking functional similarity to Drosophila branchless

1 reference

7 January 2021

An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination

1 reference

7 January 2021

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

1 reference

7 January 2021

A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

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7 January 2021

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

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7 January 2021

FGFR activation in skeletal disorders: too much of a good thing

1 reference

7 January 2021

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

1 reference

7 January 2021

Tumor-induced osteomalacia--unveiling a new hormone

1 reference

7 January 2021

Development of enzyme-linked immunosorbent assay for acidic fibroblast growth factor and its clinical application

1 reference

7 January 2021

Three DNA markers for hypophosphataemic rickets

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7 January 2021

Prediction of complete gene structures in human genomic DNA

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7 January 2021

Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

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7 January 2021

Identification of protein coding regions in the human genome by quadratic discriminant analysis

1 reference

7 January 2021

Reexpression of cartilage-specific genes by dedifferentiated human articular chondrocytes cultured in alginate beads

1 reference

7 January 2021

Identifiers

DOI

10.1038/81664

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

150769

1050621705

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150769

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference