(Q60021568)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9920407%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

title

Disorders of the calcium-sensing receptor (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9920407%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9920407%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

author name string

R.V. Thakker

series ordinal

1

0 references

publication date

1 December 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9920407%20AND%20SRC:MED&resulttype=core&format=json

Biochimica et Biophysica Acta

9 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9920407%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

volume

1448

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9 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9920407%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

page(s)

166-170

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9920407%20AND%20SRC:MED&resulttype=core&format=json

Mutations in the calcium-sensing receptor and their clinical implications

9 December 2019

cites work

1 reference

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7 January 2021

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation

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https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

The hypocalciuric or benign variant of familial hypercalcemia: clinical and biochemical features in fifteen kindreds

1 reference

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7 January 2021

Familial benign hypercalcaemia

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7 January 2021

Familial benign hypercalcemia (hypocalciuric hypercalcemia). Clinical and pathogenetic studies in 21 families

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7 January 2021

Significant developmental elevation in serum parathyroid hormone levels in a large kindred with familial benign (hypocalciuric) hypercalcemia

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7 January 2021

NEONATAL FAMILIAL PRIMARY HYPERPARATHYROIDISM

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7 January 2021

An association between neonatal severe primary hyperparathyroidism and familial hypocalciuric hypercalcemia in three kindreds

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7 January 2021

Altered parathyroid set point to calcium in familial hypocalciuric hypercalcaemia

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7 January 2021

Cloning and characterization of an extracellular Ca(2+)-sensing receptor from bovine parathyroid

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7 January 2021

Cloning, expression, and gene structure of a G protein-coupled glutamate receptor from rat brain

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7 January 2021

Cloning and functional expression of a rat kidney extracellular calcium/polyvalent cation-sensing receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

Calcium sensing receptor: molecular cloning in rat and localization to nerve terminals

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https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

Molecular cloning and functional expression of human parathyroid calcium receptor cDNAs

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

Mapping of the calcium-sensing receptor gene (CASR) to human chromosome 3q13.3-21 by fluorescence in situ hybridization, and localization to rat chromosome 11 and mouse chromosome 16.

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

Preliminary localization of a gene for autosomal dominant hypoparathyroidism to chromosome 3q13

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

Mutations in the Ca(2+)-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism

1 reference

https://api.crossref.org/works/10.1016%2FS0167-4889%2898%2900140-2

7 January 2021

10.1016/S0167-4889(98)00140-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9920407%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference