(Q24315110)

phosphatidylinositol phospholipase C activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

9

J G Seidman

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author name string

M R Pollak

1

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E M Brown

2

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H L Estep

3

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P N McLaine

4

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O Kifor

5

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J Park

6

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S C Hebert

7

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C E Seidman

Inositol trisphosphate and calcium signalling

8

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language of work or name

English

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publication date

November 1994

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published in

Nature Genetics

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volume

8

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issue

3

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page(s)

303-7

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG1194-303

Cloning and expression of an inwardly rectifying ATP-regulated potassium channel

20 April 2017

1 reference

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A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty

20 April 2017

1 reference

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-303

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

20 April 2017

1 reference

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Relation between intracellular Ca2+ signals and Ca(2+)-activated Cl- current in Xenopus oocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-303

Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas

21 January 2018

1 reference

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A second-generation linkage map of the human genome

21 January 2018

1 reference

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Extracellular Ca2+ sensing, regulation of parathyroid cell function, and role of Ca2+ and other ions as extracellular (first) messengers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-303

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/10.1038%2FNG1194-303

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-303

7 January 2021

Secretory dysfunction in parathyroid cells from a neonate with severe primary hyperparathyroidism

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-303

7 January 2021

Turned on to ill effect

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-303

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-303

7 January 2021

Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride cotransporter

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-303

7 January 2021