Mutations in PROP1 cause familial combined pituitary hormone deficiency (Q24308762)

central nervous system development

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

W Wu

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J D Cogan

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R W Pfäffle

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J S Dasen

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H Frisch

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S M O'Connell

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S E Flynn

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M R Brown

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P E Mullis

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J S Parks

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J A Phillips

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M G Rosenfeld

Pituitary lineage determination by the Prophet of Pit-1 homeodomain factor defective in Ames dwarfism

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language of work or name

English

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publication date

February 1998

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147-9

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

Ames dwarf mice exhibit somatotrope commitment but lack growth hormone-releasing factor response

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

The Ames dwarf gene is required for Pit-1 gene activation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

Gonadotropin secretion, synthesis, and gene expression in human growth hormone transgenic mice and in Ames dwarf mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

Genetic mapping of the human pituitary-specific transcriptional factor gene and its analysis in familial panhypopituitary dwarfism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

7 January 2021

The response of two types of dwarf mice to growth hormone, thyrotropin, and thyroxine

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

7 January 2021

Localization of the panhypopituitary dwarf mutation (df) on mouse chromosome 11 in an intersubspecific backcross

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

7 January 2021

Early evolutionary origin of major homeodomain sequence classes

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

7 January 2021

Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

7 January 2021

Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0298-147

7 January 2021

Identifiers

DOI

10.1038/NG0298-147

1 reference

Consolidated OpenCitations Corpus – April 2017

Dimensions Publication ID

1030737601

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Fatcat ID

release_bjlkuppr7jeqbk4astv6sxexwe

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1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

9462743

1 reference

Consolidated OpenCitations Corpus – April 2017