(Q54749620)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18059085%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency (English)

1 reference

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29 December 2019

8

1 reference

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29 December 2019

author name string

Thiti Snabboon

1

1 reference

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29 December 2019

Wanee Plengpanich

2

1 reference

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29 December 2019

Patinat Buranasupkajorn

3

1 reference

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29 December 2019

Ratchada Khwanjaipanich

4

1 reference

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29 December 2019

Padiporn Vasinanukorn

5

1 reference

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29 December 2019

Sompongse Suwanwalaikorn

6

1 reference

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29 December 2019

Weerapan Khovidhunkit

7

1 reference

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29 December 2019

publication date

4 December 2007

1 reference

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29 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18059085%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

volume

69

1 reference

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29 December 2019

issue

1

1 reference

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29 December 2019

page(s)

60-64

1 reference

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Pituitary development: regulatory codes in mammalian organogenesis

29 December 2019

cites work

1 reference

Molecular basis of combined pituitary hormone deficiencies

21 January 2018

1 reference

Novel insights into the aetiology and pathogenesis of hypopituitarism

21 January 2018

1 reference

Characterization of the gene encoding human pituitary-specific transcription factor, Pit-1

21 January 2018

1 reference

Signaling and transcriptional mechanisms in pituitary development

21 January 2018

1 reference

POU domain factors in the neuroendocrine system: lessons from developmental biology provide insights into human disease

21 January 2018

1 reference

Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1.

21 January 2018

1 reference

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

21 January 2018

1 reference

New N-terminal located mutation (Q4ter) within the POU1F1-gene (PIT-1) causes recessive combined pituitary hormone deficiency and variable phenotype

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000111797

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18059085%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference