Transcription factors regulating pituitary development (Q28146190)

Europe PubMed Central

title

Transcription factors regulating pituitary development (English)

1 reference

https://doi.org/10.1016%2FS1096-6374%2899%2980074-4

14 April 2017

author name string

J S Parks

1

0 references

M R Brown

2

0 references

John S. Parks

1

1 reference

https://doi.org/10.1016%2FS1096-6374%2899%2980074-4

14 April 2017

Milton R. Brown

2

1 reference

https://doi.org/10.1016%2FS1096-6374%2899%2980074-4

14 April 2017

language of work or name

English

0 references

publication date

June 1999

1 reference

https://doi.org/10.1016%2FS1096-6374%2899%2980074-4

Growth Hormone & I G F Research

14 April 2017

published in

1 reference

https://doi.org/10.1016%2FS1096-6374%2899%2980074-4

14 April 2017

volume

9 Suppl B

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9

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https://doi.org/10.1016%2FS1096-6374%2899%2980074-4

14 April 2017

page(s)

2-8; discussion 8-11

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2-11

1 reference

https://doi.org/10.1016%2FS1096-6374%2899%2980074-4

The Ames dwarf gene, df, is required early in pituitary ontogeny for the extinction of Rpx transcription and initiation of lineage-specific cell proliferation

14 April 2017

cites work

1 reference

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Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

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7 January 2021

The endocrine spectrum of septo-optic dysplasia

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Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation.

1 reference

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7 January 2021

The PTX family of homeodomain transcription factors during pituitary developments.

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Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

The POU domain: a large conserved region in the mammalian pit-1, oct-1, oct-2, and Caenorhabditis elegans unc-86 gene products

1 reference

https://api.crossref.org/works/10.1016%2FS1096-6374%2899%2980074-4

7 January 2021

The pituitary-specific transcription factor GHF-1 is a homeobox-containing protein

1 reference

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7 January 2021

The POU-specific domain of Pit-1 is essential for sequence-specific, high affinity DNA binding and DNA-dependent Pit-1-Pit-1 interactions

1 reference

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7 January 2021

Function of the conserved Pit-1 gene distal enhancer in progenitor and differentiated pituitary cells

1 reference

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene

1 reference

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7 January 2021

Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiency

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7 January 2021

Mutations in the Pit-1 gene in children with combined pituitary hormone deficiency

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7 January 2021

Role of Pit-1 in the gene expression of growth hormone, prolactin, and thyrotropin

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7 January 2021

A mutation in the POU-homeodomain of Pit-1 responsible for combined pituitary hormone deficiency

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7 January 2021

Mutations in PROP1 cause familial combined pituitary hormone deficiency

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7 January 2021

A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency

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7 January 2021

Compound heterozygous deletion of the PROP-1 gene in children with combined pituitary hormone deficiency

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7 January 2021

The PROP1 2-base pair deletion is a common cause of combined pituitary hormone deficiency

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7 January 2021

Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene

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7 January 2021

The prenatal role of thyroid hormone evidenced by fetomaternal Pit-1 deficiency

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7 January 2021

Familial dwarfism: case report

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7 January 2021

Familial Hypopituitarism with Large Sella Turcica

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7 January 2021

Familial hypopituitarism associated with an enlarged pituitary fossa and an empty sella

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7 January 2021

Phenotypic Variability in Familial Combined Pituitary Hormone Deficiency Caused by a PROP1 Gene Mutation Resulting in the Substitution of Arg->Cys at Codon 120 (R120C)

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7 January 2021

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Identifiers

DOI

1 reference

https://doi.org/10.1016%2FS1096-6374%2899%2980074-4