(Q28289445)

1

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A Roy

2

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F Dastot

3

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I Ghali

4

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C Teinturier

5

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I Netchine

6

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V Cacheux

7

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M Hafez

8

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N Salah

9

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J L Chaussain

10

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M Goossens

11

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P Bougnères

12

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S Amselem

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

13

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language of work or name

English

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publication date

23 October 1998

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published in

FEBS Letters

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volume

437

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issue

3

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page(s)

216-20

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

Effects of Prolactin (PRL) on Pituitary and Testicular Function in Mice with Hereditary PRL Deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

The molecular basis of hypopituitarism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

Mutations in PROP1 cause familial combined pituitary hormone deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

Replacement of insulin receptor tyrosine residues 1162 and 1163 compromises insulin-stimulated kinase activity and uptake of 2-deoxyglucose

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

Defective membrane expression of human growth hormone (GH) receptor causes Laron-type GH insensitivity syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

Early evolutionary origin of major homeodomain sequence classes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

A catalogue of splice junction sequences

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

Gsh-1, an orphan Hox gene, is required for normal pituitary development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

Specification of pituitary cell lineages by the LIM homeobox gene Lhx3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

Multistep control of pituitary organogenesis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0014-5793%2898%2901234-4