(Q56535712)

1

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Anne Roy

2

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Florence Dastot

3

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Isis Ghali

4

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Cécile Teinturier

5

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Irène Netchine

6

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Valère Cacheux

7

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Mona Hafez

8

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Nermine Salah

9

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Jean-Louis Chaussain

10

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Michel Goossens

11

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Serge 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)

216-220

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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

21 January 2018

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.

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

The molecular basis of hypopituitarism

21 January 2018

1 reference

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

Mutations in PROP1 cause familial combined pituitary hormone deficiency

21 January 2018

1 reference

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

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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

A catalogue of splice junction sequences

21 January 2018

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

21 January 2018

1 reference

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

Multistep control of pituitary organogenesis.

21 January 2018

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

21 January 2018

1 reference

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

Early evolutionary origin of major homeodomain sequence classes

21 January 2018

1 reference

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