(Q43941053)

28 November 2017

title

A novel mutation in PIT-1: phenotypic variability in familial combined pituitary hormone deficiencies (English)

1 reference

28 November 2017

Gat-Yablonski G

1

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28 November 2017

Lazar L

series ordinal

2

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28 November 2017

Pertzelan A

series ordinal

3

1 reference

28 November 2017

Phillip M

series ordinal

4

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28 November 2017

publication date

1 March 2002

1 reference

Journal of Pediatric Endocrinology and Metabolism

28 November 2017

published in

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28 November 2017

volume

15

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28 November 2017

issue

3

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28 November 2017

page(s)

325-330

1 reference

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

28 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

A tissue-specific transcription factor containing a homeodomain specifies a pituitary phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

Transcription factors regulating pituitary development

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

In Vivo Mutational Analysis of the DNA Binding Domain of the Tissue-specific Transcription Factor, Pit-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

Allosteric effects of Pit-1 DNA sites on long-term repression in cell type specification

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2002.15.3.325

10.1515/JPEM.2002.15.3.325

21 January 2018

Identifiers

DOI

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28 November 2017

1 reference