Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2). (Q33867754)

29 July 2017

title

Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2). (English)

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29 July 2017

1

P E Macchia

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29 July 2017

M G Mattei

2

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29 July 2017

P Lapi

series ordinal

3

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29 July 2017

G Fenzi

series ordinal

4

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29 July 2017

R Di Lauro

series ordinal

5

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29 July 2017

publication date

1 May 1999

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29 July 2017

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29 July 2017

volume

81

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29 July 2017

issue

5

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29 July 2017

page(s)

433-440

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Polymorphic DNA region adjacent to the 5' end of the human insulin gene

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

1 reference

7 January 2021

DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Transcriptional regulation in mammalian cells by sequence-specific DNA binding proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Drosophila Krüppel protein is a transcriptional repressor.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Pituitary cell phenotypes involve cell-specific Pit-1 mRNA translation and synergistic interactions with other classes of transcription factors

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Transcriptional regulation of liver-specific gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Cell-type-specific expression of the rat thyroperoxidase promoter indicates common mechanisms for thyroid-specific gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Congenital hypothyroidism

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Co-crystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Neonatal screening for congenital hypothyroidism.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Guidelines for neonatal screening programmes for congenital hypothyroidism. Working group on congenital hypothyroidism of the European Society for Paediatric Endocrinology.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Six members of the mouse forkhead gene family are developmentally regulated

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

New eukaryotic transcriptional repressors.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Thyroid-specific gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

The HNF-3 gene family of transcription factors in mice: gene structure, cDNA sequence, and mRNA distribution

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Genomic structure of HOXD13 gene: a nine polyalanine duplication causes synpolydactyly in two unrelated families

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Active repression mechanisms of eukaryotic transcription repressors

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

The T/ebp null mouse: thyroid-specific enhancer-binding protein is essential for the organogenesis of the thyroid, lung, ventral forebrain, and pituitary

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Hepatocyte nuclear factor 1 inactivation results in hepatic dysfunction, phenylketonuria, and renal Fanconi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Redox properties of cytochrome c nitrite reductase from Desulfovibrio desulfuricans ATCC 27774

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

FKHL15, a new human member of the forkhead gene family located on chromosome 9q22

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

A mouse model for hereditary thyroid dysgenesis and cleft palate

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

Follicular cells of the thyroid gland require Pax8 gene function

1 reference

https://api.crossref.org/works/10.1016%2FS0300-9084%2899%2980092-3

7 January 2021

10.1016/S0300-9084(99)80092-3

Identifiers

DOI

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29 July 2017

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