(Q24317343)

congenital hypothyroidism

GOA release 2020-03-11

1 reference

1 reference

1

P E Macchia

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Caterina Missero

object named as

C Missero

5

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Meinrad Busslinger

object named as

M Busslinger

13

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author name string

P Lapi

2

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H Krude

3

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M T Pirro

4

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L Chiovato

6

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A Souabni

7

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M Baserga

8

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V Tassi

9

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A Pinchera

10

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G Fenzi

11

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A Grüters

12

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R Di Lauro

https://scigraph.springernature.com/pub.10.1038/ng0598-83

14

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language of work or name

English

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publication date

May 1998

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published in

Nature Genetics

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volume

19

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page(s)

83-6

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issue

1

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exact match

0 references

cites work

Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9

1 reference

https://api.crossref.org/works/10.1038/NG0598-83

Crystal structure of a paired domain-DNA complex at 2.5 A resolution reveals structural basis for Pax developmental mutations

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0598-83

Follicular cells of the thyroid gland require Pax8 gene function

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0598-83

Follow-up at ages 5 and 7 years on mental development in children with hypothyroidism detected by Quebec Screening Program

20 April 2017

1 reference

Pax-8, a paired domain-containing protein, binds to a sequence overlapping the recognition site of a homeodomain and activates transcription from two thyroid-specific promoters

21 January 2018

1 reference

Alternative splicing of Pax-8 gene transcripts is developmentally regulated and generates isoforms with different transactivation properties

21 January 2018

1 reference

Disruption of base-paired U4.U6 small nuclear RNAs induced by mammalian heterogeneous nuclear ribonucleoprotein C protein

21 January 2018

1 reference

21 January 2018

1 reference

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

21 January 2018

1 reference

Long-term effects of L-thyroxine therapy for congenital hypothyroidism.

21 January 2018

1 reference

7 January 2021

Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland

1 reference

7 January 2021

PAX genes: what's new in developmental biology and cancer?

1 reference

7 January 2021

Distinct functional properties of three human paired-box-protein, PAX8, isoforms generated by alternative splicing in thyroid, kidney and Wilms' tumors

1 reference

7 January 2021

Pax-5 encodes the transcription factor BSAP and is expressed in B lymphocytes, the developing CNS, and adult testis

1 reference

7 January 2021

Function of the homeo and paired domain proteins TTF-1 and Pax-8 in thyroid cell proliferation

1 reference

7 January 2021

Preliminary report on a mass screening program for neonatal hypothyroidism

1 reference

7 January 2021

DNA sequence recognition by Pax proteins: bipartite structure of the paired domain and its binding site.

1 reference

7 January 2021