Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice (Q24551193)

GOA release 2020-03-11

author name string

Joachim Pohlenz

1

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Alexandra Dumitrescu

2

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Dorothee Zundel

3

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Ursula Martiné

4

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Winfried Schönberger

5

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Eugene Koo

6

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Roy E Weiss

7

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Ronald N Cohen

8

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Shioko Kimura

9

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Samuel Refetoff

Journal of Clinical Investigation

10

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language of work or name

English

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publication date

February 2002

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published in

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volume

109

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issue

4

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page(s)

469-73

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cites work

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

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Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failure

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Human, bovine, canine and rat thyroglobulin promoter sequences display species-specific differences in an in vitro study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11854318