Serum amino acids in patients with mutations in the hepatocyte nuclear factor-1 alpha gene. (Q44990848)

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31 December 2019

title

Serum amino acids in patients with mutations in the hepatocyte nuclear factor-1 alpha gene (English)

1 reference

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2

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author name string

Stride A

1

1 reference

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31 December 2019

Brown A

3

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31 December 2019

Gooding K

4

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31 December 2019

Castleden HA

5

1 reference

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Hattersley AT

6

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publication date

1 August 2004

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31 December 2019

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volume

21

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issue

8

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page(s)

928-930

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MODY in Iceland is associated with mutations in HNF-1alpha and a novel mutation in NeuroD1.

31 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-5491.2004.01107.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-5491.2004.01107.X

Hepatocyte nuclear factor-1alpha is an essential regulator of bile acid and plasma cholesterol metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-5491.2004.01107.X

Identification of hepatic nuclear factor 1 binding sites in the 5' flanking region of the human phenylalanine hydroxylase gene: implication of a dual function of phenylalanine hydroxylase stimulator in the phenylalanine hydroxylation system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-5491.2004.01107.X

The activity of the highly inducible mouse phenylalanine hydroxylase gene promoter is dependent upon a tissue-specific, hormone-inducible enhancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-5491.2004.01107.X

Conserved as well as divergent regulatory elements account for expression of the human and rodent phenylalanine hydroxylase genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-5491.2004.01107.X

10.1111/J.1464-5491.2004.01107.X

21 January 2018

Identifiers

DOI

1 reference

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31 December 2019

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