(Q34124860)

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AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.

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Europe PubMed Central

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31 July 2017

AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34. (English)

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31 July 2017

congenital disorder

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congenital generalized lipodystrophy

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Anne M. Bowcock

6

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Europe PubMed Central

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31 July 2017

Elif Arioglu Oral

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Elif Arioglu

2

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Anil K Agarwal

1

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31 July 2017

Salome De Almeida

3

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31 July 2017

Nurullah Akkoc

4

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31 July 2017

Simeon I Taylor

5

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31 July 2017

Robert I Barnes

7

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31 July 2017

Abhimanyu Garg

8

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31 July 2017

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publication date

22 April 2002

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31 July 2017

Nature Genetics

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31 July 2017

31

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31 July 2017

1

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31 July 2017

21-23

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31 July 2017

Human lysophosphatidic acid acyltransferase. cDNA cloning, expression, and localization to chromosome 9q34.3.

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https://api.crossref.org/works/10.1038%2FNG880

7 January 2021

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Cloning and Expression of Two Human Lysophosphatidic Acid Acyltransferase cDNAs That Enhance Cytokine-Induced Signaling Responses in Cells

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https://api.crossref.org/works/10.1038%2FNG880

7 January 2021

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Analysis of amino acid motifs diagnostic for the sn-glycerol-3-phosphate acyltransferase reaction

1 reference

https://api.crossref.org/works/10.1038%2FNG880

7 January 2021

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Lysophosphatidic acid synthesis and release

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https://api.crossref.org/works/10.1038%2FNG880

7 January 2021

based on heuristic

inferred from DOI database lookup

Lysophospholipids--receptor revelations

1 reference

https://api.crossref.org/works/10.1038%2FNG880

7 January 2021

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Phosphatidic acid-mediated mitogenic activation of mTOR signaling

1 reference

https://api.crossref.org/works/10.1038%2FNG880

7 January 2021

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Congenital lipodystrophy: An endocrine study in three siblings. I. Disorders of carbohydrate metabolism

1 reference

https://api.crossref.org/works/10.1038%2FNG880

7 January 2021

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Leptin-replacement therapy for lipodystrophy.

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https://api.crossref.org/works/10.1038%2FNG880

7 January 2021

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Europe PubMed Central

PubMed publication ID

31 July 2017

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Europe PubMed Central

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31 July 2017

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