6 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 32117065 | Congenital Generalized Lipoatrophy (Berardinelli-Seip Syndrome) Type 1: Description of Novel AGPAT2 Homozygous Variants Showing the Highly Heterogeneous Presentation of the Disease. | 2020 | 4 |
2 | 29908837 | Expression of AGPAT2, an enzyme involved in the glycerophospholipid/triacylglycerol biosynthesis pathway, is directly regulated by HIF-1 and promotes survival and etoposide resistance of cancer cells under hypoxia. | 2018 Sep | 1 |
3 | 30319454 | A Single Complex Agpat2 Allele in a Patient With Partial Lipodystrophy. | 2018 | 1 |
4 | 16000584 | Induction of apoptosis using inhibitors of lysophosphatidic acid acyltransferase-beta and anti-CD20 monoclonal antibodies for treatment of human non-Hodgkin's lymphomas. | 2005 Jul 1 | 2 |
5 | 14557833 | Genetic basis of congenital generalized lipodystrophy. | 2004 Feb | 1 |
6 | 11967537 | AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34. | 2002 May | 1 |