Detalhe da pesquisa
1.
ADH1B, the adipocyte-enriched alcohol dehydrogenase, plays an essential, cell-autonomous role in human adipogenesis.
Proc Natl Acad Sci U S A
; 121(24): e2319301121, 2024 Jun 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38838011
2.
Loss of thymidine phosphorylase activity disrupts adipocyte differentiation and induces insulin-resistant lipoatrophic diabetes.
BMC Med
; 20(1): 95, 2022 03 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-35341481
3.
Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real-life experience from a national reference network.
Diabetes Obes Metab
; 24(8): 1565-1577, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35445532
4.
Biallelic CAV1 null variants induce congenital generalized lipodystrophy with achalasia.
Eur J Endocrinol
; 185(6): 841-854, 2021 Nov 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-34643546
5.
Molecular and Cellular Bases of Lipodystrophy Syndromes.
Front Endocrinol (Lausanne)
; 12: 803189, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35046902
6.
EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence.
Elife
; 102021 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34342583