Detalhe da pesquisa
1.
Human oocytes reprogram adult somatic nuclei of a type 1 diabetic to diploid pluripotent stem cells.
Nature
; 510(7506): 533-6, 2014 Jun 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-24776804
2.
Loss of the imprinted, non-coding Snord116 gene cluster in the interval deleted in the Prader Willi syndrome results in murine neuronal and endocrine pancreatic developmental phenotypes.
Hum Mol Genet
; 26(23): 4606-4616, 2017 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28973544
3.
Prader-Willi-Like Phenotype Caused by an Atypical 15q11.2 Microdeletion.
Genes (Basel)
; 11(2)2020 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-31991769
4.
Hypomorphism of Fto and Rpgrip1l causes obesity in mice.
J Clin Invest
; 126(5): 1897-910, 2016 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27064284
5.
Gel formation in protein amyloid aggregation: a physical mechanism for cytotoxicity.
PLoS One
; 9(4): e94789, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24740416