Detalhe da pesquisa
1.
A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect.
Am J Hum Genet
; 98(5): 981-992, 2016 05 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27108798
2.
Acute multiple organ failure in adult mice deleted for the developmental regulator Wt1.
PLoS Genet
; 7(12): e1002404, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22216009
3.
Toll-like receptor 2 orchestrates a tumor suppressor response in non-small cell lung cancer.
Cell Rep
; 41(6): 111596, 2022 11 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36351380
4.
Embryonic mesothelial-derived hepatic lineage of quiescent and heterogenous scar-orchestrating cells defined but suppressed by WT1.
Nat Commun
; 10(1): 4688, 2019 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31615982
5.
Loss of ALDH18A1 function is associated with a cellular lipid droplet phenotype suggesting a link between autosomal recessive cutis laxa type 3A and Warburg Micro syndrome.
Mol Genet Genomic Med
; 2(4): 319-25, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25077174