Detalhe da pesquisa
1.
Transcription factor-mediated intestinal metaplasia and the role of a shadow enhancer.
Genes Dev
; 36(1-2): 38-52, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34969824
2.
Dissecting dual roles of MyoD during lineage conversion to mature myocytes and myogenic stem cells.
Genes Dev
; 35(17-18): 1209-1228, 2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34413137
3.
Prolonged Mek1/2 suppression impairs the developmental potential of embryonic stem cells.
Nature
; 548(7666): 219-223, 2017 08 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28746311
4.
Reduced MEK inhibition preserves genomic stability in naive human embryonic stem cells.
Nat Methods
; 15(9): 732-740, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30127506
5.
Dissection of gastric homeostasis in vivo facilitates permanent capture of isthmus-like stem cells in vitro.
Nat Cell Biol
; 25(3): 390-403, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36717627
6.
H3K36 methylation maintains cell identity by regulating opposing lineage programmes.
Nat Cell Biol
; 25(8): 1121-1134, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37460697
7.
Inducible histone K-to-M mutations are dynamic tools to probe the physiological role of site-specific histone methylation in vitro and in vivo.
Nat Cell Biol
; 21(11): 1449-1461, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31659274
8.
The RNA Helicase DDX6 Controls Cellular Plasticity by Modulating P-Body Homeostasis.
Cell Stem Cell
; 25(5): 622-638.e13, 2019 11 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31588046
9.
An Intermediate Pluripotent State Controlled by MicroRNAs Is Required for the Naive-to-Primed Stem Cell Transition.
Cell Stem Cell
; 22(6): 851-864.e5, 2018 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29804889
10.
Direct Reprogramming of Mouse Fibroblasts into Functional Skeletal Muscle Progenitors.
Stem Cell Reports
; 10(5): 1505-1521, 2018 05 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29742392
11.
DUSP9 Modulates DNA Hypomethylation in Female Mouse Pluripotent Stem Cells.
Cell Stem Cell
; 20(5): 706-719.e7, 2017 05 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28366588
12.
Lce1 Family Members Are Nrf2-Target Genes that Are Induced to Compensate for the Loss of Loricrin.
J Invest Dermatol
; 136(8): 1656-1663, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27167730
13.
Sox2 Suppresses Gastric Tumorigenesis in Mice.
Cell Rep
; 16(7): 1929-41, 2016 08 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-27498859
14.
Lineage conversion induced by pluripotency factors involves transient passage through an iPSC stage.
Nat Biotechnol
; 33(7): 761-8, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-26098450
15.
Activation of Nrf2 in keratinocytes causes chloracne (MADISH)-like skin disease in mice.
EMBO Mol Med
; 6(4): 442-57, 2014 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-24503019
16.
Aurora kinase-A deficiency during skin development impairs cell division and stratification.
J Invest Dermatol
; 133(1): 78-86, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22832491
17.
Amniotic fluid activates the nrf2/keap1 pathway to repair an epidermal barrier defect in utero.
Dev Cell
; 23(6): 1238-46, 2012 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23237955
18.
Nrf2 links epidermal barrier function with antioxidant defense.
EMBO Mol Med
; 4(5): 364-79, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22383093