Detalhe da pesquisa
1.
Clinical and molecular correlates of somatic and germline DDX41 variants in patients and families with myeloid neoplasms.
Haematologica
; 108(11): 3033-3043, 2023 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37199125
2.
Chronic immune response dysregulation in MDS pathogenesis.
Blood
; 132(15): 1553-1560, 2018 10 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30104218
3.
Cofactor-mediated restriction of GATA-1 chromatin occupancy coordinates lineage-specific gene expression.
Mol Cell
; 47(4): 608-21, 2012 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-22771118
4.
Germline DDX41 mutant predisposition syndromes: Slow driver states to hematological malignancies.
Am J Hematol
; 98(11): 1673-1676, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37705260
5.
Combinatorial regulation of tissue specification by GATA and FOG factors.
Development
; 139(21): 3905-16, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23048181
6.
High-risk human papillomavirus E6 protein promotes reprogramming of Fanconi anemia patient cells through repression of p53 but does not allow for sustained growth of induced pluripotent stem cells.
J Virol
; 88(19): 11315-26, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25031356
7.
Perturbation of fetal hematopoiesis in a mouse model of Down syndrome's transient myeloproliferative disorder.
Blood
; 122(6): 988-98, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23719302
8.
Ikaros inhibits megakaryopoiesis through functional interaction with GATA-1 and NOTCH signaling.
Blood
; 121(13): 2440-51, 2013 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-23335373
9.
Global transcriptome and chromatin occupancy analysis reveal the short isoform of GATA1 is deficient for erythroid specification and gene expression.
Haematologica
; 100(5): 575-84, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25682601
10.
Chromatin occupancy analysis reveals genome-wide GATA factor switching during hematopoiesis.
Blood
; 119(16): 3724-33, 2012 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-22383799
11.
Germline and Somatic Defects in DDX41 and its Impact on Myeloid Neoplasms.
Curr Hematol Malig Rep
; 17(5): 113-120, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35781188
12.
The deubiquitinase USP15 modulates cellular redox and is a therapeutic target in acute myeloid leukemia.
Leukemia
; 36(2): 438-451, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34465865
13.
Germline DDX41 mutations cause ineffective hematopoiesis and myelodysplasia.
Cell Stem Cell
; 28(11): 1966-1981.e6, 2021 11 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34473945
14.
Inherited DNA Repair Defects Disrupt the Structure and Function of Human Skin.
Cell Stem Cell
; 28(3): 424-435.e6, 2021 03 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33232662
15.
HeyL regulates the number of TrkC neurons in dorsal root ganglia.
Dev Biol
; 334(1): 142-51, 2009 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-19631204
16.
Retinoids modulate expression of the endocytic partners megalin, cubilin, and disabled-2 and uptake of vitamin D-binding protein in human mammary cells.
J Nutr
; 138(7): 1323-8, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18567755
17.
Reduction in PU.1 activity results in a block to B-cell development, abnormal myeloid proliferation, and neonatal lethality.
Exp Hematol
; 35(7): 1056-68, 2007 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-17588474
18.
Microarray reveals complement components are regulated in the serum-deprived rat retinal ganglion cell line.
Mol Vis
; 13: 293-308, 2007 Feb 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-17356516
19.
Overcoming Pluripotent Stem Cell Dependence on the Repair of Endogenous DNA Damage.
Stem Cell Reports
; 6(1): 44-54, 2016 Jan 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26771352
20.
Increased dosage of the chromosome 21 ortholog Dyrk1a promotes megakaryoblastic leukemia in a murine model of Down syndrome.
J Clin Invest
; 122(3): 948-62, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22354171