Detalhe da pesquisa
1.
High-Dimensional Analysis Delineates Myeloid and Lymphoid Compartment Remodeling during Successful Immune-Checkpoint Cancer Therapy.
Cell
; 175(4): 1014-1030.e19, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30343900
2.
CpG Island Hypermethylation Mediated by DNMT3A Is a Consequence of AML Progression.
Cell
; 168(5): 801-816.e13, 2017 02 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-28215704
3.
Subsets of ILC3-ILC1-like cells generate a diversity spectrum of innate lymphoid cells in human mucosal tissues.
Nat Immunol
; 20(8): 980-991, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31209406
4.
Publisher Correction: Subsets of ILC3-ILC1-like cells generate a diversity spectrum of innate lymphoid cells in human mucosal tissues.
Nat Immunol
; 20(10): 1405, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-31388149
5.
Sequencing the mouse Y chromosome reveals convergent gene acquisition and amplification on both sex chromosomes.
Cell
; 159(4): 800-13, 2014 Nov 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-25417157
6.
A draft human pangenome reference.
Nature
; 617(7960): 312-324, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37165242
7.
High-Dimensional Analysis Delineates Myeloid and Lymphoid Compartment Remodeling during Successful Immune-Checkpoint Cancer Therapy.
Cell
; 175(5): 1443, 2018 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30445041
8.
The Human Pangenome Project: a global resource to map genomic diversity.
Nature
; 604(7906): 437-446, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35444317
9.
Semi-automated assembly of high-quality diploid human reference genomes.
Nature
; 611(7936): 519-531, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36261518
10.
Genomic landscape of non-small cell lung cancer in smokers and never-smokers.
Cell
; 150(6): 1121-34, 2012 Sep 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-22980976
11.
The origin and evolution of mutations in acute myeloid leukemia.
Cell
; 150(2): 264-78, 2012 Jul 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-22817890
12.
Telomere-to-telomere assembly of a complete human X chromosome.
Nature
; 585(7823): 79-84, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32663838
13.
A human genome structural variation sequencing resource reveals insights into mutational mechanisms.
Cell
; 143(5): 837-47, 2010 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21111241
14.
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
; 575(7783): E4, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31686056
15.
Exome sequencing of Finnish isolates enhances rare-variant association power.
Nature
; 572(7769): 323-328, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31367044
16.
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.
N Engl J Med
; 384(10): 924-935, 2021 03 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33704937
17.
IL-1ß expression in bone marrow dendritic cells is induced by TLR2 agonists and regulates HSC function.
Blood
; 140(14): 1607-1620, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35675516
18.
Immunosuppression and outcomes in adult patients with de novo acute myeloid leukemia with normal karyotypes.
Proc Natl Acad Sci U S A
; 118(49)2021 12 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34845035
19.
Author Correction: Comparative and demographic analysis of orang-utan genomes.
Nature
; 608(7924): E36, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35962045
20.
Remethylation of Dnmt3a-/- hematopoietic cells is associated with partial correction of gene dysregulation and reduced myeloid skewing.
Proc Natl Acad Sci U S A
; 117(6): 3123-3134, 2020 02 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31996479