Detalhe da pesquisa
1.
Early Fate Defines Microglia and Non-parenchymal Brain Macrophage Development.
Cell
; 181(3): 557-573.e18, 2020 04 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32259484
2.
Histone Acetylome-wide Association Study of Autism Spectrum Disorder.
Cell
; 167(5): 1385-1397.e11, 2016 11 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-27863250
3.
A single-cell atlas identifies pretreatment features of primary imatinib resistance in chronic myeloid leukemia.
Blood
; 141(22): 2738-2755, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36857629
4.
Shared and unique transcriptomic signatures of antidepressant and probiotics action in the mammalian brain.
Mol Psychiatry
; 2024 Jun 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38844534
5.
Comprehensive molecular phenotyping of ARID1A-deficient gastric cancer reveals pervasive epigenomic reprogramming and therapeutic opportunities.
Gut
; 72(9): 1651-1663, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36918265
6.
Integrative multi-omics landscape of fluoxetine action across 27 brain regions reveals global increase in energy metabolism and region-specific chromatin remodelling.
Mol Psychiatry
; 27(11): 4510-4525, 2022 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-36056172
7.
RCA2: a scalable supervised clustering algorithm that reduces batch effects in scRNA-seq data.
Nucleic Acids Res
; 49(15): 8505-8519, 2021 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34320202
8.
Epigenomes of Human Hearts Reveal New Genetic Variants Relevant for Cardiac Disease and Phenotype.
Circ Res
; 127(6): 761-777, 2020 08 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-32529949
9.
Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease.
Proc Natl Acad Sci U S A
; 116(19): 9622-9627, 2019 05 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31015293
10.
scConsensus: combining supervised and unsupervised clustering for cell type identification in single-cell RNA sequencing data.
BMC Bioinformatics
; 22(1): 186, 2021 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33845760
11.
Transposable elements that have recently been mobile in the human genome.
BMC Genomics
; 22(1): 789, 2021 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34732136
12.
Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue.
Hum Mol Genet
; 28(13): 2201-2211, 2019 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31220268
13.
Robust CTCF-Based Chromatin Architecture Underpins Epigenetic Changes in the Heart Failure Stress-Gene Response.
Circulation
; 139(16): 1937-1956, 2019 04 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-30717603
14.
DNA-mediated dimerization on a compact sequence signature controls enhancer engagement and regulation by FOXA1.
Nucleic Acids Res
; 46(11): 5470-5486, 2018 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29669022
15.
Ncoa3 functions as an essential Esrrb coactivator to sustain embryonic stem cell self-renewal and reprogramming.
Genes Dev
; 26(20): 2286-98, 2012 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23019124
16.
Comprehensive benchmarking reveals H2BK20 acetylation as a distinctive signature of cell-state-specific enhancers and promoters.
Genome Res
; 26(5): 612-23, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26957309
17.
The transcription factor SOX6 contributes to the developmental origins of obesity by promoting adipogenesis.
Development
; 143(6): 950-61, 2016 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26893351
18.
Concurrent Single-Cell RNA and Targeted DNA Sequencing on an Automated Platform for Comeasurement of Genomic and Transcriptomic Signatures.
Clin Chem
; 65(2): 272-281, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30523199
19.
Massive contribution of transposable elements to mammalian regulatory sequences.
Semin Cell Dev Biol
; 57: 51-56, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27174439
20.
MiR-135b is a direct PAX6 target and specifies human neuroectoderm by inhibiting TGF-ß/BMP signaling.
EMBO J
; 33(11): 1271-83, 2014 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-24802670