Detalhe da pesquisa
1.
Epigenomic analysis of multilineage differentiation of human embryonic stem cells.
Cell
; 153(5): 1134-48, 2013 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-23664764
2.
Systematic identification of genotype-dependent enhancer variants in eosinophilic esophagitis.
Am J Hum Genet
; 111(2): 280-294, 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38183988
3.
Epigenetic and transcriptional dysregulation in CD4+ T cells in patients with atopic dermatitis.
PLoS Genet
; 18(5): e1009973, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35576187
4.
Shared and distinct interactions of type 1 and type 2 Epstein-Barr Nuclear Antigen 2 with the human genome.
BMC Genomics
; 25(1): 273, 2024 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38475709
5.
Epstein-Barr virus nuclear antigen 2 extensively rewires the human chromatin landscape at autoimmune risk loci.
Genome Res
; 31(12): 2185-2198, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34799401
6.
Epigenetic Analysis of the Chromatin Landscape Identifies a Repertoire of Murine Eosinophil-Specific PU.1-Bound Enhancers.
J Immunol
; 207(4): 1044-1054, 2021 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34330753
7.
5mC oxidation by Tet2 modulates enhancer activity and timing of transcriptome reprogramming during differentiation.
Mol Cell
; 56(2): 286-297, 2014 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-25263596
8.
Integrative analysis of haplotype-resolved epigenomes across human tissues.
Nature
; 518(7539): 350-354, 2015 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25693566
9.
A comparative encyclopedia of DNA elements in the mouse genome.
Nature
; 515(7527): 355-64, 2014 Nov 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25409824
10.
Incomplete MyoD-induced transdifferentiation is associated with chromatin remodeling deficiencies.
Nucleic Acids Res
; 45(20): 11684-11699, 2017 Nov 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-28977539
11.
A map of the cis-regulatory sequences in the mouse genome.
Nature
; 488(7409): 116-20, 2012 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-22763441
12.
DNA binding by FOXP3 domain-swapped dimer suggests mechanisms of long-range chromosomal interactions.
Nucleic Acids Res
; 43(2): 1268-82, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25567984
13.
Global DNA hypomethylation coupled to repressive chromatin domain formation and gene silencing in breast cancer.
Genome Res
; 22(2): 246-58, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22156296
14.
Human DNA methylomes at base resolution show widespread epigenomic differences.
Nature
; 462(7271): 315-22, 2009 Nov 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-19829295
15.
Human cytomegalovirus infection coopts chromatin organization to diminish TEAD1 transcription factor activity.
bioRxiv
; 2024 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38645179
16.
Distinct patterns of somatic alterations in a lymphoblastoid and a tumor genome derived from the same individual.
Nucleic Acids Res
; 39(14): 6056-68, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21493686
17.
The medicinal leech genome encodes 21 innexin genes: different combinations are expressed by identified central neurons.
Dev Genes Evol
; 222(1): 29-44, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22358128
18.
Construction of a medicinal leech transcriptome database and its application to the identification of leech homologs of neural and innate immune genes.
BMC Genomics
; 11: 407, 2010 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-20579359
19.
Evaluating Chromatin Accessibility Differences Across Multiple Primate Species Using a Joint Modeling Approach.
Genome Biol Evol
; 11(10): 3035-3053, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31599933
20.
Exome analysis identified a novel mutation in the RBP4 gene in a consanguineous pedigree with retinal dystrophy and developmental abnormalities.
PLoS One
; 7(11): e50205, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-23189188