Detalhe da pesquisa
1.
Somatic mutations in cerebral cortical malformations.
N Engl J Med
; 371(8): 733-43, 2014 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-25140959
2.
Machine-learning classification identifies patients with early systemic sclerosis as abatacept responders via CD28 pathway modulation.
JCI Insight
; 7(24)2022 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36355434
3.
Mast Cell Activation in the Systemic Sclerosis Esophagus.
J Scleroderma Relat Disord
; 6(1): 77-86, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34179507
4.
Molecular "omic" signatures in systemic sclerosis.
Eur J Rheumatol
; 7(Suppl 3): S173-S180, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-33164732
5.
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorder.
Sci Rep
; 10(1): 14045, 2020 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-32820185
6.
Microbiome dysbiosis is associated with disease duration and increased inflammatory gene expression in systemic sclerosis skin.
Arthritis Res Ther
; 21(1): 49, 2019 02 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30728065
7.
Cell lineage analysis in human brain using endogenous retroelements.
Neuron
; 85(1): 49-59, 2015 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25569347
8.
Somatic mutation in single human neurons tracks developmental and transcriptional history.
Science
; 350(6256): 94-98, 2015 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26430121
9.
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain.
Cell Rep
; 8(5): 1280-9, 2014 Sep 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-25159146
10.
Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain.
Cell Rep
; 10(4): 645, 2015 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25832109