Detalhe da pesquisa
1.
CRISPR-Based Tools in Immunity.
Annu Rev Immunol
; 37: 571-597, 2019 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-30698999
2.
Functional CRISPR dissection of gene networks controlling human regulatory T cell identity.
Nat Immunol
; 21(11): 1456-1466, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32989329
3.
Thymic regulatory T cells arise via two distinct developmental programs.
Nat Immunol
; 20(2): 195-205, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30643267
4.
CRISPR screen in regulatory T cells reveals modulators of Foxp3.
Nature
; 582(7812): 416-420, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32499641
5.
Author Correction: Discovery of stimulation-responsive immune enhancers with CRISPR activation.
Nature
; 559(7715): E13, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29899441
6.
Discovery of stimulation-responsive immune enhancers with CRISPR activation.
Nature
; 549(7670): 111-115, 2017 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28854172
7.
Dysregulated RASGRP1 expression through RUNX1 mediated transcription promotes autoimmunity.
Eur J Immunol
; 51(2): 471-482, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33065764
8.
Generation of knock-in primary human T cells using Cas9 ribonucleoproteins.
Proc Natl Acad Sci U S A
; 112(33): 10437-42, 2015 Aug 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-26216948
9.
"T-bet"-ing on autoimmunity variants.
PLoS Genet
; 13(9): e1006924, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28880873
10.
A divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3).
Biochim Biophys Acta
; 1833(3): 468-78, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-23103514
11.
ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination.
Am J Med Genet A
; 164A(11): 2892-900, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25251875
12.
DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics.
Hum Mutat
; 34(6): 827-35, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23504663
13.
Non-coding sequence variation reveals fragility within interleukin 2 feedback circuitry and shapes autoimmune disease risk.
bioRxiv
; 2023 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-37503101
14.
The lncRNA Malat1 Inhibits miR-15/16 to Enhance Cytotoxic T Cell Activation and Memory Cell Formation.
bioRxiv
; 2023 Jul 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-37547023
15.
VAR-MD: a tool to analyze whole exome-genome variants in small human pedigrees with mendelian inheritance.
Hum Mutat
; 33(4): 593-8, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22290570
16.
The mechanical properties of Drosophila jump muscle expressing wild-type and embryonic Myosin isoforms.
Biophys J
; 98(7): 1218-26, 2010 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20371321
17.
A large CRISPR-induced bystander mutation causes immune dysregulation.
Commun Biol
; 2: 70, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30793048
18.
Enhancer connectome in primary human cells identifies target genes of disease-associated DNA elements.
Nat Genet
; 49(11): 1602-1612, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28945252
19.
GRIN2A mutation and early-onset epileptic encephalopathy: personalized therapy with memantine.
Ann Clin Transl Neurol
; 1(3): 190-198, 2014 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24839611
20.
Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration.
Eur J Hum Genet
; 20(4): 476-9, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22146942