Detalhe da pesquisa
1.
TOP1 inhibition therapy protects against SARS-CoV-2-induced lethal inflammation.
Cell
; 184(10): 2618-2632.e17, 2021 05 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33836156
2.
The RNA Exosome Syncs IAV-RNAPII Transcription to Promote Viral Ribogenesis and Infectivity.
Cell
; 169(4): 679-692.e14, 2017 05 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28475896
3.
Nuclear RNA catabolism controls endogenous retroviruses, gene expression asymmetry, and dedifferentiation.
Mol Cell
; 83(23): 4255-4271.e9, 2023 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37995687
4.
Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4.
Nature
; 606(7916): 945-952, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35732742
5.
Author Correction: Clonally expanded CD8 T cells characterize amyotrophic lateral sclerosis-4.
Nature
; 608(7924): E34, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35945277
6.
Convergence of cytokine dysregulation and antibody deficiency in common variable immunodeficiency with inflammatory complications.
J Allergy Clin Immunol
; 149(1): 315-326.e9, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34146579
7.
Whole-Genome Sequencing Identifies STAT4 as a Putative Susceptibility Gene in Classic Kaposi Sarcoma.
J Infect Dis
; 211(11): 1842-51, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25492914
8.
Whole-exome-sequencing-based discovery of human FADD deficiency.
Am J Hum Genet
; 87(6): 873-81, 2010 Dec 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21109225
9.
Disseminated Cutaneous Warts in X-Linked Hyper IgM Syndrome.
J Clin Immunol
; 38(4): 454-456, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29730845
10.
DNMT3A haploinsufficiency causes dichotomous DNA methylation defects at enhancers in mature human immune cells.
J Exp Med
; 218(7)2021 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33970190
11.
Topoisomerase 1 inhibition therapy protects against SARS-CoV-2-induced inflammation and death in animal models.
bioRxiv
; 2020 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33299999
12.
Influenza virus infection causes global RNAPII termination defects.
Nat Struct Mol Biol
; 25(9): 885-893, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30177761
13.
Autosomal Recessive Cardiomyopathy Presenting as Acute Myocarditis.
J Am Coll Cardiol
; 69(13): 1653-1665, 2017 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28359509
14.
TLR3 deficiency in herpes simplex encephalitis: high allelic heterogeneity and recurrence risk.
Neurology
; 83(21): 1888-97, 2014 Nov 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25339207
15.
A novel FAS mutation with variable expressivity in a family with unicentric and idiopathic multicentric Castleman disease.
Blood Adv
; 2(21): 2959-2963, 2018 11 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30404775
16.
Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia.
Science
; 340(6135): 976-8, 2013 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-23579497
17.
Inherited human OX40 deficiency underlying classic Kaposi sarcoma of childhood.
J Exp Med
; 210(9): 1743-59, 2013 Aug 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-23897980
18.
A major locus on chromosome 3p22 conferring predisposition to human herpesvirus 8 infection.
Eur J Hum Genet
; 20(6): 690-5, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22258534
19.
A mild form of SLC29A3 disorder: a frameshift deletion leads to the paradoxical translation of an otherwise noncoding mRNA splice variant.
PLoS One
; 7(1): e29708, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22238637
20.
Multicentric Castleman disease in an HHV8-infected child born to consanguineous parents with systematic review.
Pediatrics
; 129(1): e199-203, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22157133