Detalhe da pesquisa
1.
JAK inhibitor treatment for inborn errors of JAK/STAT signaling: An ESID/EBMT-IEWP retrospective study.
J Allergy Clin Immunol
; 153(1): 275-286.e18, 2024 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37935260
2.
Author Correction: Discovery of stimulation-responsive immune enhancers with CRISPR activation.
Nature
; 559(7715): E13, 2018 07.
Artigo
Inglês
| MEDLINE | ID: mdl-29899441
3.
Discovery of stimulation-responsive immune enhancers with CRISPR activation.
Nature
; 549(7670): 111-115, 2017 09 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28854172
4.
Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology.
J Allergy Clin Immunol
; 145(1): 46-69, 2020 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31568798
5.
B cell-intrinsic CD84 and Ly108 maintain germinal center B cell tolerance.
J Immunol
; 194(9): 4130-43, 2015 May 01.
Artigo
Inglês
| MEDLINE | ID: mdl-25801429
6.
Combined immunodeficiency due to MALT1 mutations, treated by hematopoietic cell transplantation.
J Clin Immunol
; 35(2): 135-46, 2015 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-25627829
7.
Autoantibody discovery across monogenic, acquired, and COVID-19-associated autoimmunity with scalable PhIP-seq.
Elife
; 112022 10 27.
Artigo
Inglês
| MEDLINE | ID: mdl-36300623
8.
Autoantibody discovery across monogenic, acquired, and COVID19-associated autoimmunity with scalable PhIP-Seq.
bioRxiv
; 2022 Mar 24.
Artigo
Inglês
| MEDLINE | ID: mdl-35350199
9.
CTLA-4 Haploinsufficiency Presenting as Extensive Enteropathy in a Patient With Very Early Onset Inflammatory Bowel Disease.
JPGN Rep
; 2(3): e099, 2021 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-37205940
10.
A human mutation in STAT3 promotes type 1 diabetes through a defect in CD8+ T cell tolerance.
J Exp Med
; 218(8)2021 08 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34115115
11.
Primary immune regulatory disorders: a growing universe of immune dysregulation.
Curr Opin Allergy Clin Immunol
; 20(6): 582-590, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-32941318
12.
Identification of novel, clinically correlated autoantigens in the monogenic autoimmune syndrome APS1 by proteome-wide PhIP-Seq.
Elife
; 92020 05 15.
Artigo
Inglês
| MEDLINE | ID: mdl-32410729
13.
Distinct interferon signatures and cytokine patterns define additional systemic autoinflammatory diseases.
J Clin Invest
; 130(4): 1669-1682, 2020 04 01.
Artigo
Inglês
| MEDLINE | ID: mdl-31874111
14.
Hematopoietic Cell Transplantation in Patients With Primary Immune Regulatory Disorders (PIRD): A Primary Immune Deficiency Treatment Consortium (PIDTC) Survey.
Front Immunol
; 11: 239, 2020.
Artigo
Inglês
| MEDLINE | ID: mdl-32153572
15.
The role of SAP and the SLAM family in autoimmunity.
Curr Opin Immunol
; 18(6): 656-64, 2006 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-17011767
16.
A large CRISPR-induced bystander mutation causes immune dysregulation.
Commun Biol
; 2: 70, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-30793048
17.
Analysis of pulmonary features and treatment approaches in the COPA syndrome.
ERJ Open Res
; 4(2)2018 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-29977900
18.
Unusual eye signs in Wegener's granulomatosis.
Hong Kong Med J
; 13(3): 241-2, 2007 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-17548916
19.
A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70.
J Exp Med
; 213(2): 155-65, 2016 Feb 08.
Artigo
Inglês
| MEDLINE | ID: mdl-26783323
20.
Electric shock wave lithotripsy (ESWL) as a pain control measure in dermatomyositis with calcinosis cutis-old method, new discovery.
Clin Rheumatol
; 24(2): 172-3, 2005 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-15565396