Detalhe da pesquisa
1.
DNA polymerase-α regulates the activation of type I interferons through cytosolic RNA:DNA synthesis.
Nat Immunol
; 17(5): 495-504, 2016 May.
Artigo
Inglês
| MEDLINE | ID: mdl-27019227
2.
Genotype, oxidase status, and preceding infection or autoinflammation do not affect allogeneic HCT outcomes for CGD.
Blood
; 142(24): 2105-2118, 2023 12 14.
Artigo
Inglês
| MEDLINE | ID: mdl-37562003
3.
Allogeneic hematopoietic cell transplantation is effective for p47phox chronic granulomatous disease: A Primary Immune Deficiency Treatment Consortium study.
J Allergy Clin Immunol
; 153(5): 1423-1431.e2, 2024 May.
Artigo
Inglês
| MEDLINE | ID: mdl-38290608
4.
Epigenetic and immunological indicators of IPEX disease in subjects with FOXP3 gene mutation.
J Allergy Clin Immunol
; 151(1): 233-246.e10, 2023 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36152823
5.
Intestinal microbiome and metabolome signatures in patients with chronic granulomatous disease.
J Allergy Clin Immunol
; 152(6): 1619-1633.e11, 2023 12.
Artigo
Inglês
| MEDLINE | ID: mdl-37659505
6.
SARS-CoV-2-Reactive Mucosal B Cells in the Upper Respiratory Tract of Uninfected Individuals.
J Immunol
; 207(10): 2581-2588, 2021 11 15.
Artigo
Inglês
| MEDLINE | ID: mdl-34607939
7.
Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients.
J Clin Immunol
; 42(8): 1748-1765, 2022 11.
Artigo
Inglês
| MEDLINE | ID: mdl-35947323
8.
Platelet-activating factor acetylhydrolase is a biomarker of severe anaphylaxis in children.
Allergy
; 77(9): 2665-2676, 2022 09.
Artigo
Inglês
| MEDLINE | ID: mdl-35396721
9.
FCRL4 Is an Fc Receptor for Systemic IgA, but Not Mucosal Secretory IgA.
J Immunol
; 205(2): 533-538, 2020 07 15.
Artigo
Inglês
| MEDLINE | ID: mdl-32513851
10.
Morbidity in an adenosine deaminase-deficient patient during 27 years of enzyme replacement therapy.
Clin Immunol
; 211: 108321, 2020 02.
Artigo
Inglês
| MEDLINE | ID: mdl-31812707
11.
Correction to: A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency.
J Clin Immunol
; 40(8): 1102, 2020 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-32901356
12.
A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency.
J Clin Immunol
; 40(8): 1093-1101, 2020 11.
Artigo
Inglês
| MEDLINE | ID: mdl-32813180
13.
Antibodies Encoded by FCRL4-Bearing Memory B Cells Preferentially Recognize Commensal Microbial Antigens.
J Immunol
; 200(12): 3962-3969, 2018 06 15.
Artigo
Inglês
| MEDLINE | ID: mdl-29703863
14.
Conversion from tacrolimus to sirolimus as a treatment modality in de novo allergies and immune-mediated disorders in pediatric liver transplant recipients.
Pediatr Transplant
; 24(6): e13737, 2020 09.
Artigo
Inglês
| MEDLINE | ID: mdl-32428390
15.
Consensus approach for the management of severe combined immune deficiency caused by adenosine deaminase deficiency.
J Allergy Clin Immunol
; 143(3): 852-863, 2019 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30194989
16.
Outcome of hematopoietic cell transplantation for DNA double-strand break repair disorders.
J Allergy Clin Immunol
; 141(1): 322-328.e10, 2018 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28392333
17.
Hematological Malignancies Associated With Primary Immunodeficiency Disorders.
Clin Immunol
; 194: 46-59, 2018 09.
Artigo
Inglês
| MEDLINE | ID: mdl-29966714
18.
De Novo Allergy and Immune-Mediated Disorders Following Solid-Organ Transplantation-Prevalence, Natural History, and Risk Factors.
J Pediatr
; 196: 154-160.e2, 2018 05.
Artigo
Inglês
| MEDLINE | ID: mdl-29395171
19.
Update on the safety and efficacy of retroviral gene therapy for immunodeficiency due to adenosine deaminase deficiency.
Blood
; 128(1): 45-54, 2016 07 07.
Artigo
Inglês
| MEDLINE | ID: mdl-27129325
20.
Intracellular Delivery of Human Purine Nucleoside Phosphorylase by Engineered Diphtheria Toxin Rescues Function in Target Cells.
Mol Pharm
; 15(11): 5217-5226, 2018 11 05.
Artigo
Inglês
| MEDLINE | ID: mdl-30212635