Detalhe da pesquisa
1.
Outcomes of hematopoietic stem cell gene therapy for Wiskott-Aldrich syndrome.
Blood
; 142(15): 1281-1296, 2023 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37478401
2.
Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation.
PLoS Genet
; 15(2): e1007917, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30707697
3.
Neonatal-Onset Chronic Diarrhea Caused by Homozygous Nonsense WNT2B Mutations.
Am J Hum Genet
; 103(1): 131-137, 2018 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29909964
4.
Primary immunodeficiency testing in a Massachusetts tertiary care NICU: persistent challenges in the extremely premature population.
Pediatr Res
; 89(3): 549-553, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32268342
5.
Hypersensitivity to tetracyclines: Skin testing, graded challenge, and desensitization regimens.
Ann Allergy Asthma Immunol
; 124(6): 589-593, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32087343
6.
Risk-factors Associated With Poor Outcomes in VEO-IBD Secondary to XIAP Deficiency: A Case Report and Literature Review.
J Pediatr Gastroenterol Nutr
; 69(1): e13-e18, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31232887
7.
Applying the bronchopulmonary dysplasia framework to necrotizing enterocolitis.
Front Pediatr
; 12: 1388392, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38813544
8.
WNT2B Deficiency Causes Enhanced Susceptibility to Colitis Due to Increased Inflammatory Cytokine Production.
Cell Mol Gastroenterol Hepatol
; 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38697357
9.
Human and mouse macrophages collaborate with neutrophils to kill larval Strongyloides stercoralis.
Infect Immun
; 81(9): 3346-55, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23798541
10.
M1 and M2 Macrophages Differentially Regulate Colonic Crypt Renewal.
Inflamm Bowel Dis
; 2023 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38001043
11.
A sepsis trigger tool reduces time to antibiotic administration in the NICU.
J Perinatol
; 43(6): 806-812, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36813901
12.
Ectopic Rod Photoreceptor Development in Mice with Genetic Deficiency of WNT2B.
Cells
; 12(7)2023 03 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37048106
13.
Antimicrobial peptides modulate lung injury by altering the intestinal microbiota.
bioRxiv
; 2023 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36993189
14.
Antimicrobial peptides modulate lung injury by altering the intestinal microbiota.
Microbiome
; 11(1): 226, 2023 10 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-37845716
15.
WNT2B Deficiency Causes Increased Susceptibility to Colitis in Mice and Impairs Intestinal Epithelial Development in Humans.
bioRxiv
; 2023 Apr 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-37131772
16.
Premature Infants Have Normal Maturation of the T Cell Receptor Repertoire at Term.
Front Immunol
; 13: 854414, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35707545
17.
Insights into the Role of Commensal-Specific T Cells in Intestinal Inflammation.
J Inflamm Res
; 15: 1873-1887, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35342295
18.
Major basic protein from eosinophils and myeloperoxidase from neutrophils are required for protective immunity to Strongyloides stercoralis in mice.
Infect Immun
; 79(7): 2770-8, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21482685
19.
Inborn Errors of Immunity in the Premature Infant: Challenges in Recognition and Diagnosis.
Front Immunol
; 12: 758373, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-35003071
20.
Novel variants in the stem cell niche factor WNT2B define the disease phenotype as a congenital enteropathy with ocular dysgenesis.
Eur J Hum Genet
; 29(6): 998-1007, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33526876