Detalhe da pesquisa
1.
Adenoviral vectors infect B lymphocytes in vivo.
Mol Ther
; 31(9): 2600-2611, 2023 09 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37452494
2.
Correction of recessive dystrophic epidermolysis bullosa by homology-directed repair-mediated genome editing.
Mol Ther
; 29(6): 2008-2018, 2021 06 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33609734
3.
Gene therapy for primary immunodeficiency.
Hum Mol Genet
; 28(R1): R15-R23, 2019 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31297531
4.
Older Adults' Risk Perception during the COVID-19 Pandemic in Lombardy Region of Italy: A Cross-sectional Survey.
J Gerontol Soc Work
; 64(6): 585-598, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-33393447
5.
NEIL1 is a candidate gene associated with common variable immunodeficiency in a patient with a chromosome 15q24 deletion.
Clin Immunol
; 176: 71-76, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28093361
6.
Comparison of imported Plasmodium ovale curtisi and P. ovale wallikeri infections among patients in Spain, 2005-2011.
Emerg Infect Dis
; 20(3): 409-16, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24572501
7.
Human skin-derived keratinocytes and fibroblasts co-cultured on 3D poly ε-caprolactone scaffold support in vitro HSC differentiation into T-lineage committed cells.
Int Immunol
; 25(12): 703-14, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24038600
8.
Role of the common γ chain in cell cycle progression of human malignant cell lines.
Int Immunol
; 24(3): 159-67, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22223761
9.
De novo 13q12.3-q14.11 deletion involving BRCA2 gene in a patient with developmental delay, elevated IgM levels, transient ataxia, and cerebellar hypoplasia, mimicking an A-T like phenotype.
Am J Med Genet A
; 158A(10): 2571-6, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22903806
10.
From murine to human nude/SCID: the thymus, T-cell development and the missing link.
Clin Dev Immunol
; 2012: 467101, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22474479
11.
Social Network and Environment as Determinants of Disability and Quality of Life in Aging: Results From an Italian Study.
Front Med (Lausanne)
; 9: 854779, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35677824
12.
A Novel SPINK5 Gene Mutation Associated with Netherton Syndrome in an Omani Patient.
Sultan Qaboos Univ Med J
; 21(4): 652-656, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34888090
13.
BHLHE40 Regulates IL-10 and IFN-γ Production in T Cells but Does Not Interfere With Human Type 1 Regulatory T Cell Differentiation.
Front Immunol
; 12: 683680, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34305917
14.
Identification of preexisting adaptive immunity to Cas9 proteins in humans.
Nat Med
; 25(2): 249-254, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30692695
15.
Highly Efficient and Marker-free Genome Editing of Human Pluripotent Stem Cells by CRISPR-Cas9 RNP and AAV6 Donor-Mediated Homologous Recombination.
Cell Stem Cell
; 24(5): 821-828.e5, 2019 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31051134
16.
Creating a Culture of Health in Planning and Implementing Innovative Strategies Addressing Non-communicable Chronic Diseases.
Front Sociol
; 4: 9, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-33869336
17.
Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency.
J Exp Med
; 214(1): 91-106, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28011864
18.
In this issue: FOX genes and the immune response.
Int Rev Immunol
; 33(2): 81-2, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24621091
19.
FOXN1 in organ development and human diseases.
Int Rev Immunol
; 33(2): 83-93, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24432845
20.
FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program.
Front Immunol
; 4: 187, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23874334