Detalhe da pesquisa
1.
A longitudinal characterization of the adaptive and behavioral profile in Sotos syndrome.
Am J Med Genet A
; 194(6): e63553, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38318994
2.
Cognitive, adaptive and behavioral profile in Sotos syndrome children with 5q35 microdeletion or intragenic variants.
Am J Med Genet A
; 191(7): 1836-1848, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37066965
3.
CD20-Mimotope Peptides: A Model to Define the Molecular Basis of Epitope Spreading.
Int J Mol Sci
; 20(8)2019 Apr 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-31003532
4.
Sleep disturbances and behavioral symptoms in pediatric Sotos syndrome.
Front Neurol
; 15: 1360055, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38434199
5.
Generation of IGGi003-A induced pluripotent stem cell line from a patient with Sotos Syndrome carrying c.1633delA NSD1 variant in exon 5.
Stem Cell Res
; 76: 103324, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38301425
6.
CD39 is highly involved in mediating the suppression activity of tumor-infiltrating CD8+ T regulatory lymphocytes.
Cancer Immunol Immunother
; 62(5): 851-62, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23359087
7.
Comparative analysis of cancer vaccine settings for the selection of an effective protocol in mice.
J Transl Med
; 11: 120, 2013 May 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-23663506
8.
Molecular Analysis and Reclassification of NSD1 Gene Variants in a Cohort of Patients with Clinical Suspicion of Sotos Syndrome.
Genes (Basel)
; 14(2)2023 01 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-36833222
9.
Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion.
Stem Cell Res
; 66: 103007, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36580887
10.
Identification of alternative transcripts of NSD1 gene in Sotos Syndrome patients and healthy subjects.
Gene
; 851: 146970, 2023 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36261088
11.
Exome Analysis Reveals Novel Missense and Deletion Variants in the CC2D2A Gene as Causative of Joubert Syndrome.
Genes (Basel)
; 14(4)2023 03 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37107568
12.
NSD1 Mutations in Sotos Syndrome Induce Differential Expression of Long Noncoding RNAs, miR646 and Genes Controlling the G2/M Checkpoint.
Life (Basel)
; 12(7)2022 Jul 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35888078
13.
Alteration of Th17 and Treg cell subpopulations co-exist in patients affected with systemic sclerosis.
Clin Immunol
; 139(3): 249-57, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21419712
14.
Beyond APECED: An update on the role of the autoimmune regulator gene (AIRE) in physiology and disease.
Autoimmun Rev
; 17(4): 325-330, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29427825
15.
Azacytidine mitigates experimental sclerodermic chronic graft-versus-host disease.
J Hematol Oncol
; 9(1): 53, 2016 07 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-27377819
16.
Residual tumor micro-foci and overwhelming regulatory T lymphocyte infiltration are the causes of bladder cancer recurrence.
Oncotarget
; 7(6): 6424-35, 2016 Feb 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26824503
17.
AIRE polymorphism, melanoma antigen-specific T cell immunity, and susceptibility to melanoma.
Oncotarget
; 7(38): 60872-60884, 2016 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27563821
18.
Indoleamine 2,3 dioxygenase gene polymorphisms correlate with CD8+ Treg impairment in systemic sclerosis.
Hum Immunol
; 74(2): 166-9, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23200754
19.
Cyclophosphamide inhibits the generation and function of CD8(+) regulatory T cells.
Hum Immunol
; 73(3): 207-13, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22285846