Detalhe da pesquisa
1.
Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.
J Clin Immunol
; 44(2): 42, 2024 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-38231436
2.
In-silico assessment of high-risk non-synonymous SNPs in ADAMTS3 gene associated with Hennekam syndrome and their impact on protein stability and function.
BMC Bioinformatics
; 24(1): 251, 2023 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37322437
3.
In Silico Analysis Revealed Five Novel High-Risk Single-Nucleotide Polymorphisms (rs200384291, rs201163886, rs193141883, rs201139487, and rs201723157) in ELANE Gene Causing Autosomal Dominant Severe Congenital Neutropenia 1 and Cyclic Hematopoiesis.
ScientificWorldJournal
; 2022: 3356835, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35571273
4.
Identification of The Immune Subtype Among Muscle-invasive Bladder Cancer Patients by Multiple Datasets.
Acta Med Indones
; 54(1): 62-71, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-35398827
5.
Defining muscle-invasive bladder cancer immunotypes by introducing tumor mutation burden, CD8+ T cells, and molecular subtypes.
Hereditas
; 158(1): 1, 2021 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33388091
6.
Predicting the Most Deleterious Missense Nonsynonymous Single-Nucleotide Polymorphisms of Hennekam Syndrome-Causing CCBE1 Gene, In Silico Analysis.
ScientificWorldJournal
; 2021: 6642626, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34234628
7.
Correction to: Clinical and Treatment History of Patients with Partial DiGeorge Syndrome and Autoimmune Cytopenia at Multiple Centers.
J Clin Immunol
; 44(3): 72, 2024 Feb 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38421526
8.
A co-expression network for differentially expressed genes in bladder cancer and a risk score model for predicting survival.
Hereditas
; 156: 24, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31333338
9.
The J Daughter Siberia Project.
J Clin Immunol
; 41(1): 262-265, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33078350
10.
Health-related quality of life in patients with inborn errors of immunity: a bibliometric analysis.
Front Immunol
; 15: 1371124, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38515759
11.
The spread of the J Project.
J Clin Immunol
; 33(6): 1037-42, 2013 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23686437
12.
Novel Disease-Associated Missense Single-Nucleotide Polymorphisms Variants Predication by Algorithms Tools and Molecular Dynamics Simulation of Human TCIRG1 Gene Causing Congenital Neutropenia and Osteopetrosis.
Front Mol Biosci
; 9: 879875, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35573728
13.
Newborn Screening through TREC, TREC/KREC System for Primary Immunodeficiency with limitation of TREC/KREC. Comprehensive Review.
Antiinflamm Antiallergy Agents Med Chem
; 20(2): 132-149, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-32748762
14.
Efficacy and safety of octanorm (cutaquig®) in adults with primary immunodeficiencies with predominant antibody deficiency: a prospective, open-label study.
Immunotherapy
; 12(5): 299-309, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32212944
15.
Geographical Distribution, Incidence, Malignancies, and Outcome of 136 Eastern Slavic Patients With Nijmegen Breakage Syndrome and NBN Founder Variant c.657_661del5.
Front Immunol
; 11: 602482, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33488600
16.
Primary Immunodeficiencies in Russia: Data From the National Registry.
Front Immunol
; 11: 1491, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32849507
17.
Editorial: Advances in primary immunodeficiencies (inborn errors of immunity) in Central-Eastern Europe, volume II.
Front Immunol
; 14: 1221137, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37383230
18.
Identification of miR-200c and miR141-Mediated lncRNA-mRNA Crosstalks in Muscle-Invasive Bladder Cancer Subtypes.
Front Genet
; 9: 422, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30323832
19.
Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication.
Front Immunol
; 8: 685, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28952612