Detalhe da pesquisa
1.
Paroxysmal Movement Disorders: Recent Advances.
Curr Neurol Neurosci Rep;
19(7): 48, 2019 06 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31187296
2.
Novel genetic loci associated HLA-B*08:01 positive myasthenia gravis.
J Autoimmun;
88: 43-49, 2018 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29037440
3.
Targeted next-generation sequencing for genetic diagnosis of 160 patients with primary immunodeficiency in south China.
Pediatr Allergy Immunol;
29(8): 863-872, 2018 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30152884
4.
Next Generation Sequencing Data Analysis in Primary Immunodeficiency Disorders - Future Directions.
J Clin Immunol;
36 Suppl 1: 68-75, 2016 05.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26993986
5.
Reversal of Immunoglobulin A Deficiency in Children.
J Clin Immunol;
35(1): 87-91, 2015 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25370723
6.
Genetic interrogation for sequence and copy number variants in systemic lupus erythematosus.
Front Genet;
15: 1341272, 2024.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38501057
7.
Serum methylation levels of TAC1. SEPT9 and EYA4 as diagnostic markers for early colorectal cancers: a pilot study.
Biomarkers;
18(5): 399-405, 2013 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23862763
8.
STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency.
Front Genet;
12: 736235, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34976003
9.
Histocompatibility Complex Status and Mendelian Randomization Analysis in Unsolved Antibody Deficiency.
Front Immunol;
11: 14, 2020.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32038658
10.
IL2RG hypomorphic mutation: identification of a novel pathogenic mutation in exon 8 and a review of the literature.
Allergy Asthma Clin Immunol;
15: 2, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30622570
11.
Study of gene expression profile during cord blood-associated megakaryopoiesis.
Eur J Haematol;
81(3): 196-208, 2008 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18510698
12.
Tuberculosis and impaired IL-23-dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant.
Sci Immunol;
3(30)2018 12 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30578352
13.
The effects of different travel modes and travel destinations on COVID-19 transmission in global cities.
Sci Bull (Beijing);
67(6): 588-592, 2022 Mar 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34868708
14.
Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome.
J Exp Med;
212(10): 1641-62, 2015 Sep 21.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26304966
15.
Comparison of 7 methods for extracting cell-free DNA from serum samples of colorectal cancer patients.
Clin Chem;
55(3): 587-9, 2009 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19246404
16.
Keloid fibroblasts are more sensitive to Wnt3a treatment in terms of elevated cellular growth and fibronectin expression.
J Dermatol Sci;
64(3): 199-209, 2011 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22005028
17.
Studies of Wilms' Tumor (WT1) Gene Expression in Adult Acute Leukemias in Singapore.
Biomark Insights;
2: 293-8, 2007 Aug 08.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19662212