Detalhe da pesquisa
1.
High resolution HLA analysis reveals independent class I haplotypes and amino-acid motifs protective for multiple sclerosis.
Genes Immun
; 20(4): 308-326, 2019 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29307888
2.
Correction: High resolution HLA analysis reveals independent class I haplotypes and amino-acid motifs protective for multiple sclerosis.
Genes Immun
; 20(4): 340, 2019 04.
Artigo
Inglês
| MEDLINE | ID: mdl-29915315
3.
Human NK cells licensed by killer Ig receptor genes have an altered cytokine program that modifies CD4+ T cell function.
J Immunol
; 193(2): 940-9, 2014 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-24935928
4.
A sequence-based approach demonstrates that balancing selection in classical human leukocyte antigen (HLA) loci is asymmetric.
Hum Mol Genet
; 22(2): 252-61, 2013 Jan 15.
Artigo
Inglês
| MEDLINE | ID: mdl-23065702
5.
Analysis of mixtures using next generation sequencing of mitochondrial DNA hypervariable regions.
Croat Med J
; 56(3): 208-17, 2015 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-26088845
6.
HLA-DP genetic variation, proxies for early life immune modulation and childhood acute lymphoblastic leukemia risk.
Blood
; 120(15): 3039-47, 2012 Oct 11.
Artigo
Inglês
| MEDLINE | ID: mdl-22923493
7.
HLA-C dysregulation as a possible mechanism of immune evasion in SARS-CoV-2 and other RNA-virus infections.
Front Immunol
; 13: 1011829, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-36325330
8.
Noninvasive Prenatal Test for ß-Thalassemia and Sickle Cell Disease Using Probe Capture Enrichment and Next-Generation Sequencing of DNA in Maternal Plasma.
J Appl Lab Med
; 7(2): 515-531, 2022 03 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34849992
9.
Juvenile idiopathic arthritis and HLA class I and class II interactions and age-at-onset effects.
Arthritis Rheum
; 62(6): 1781-91, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-20191588
10.
HLA genotyping in the international Type 1 Diabetes Genetics Consortium.
Clin Trials
; 7(1 Suppl): S75-87, 2010.
Artigo
Inglês
| MEDLINE | ID: mdl-20595243
11.
A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
Stroke
; 40(3): 683-95, 2009 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-19131662
12.
Defining multiple common "completely" conserved major histocompatibility complex SNP haplotypes.
Clin Immunol
; 132(2): 203-14, 2009 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-19427271
13.
Susceptibility to Crohn's disease is mediated by KIR2DL2/KIR2DL3 heterozygosity and the HLA-C ligand.
Immunogenetics
; 61(10): 663-71, 2009 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-19789864
14.
Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score.
Diabetes Care
; 42(3): 406-415, 2019 03.
Artigo
Inglês
| MEDLINE | ID: mdl-30659077
15.
Polymorphisms of the renin-angiotensin system genes predict progression of subclinical coronary atherosclerosis.
Diabetes
; 56(3): 863-71, 2007 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-17327458
16.
Type 1 diabetes risk for human leukocyte antigen (HLA)-DR3 haplotypes depends on genotypic context: association of DPB1 and HLA class I loci among DR3- and DR4-matched Italian patients and controls.
Hum Immunol
; 69(4-5): 291-300, 2008.
Artigo
Inglês
| MEDLINE | ID: mdl-18486765
17.
Alteration of cellular and humoral immunity by mutant p53 protein and processed mutant peptide in head and neck cancer.
Clin Cancer Res
; 13(23): 7199-206, 2007 Dec 01.
Artigo
Inglês
| MEDLINE | ID: mdl-18056201
18.
Correction: Shelly Y. Shih; et al.; Applications of Probe Capture Enrichment Next Generation Sequencing for Whole Mitochondrial Genome and 426 Nuclear SNPs for Forensically Challenging Samples. Genes 2018, 9, 49.
Genes (Basel)
; 9(2)2018 02 14.
Artigo
Inglês
| MEDLINE | ID: mdl-29443895
19.
Applications of Probe Capture Enrichment Next Generation Sequencing for Whole Mitochondrial Genome and 426 Nuclear SNPs for Forensically Challenging Samples.
Genes (Basel)
; 9(1)2018 Jan 22.
Artigo
Inglês
| MEDLINE | ID: mdl-29361782
20.
Polymorphism in the beta2-adrenergic receptor and lipoprotein lipase genes as risk determinants for idiopathic venous thromboembolism: a multilocus, population-based, prospective genetic analysis.
Circulation
; 113(18): 2193-200, 2006 May 09.
Artigo
Inglês
| MEDLINE | ID: mdl-16651467