A novel HLA-DRB1 allele (DRB1*0417) in South American Indians

Acute mesenteric ischaemia in the elderly - results of combined endovascular and surgical treatment. Primary study.

Scientific reports·2025

Comparison of semi-quantitative and visual assessment of early MRI signal evolution in acute ischaemic stroke.

European journal of radiology open·2023

Endocrine system involvement in patients with RASopathies: A case series.

Frontiers in endocrinology·2022

Behçet disease, new insights in disease associations and manifestations: a next-generation sequencing study.

Clinical and experimental immunology·2021

How to proceed with a patent popliteal artery aneurysm below the chronic superficial femoral artery occlusion?

Rozhledy v chirurgii : mesicnik Ceskoslovenske chirurgicke spolecnosti·2020

Prophylactic bilateral iliac artery balloon occlusion during cesarean section in Jehova´s Witnesses patient.

Ceska gynekologie·2019

Intra-colony divergence and global allele sharing reflect purifying selection and recombination at the Botryllus histocompatibility factor locus.

Immunogenetics·2026

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Immunogenetics·2026

Genetic association of immunosenescence to immune decline.

Immunogenetics·2026

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Immunogenetics·2026

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Immunogenetics·2026

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Immunogenetics·2026

Assessing awareness toward genetic testing among patients with inherited retinal dystrophy in Japan.

Japanese journal of ophthalmology·2026

Integrated Molecular Autopsy in a Highly Consanguineous Perinatal Cohort With Severe Malformations and Strong Genetic Susceptibility.

Prenatal diagnosis·2026

The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

Experimental biology and medicine (Maywood, N.J.)·2026

A Protective Haplotype in trans Modifies Penetrance and Severity of TOR1A Dystonia.

medRxiv : the preprint server for health sciences·2026

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

Balkan medical journal·2026

Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

The Journal of allergy and clinical immunology·2026

Related Experiment Videos

A novel HLA-DRB1 allele (DRB1*0417) in South American Indians

Related Concept Videos

Acute mesenteric ischaemia in the elderly - results of combined endovascular and surgical treatment. Primary study.

Comparison of semi-quantitative and visual assessment of early MRI signal evolution in acute ischaemic stroke.

Endocrine system involvement in patients with RASopathies: A case series.

Behçet disease, new insights in disease associations and manifestations: a next-generation sequencing study.

How to proceed with a patent popliteal artery aneurysm below the chronic superficial femoral artery occlusion?

Prophylactic bilateral iliac artery balloon occlusion during cesarean section in Jehova´s Witnesses patient.

Intra-colony divergence and global allele sharing reflect purifying selection and recombination at the Botryllus histocompatibility factor locus.

Naïve adaptive immune receptor repertoires in celiac disease assessed by machine learning; impact of the HLA-DQ2.5 allotype on the TCR repertoire.

Genetic association of immunosenescence to immune decline.

Causal relationship and pathogenic mechanism analysis of breast cancer and coronary heart disease based on mendelian randomization and transcriptome data analysis.

Genotype-phenotype correlations in autoimmune and autoinflammatory diseases: An NGS-based immunogenetic cohort study.

Elevated interleukin-36γ and gene polymorphisms implicate novel risk in essential hypertension.

Assessing awareness toward genetic testing among patients with inherited retinal dystrophy in Japan.

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The causal relationship between antibody-mediated immune responses to infections and Graves' disease: a bi-directional Mendelian randomization analysis.

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A novel HLA-DRB1 allele (DRB1*0417) in South American Indians

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