[Hodgkin's disease. Genetic factors or environmental factors?]

HLA-DRB1 and DQB1 allele distribution in the Muong population exposed to malaria in Vietnam.

Tissue antigens·2002

Hispano-Indian admixture in Paraguay studied by analysis of HLA-DRB1 polymorphism.

Pathologie-biologie·2002

HLA-DRB1 and DQB1 genotypes in patients with insulin-dependent neonatal diabetes mellitus. A study of 13 cases.

Tissue antigens·2000

A linkage disequilibrium map of the MHC region based on the analysis of 14 loci haplotypes in 50 French families.

European journal of human genetics : EJHG·2000

Mitochondrial DNA polymorphism in the Vietnamese population.

European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics·1999

[HLA-C allele recognition using DNA sequencing].

Pathologie-biologie·1999

Antibacterial and antibiofilm activities of Laurus nobilis L. essential oil against Staphylococcus aureus strains associated with oral infections.

Pathologie-biologie·2015

Oxidative damage and histopathological changes in lung of rat chronically exposed to nicotine alone or associated to ethanol.

Pathologie-biologie·2015

Biological diagnosis of diabetes mellitus.

Pathologie-biologie·2015

Association of CagPAI integrity with severeness of Helicobacter pylori infection in patients with gastritis.

Pathologie-biologie·2015

[Diagnostic performance of graphical anomalies in the detection of large platelets and platelet clumps].

Pathologie-biologie·2015

Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients.

Pathologie-biologie·2015

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

Stem cell research·2026

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Advanced science (Weinheim, Baden-Wurttemberg, Germany)·2026

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

CNS neuroscience & therapeutics·2026

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

International journal of molecular sciences·2026

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Genes·2026

Site-Resolved Plasma-Protein Architecture of Infection Susceptibility: A Cis-pQTL Mendelian Randomization and Colocalization Study.

Genes·2026

Related Experiment Videos

[Hodgkin's disease. Genetic factors or environmental factors?]

Related Concept Videos

HLA-DRB1 and DQB1 allele distribution in the Muong population exposed to malaria in Vietnam.

Hispano-Indian admixture in Paraguay studied by analysis of HLA-DRB1 polymorphism.

HLA-DRB1 and DQB1 genotypes in patients with insulin-dependent neonatal diabetes mellitus. A study of 13 cases.

A linkage disequilibrium map of the MHC region based on the analysis of 14 loci haplotypes in 50 French families.

Mitochondrial DNA polymorphism in the Vietnamese population.

[HLA-C allele recognition using DNA sequencing].

Antibacterial and antibiofilm activities of Laurus nobilis L. essential oil against Staphylococcus aureus strains associated with oral infections.

Oxidative damage and histopathological changes in lung of rat chronically exposed to nicotine alone or associated to ethanol.

Biological diagnosis of diabetes mellitus.

Association of CagPAI integrity with severeness of Helicobacter pylori infection in patients with gastritis.

[Diagnostic performance of graphical anomalies in the detection of large platelets and platelet clumps].

Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients.

Generation and characterization of an isogenic gene-corrected iPSC line CARIMi009-A-1 from a Hutchinson-Gilford Progeria Syndrome (HGPS) patient with a heterozygous G608G mutation in the LMNA gene.

A Rare De Novo Missense Mutation in IFT122 Confers a Genetic Susceptibility Factor of Idiopathic Pediatric Uveitis Via Trio-based Whole-Exome Sequencing.

Integrated Genomic and Proteomic Analysis Reveals T-B Lymphocyte Signatures in the MYCN Driven "Immune Desert" of Specific Neuroblastoma Subtypes.

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Site-Resolved Plasma-Protein Architecture of Infection Susceptibility: A Cis-pQTL Mendelian Randomization and Colocalization Study.

Related Experiment Videos

[Hodgkin's disease. Genetic factors or environmental factors?]

Related Concept Videos

Related Articles