Age and genetic influence on immunity in NZB and autoimmune-resistant mice

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Possible role of natural killer cells in pemphigus vulgaris - preliminary observations.

Clinical and experimental immunology·2008

Allele frequencies for 15 autosomal STR loci and admixture estimates in Puerto Rican Americans.

Forensic science international·2006

HLA-Cw0409N is associated with HLA-A2301 and HLA-B*4403-carrying haplotypes.

Human immunology·2004

Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks.

Tissue antigens·2003

TNF-alpha promoter single nucleotide polymorphisms are markers of human ancestry.

Genes and immunity·2002

D-penicillamine-induced pancreatic islet autoantibody production is independent of the immunogenetic background: a lesson from patients with Wilson's disease.

Clinical immunology and immunopathology·1998

Characterization of gastric Na+/I- symporter of the rat.

Clinical immunology and immunopathology·1998

CD8(+), radiosensitive T cells of parental origin, oppose cells capable of down-regulating cytotoxicity in murine acute lethal graft-versus-host disease.

Clinical immunology and immunopathology·1998

Specific activity of alpha1proteinase inhibitor and alpha2macroglobulin in human serum: application to insulin-dependent diabetes mellitus.

Clinical immunology and immunopathology·1998

Somatic hypermutation in T-independent and T-dependent immune responses to Haemophilus influenzae type b polysaccharide.

Clinical immunology and immunopathology·1998

Treatment with progesterone analogues decreases macrophage Fcgamma receptors expression.

Clinical immunology and immunopathology·1998

The role of ferroptosis in juvenile idiopathic arthritis: Causal inference and mediation by immune phenotypes.

Medicine·2026

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

Related Experiment Videos

Age and genetic influence on immunity in NZB and autoimmune-resistant mice

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Strategies and technical challenges in allele level Class II typing in 2578 bone marrow transplantation donor-recipient pairs.

Possible role of natural killer cells in pemphigus vulgaris - preliminary observations.

Allele frequencies for 15 autosomal STR loci and admixture estimates in Puerto Rican Americans.

HLA-Cw0409N is associated with HLA-A2301 and HLA-B*4403-carrying haplotypes.

Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks.

TNF-alpha promoter single nucleotide polymorphisms are markers of human ancestry.

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Specific activity of alpha1proteinase inhibitor and alpha2macroglobulin in human serum: application to insulin-dependent diabetes mellitus.

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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.

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Age and genetic influence on immunity in NZB and autoimmune-resistant mice

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