The gene encoding the Ia-associated invariant chain is located on chromosome 18 in the mouse

NK- and CD8(+) T cell-mediated eradication of established tumors by peritumoral injection of CpG-containing oligodeoxynucleotides.

Journal of immunology (Baltimore, Md. : 1950)·2001

SRbeta coordinates signal sequence release from SRP with ribosome binding to the translocon.

The EMBO journal·2001

Conformational alterations during biosynthesis of HLA-DR3 molecules controlled by invariant chain and HLA-DM.

European journal of immunology·2001

Prion protein contains a second endoplasmic reticulum targeting signal sequence located at its C terminus.

The Journal of biological chemistry·2001

Impaired immune responses and altered peptide repertoire in tapasin-deficient mice.

Nature immunology·2001

Export of antigenic peptides from the endoplasmic reticulum intersects with retrograde protein translocation through the Sec61p channel.

Immunity·2000

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

Identification of COPZ1 as a Shared Candidate Ferroptosis-Related Hub Gene in Periodontitis and Inflammatory Bowel Disease.

Human mutation·2026

From Undifferentiated Connective Tissue Disease to Common Variable Immunodeficiency: A Novel NFKB1 Mutation in a Pediatric Case.

Clinical case reports·2026

Comparison of pre-treatment 68Ga-DOTA-WL12 and 18F-FDG uptake in predicting response to chemo-immunotherapy in head and neck squamous cell carcinoma.

European radiology·2026

Minimally Invasive Surgical Treatment of Different Types of Hyperinsulinism.

Journal of pediatric surgery·2026

Gastric mucosa intestinal metaplasia segmentation and grading via transformer-CNN fusion architecture: an interpretable digital pathology diagnostic framework.

Medical & biological engineering & computing·2026

Invasive carcinoma ex intraductal carcinoma of the salivary gland showing extensive infiltrative growth despite deceptively low-grade cribriform morphology.

Virchows Archiv : an international journal of pathology·2026

Related Experiment Videos

The gene encoding the Ia-associated invariant chain is located on chromosome 18 in the mouse

Related Concept Videos

NK- and CD8(+) T cell-mediated eradication of established tumors by peritumoral injection of CpG-containing oligodeoxynucleotides.

SRbeta coordinates signal sequence release from SRP with ribosome binding to the translocon.

Conformational alterations during biosynthesis of HLA-DR3 molecules controlled by invariant chain and HLA-DM.

Prion protein contains a second endoplasmic reticulum targeting signal sequence located at its C terminus.

Impaired immune responses and altered peptide repertoire in tapasin-deficient mice.

Export of antigenic peptides from the endoplasmic reticulum intersects with retrograde protein translocation through the Sec61p channel.

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.

Identification of COPZ1 as a Shared Candidate Ferroptosis-Related Hub Gene in Periodontitis and Inflammatory Bowel Disease.

From Undifferentiated Connective Tissue Disease to Common Variable Immunodeficiency: A Novel NFKB1 Mutation in a Pediatric Case.

Comparison of pre-treatment 68Ga-DOTA-WL12 and 18F-FDG uptake in predicting response to chemo-immunotherapy in head and neck squamous cell carcinoma.

Minimally Invasive Surgical Treatment of Different Types of Hyperinsulinism.

Gastric mucosa intestinal metaplasia segmentation and grading via transformer-CNN fusion architecture: an interpretable digital pathology diagnostic framework.

Invasive carcinoma ex intraductal carcinoma of the salivary gland showing extensive infiltrative growth despite deceptively low-grade cribriform morphology.

Related Experiment Videos

The gene encoding the Ia-associated invariant chain is located on chromosome 18 in the mouse

Abstract:

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