Identification of a defective mouse immunoglobulin D (diversity) element which can undergo DJH, but not VHD, recombination

Genetic risk factors for type 2 diabetes with pharmacologic intervention in African-American patients with schizophrenia or schizoaffective disorder.

Schizophrenia research·2009

Cystatin B-deficient mice have increased expression of apoptosis and glial activation genes.

Human molecular genetics·2001

Nonequivalent nuclear location of immunoglobulin alleles in B lymphocytes.

Nature immunology·2001

From genes to proteins: high-throughput expression and purification of the human proteome.

Journal of cellular biochemistry·2000

Primary and secondary control-enhancing strategies: implications for health in later life.

Journal of aging and health·2000

CHD1 interacts with SSRP1 and depends on both its chromodomain and its ATPase/helicase-like domain for proper association with chromatin.

Chromosoma·1999

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

Reciprocal mediation of immuno-inflammation and insulin resistance in the risk of chronic kidney disease among patients with coronary artery disease: insights from neutrophil-to-lymphocyte ratio and triglyceride-glucose index.

Frontiers in immunology·2026

Defining the Genetic and Phenotypic Landscape of Primary Immune Regulatory Disorders Using the ClinGen Validation Framework.

medRxiv : the preprint server for health sciences·2026

Association of IFN-γ +874 T/A Polymorphism With COVID-19 Susceptibility, Severity, and Inflammatory Response: A Case-Control Study From Southern Iran.

Journal of clinical laboratory analysis·2026

Cardiac tamponade caused by effusive-constrictive pericarditis in a patient with common variable immunodeficiency: a case report.

International journal of emergency medicine·2026

CONFIRMATORY VALIDATION AND CLUSTER CLASSIFICATION OF THE IRRITABLE BOWEL SYNDROME SYMPTOM SEVERITY SCALE (IBS-SSS).

Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research·2026

Comparative serious infection and sepsis risks with advanced therapies in IMIDs: a Bayesian network meta-analysis.

The Journal of infection·2026

Related Experiment Videos

Identification of a defective mouse immunoglobulin D (diversity) element which can undergo DJH, but not VHD,

Related Concept Videos

Genetic risk factors for type 2 diabetes with pharmacologic intervention in African-American patients with schizophrenia or schizoaffective disorder.

Cystatin B-deficient mice have increased expression of apoptosis and glial activation genes.

Nonequivalent nuclear location of immunoglobulin alleles in B lymphocytes.

From genes to proteins: high-throughput expression and purification of the human proteome.

Primary and secondary control-enhancing strategies: implications for health in later life.

CHD1 interacts with SSRP1 and depends on both its chromodomain and its ATPase/helicase-like domain for proper association with chromatin.

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.

Reciprocal mediation of immuno-inflammation and insulin resistance in the risk of chronic kidney disease among patients with coronary artery disease: insights from neutrophil-to-lymphocyte ratio and triglyceride-glucose index.

Defining the Genetic and Phenotypic Landscape of Primary Immune Regulatory Disorders Using the ClinGen Validation Framework.

Association of IFN-γ +874 T/A Polymorphism With COVID-19 Susceptibility, Severity, and Inflammatory Response: A Case-Control Study From Southern Iran.

Cardiac tamponade caused by effusive-constrictive pericarditis in a patient with common variable immunodeficiency: a case report.

CONFIRMATORY VALIDATION AND CLUSTER CLASSIFICATION OF THE IRRITABLE BOWEL SYNDROME SYMPTOM SEVERITY SCALE (IBS-SSS).

Comparative serious infection and sepsis risks with advanced therapies in IMIDs: a Bayesian network meta-analysis.

Related Experiment Videos

Identification of a defective mouse immunoglobulin D (diversity) element which can undergo DJH, but not VHD,...

Related Concept Videos

Related Articles

Identification of a defective mouse immunoglobulin D (diversity) element which can undergo DJH, but not VHD,