A linkage study of rabbit serum high density lipoprotein (HDL) allotypes

Detection of mutations by single-strand conformation polymorphism (SSCP) analysis and SSCP-hybrid methods.

Current protocols in human genetics·2008

Mutations in exons 5-8 of the p53 gene, independent of their type and location, are associated with increased apoptosis and mitosis in invasive breast carcinoma.

The Journal of pathology·2000

GSTM1 and NAT2 polymorphisms in operable and non-operable lung cancer patients.

Carcinogenesis·1999

Relationship between abnormal p53 protein and failure to express p21 protein in human breast carcinomas.

The Journal of pathology·1997

A segregation analysis of testicular cancer based on Norwegian and Swedish families.

British journal of cancer·1997

Specific P53 mutations are associated with de novo resistance to doxorubicin in breast cancer patients.

Nature medicine·1996

VHDJH to JH joining is not blocked in mu-chain-producing pre-B cells, implying the breakdown of allelic exclusion.

Journal of immunogenetics·1990

Characterization of soluble HLA molecules in sweat and quantitative HLA differences in serum of healthy individuals.

Journal of immunogenetics·1990

Characterization of MHC ancestral haplotypes associated with insulin-dependent diabetes mellitus: evidence for involvement of non-HLA genes.

Journal of immunogenetics·1990

Increased interleukin-2 receptor affinity in normal HLA A1 B8 DR3 subjects.

Journal of immunogenetics·1990

Immunogenetic aspects of human thyroglobulin-reactive T cell lines and hybridomas.

Journal of immunogenetics·1990

Evidence against extended DR3-related haplotypes in Graves' disease.

Journal of immunogenetics·1990

Measuring canine impulsivity: translation and validation of a German dog impulsivity assessment scale.

Frontiers in veterinary science·2026

Hyperinsulinism-hyperammonemia syndrome due to an autosomal dominant GLUD1 p.Ile497Met mutation.

JCEM case reports·2026

Conservation and plasticity in avian prepro-GnRH-I reflect a modular evolutionary architecture.

General and comparative endocrinology·2026

Single-cell multiomic mapping of genetic predisposition to childhood B-cell acute lymphoblastic leukemia.

bioRxiv : the preprint server for biology·2026

Identifying the causal allele in the CD40 autoimmune locus enables discovery of context-specific trans-effects in B cells.

bioRxiv : the preprint server for biology·2026

Shared genetic architecture between Crohn's disease and IgA nephropathy: implications for a gut-immune-kidney axis.

Frontiers in immunology·2026

Related Experiment Videos

A linkage study of rabbit serum high density lipoprotein (HDL) allotypes

Related Concept Videos

Detection of mutations by single-strand conformation polymorphism (SSCP) analysis and SSCP-hybrid methods.

Mutations in exons 5-8 of the p53 gene, independent of their type and location, are associated with increased apoptosis and mitosis in invasive breast carcinoma.

GSTM1 and NAT2 polymorphisms in operable and non-operable lung cancer patients.

Relationship between abnormal p53 protein and failure to express p21 protein in human breast carcinomas.

A segregation analysis of testicular cancer based on Norwegian and Swedish families.

Specific P53 mutations are associated with de novo resistance to doxorubicin in breast cancer patients.

VHDJH to JH joining is not blocked in mu-chain-producing pre-B cells, implying the breakdown of allelic exclusion.

Characterization of soluble HLA molecules in sweat and quantitative HLA differences in serum of healthy individuals.

Characterization of MHC ancestral haplotypes associated with insulin-dependent diabetes mellitus: evidence for involvement of non-HLA genes.

Increased interleukin-2 receptor affinity in normal HLA A1 B8 DR3 subjects.

Immunogenetic aspects of human thyroglobulin-reactive T cell lines and hybridomas.

Evidence against extended DR3-related haplotypes in Graves' disease.

Measuring canine impulsivity: translation and validation of a German dog impulsivity assessment scale.

Hyperinsulinism-hyperammonemia syndrome due to an autosomal dominant GLUD1 p.Ile497Met mutation.

Conservation and plasticity in avian prepro-GnRH-I reflect a modular evolutionary architecture.

Single-cell multiomic mapping of genetic predisposition to childhood B-cell acute lymphoblastic leukemia.

Identifying the causal allele in the CD40 autoimmune locus enables discovery of context-specific trans-effects in B cells.

Shared genetic architecture between Crohn's disease and IgA nephropathy: implications for a gut-immune-kidney axis.

Related Experiment Videos

A linkage study of rabbit serum high density lipoprotein (HDL) allotypes

Abstract:

Related Concept Videos

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