A study of red cell adenosine deaminase (ADA) types in 116 Danish families

Significant effect of high-resolution HLA-DRB1 matching in high-risk corneal transplantation.

Transplantation·1996

Interplay between promoter and structural gene variants control basal serum level of mannan-binding protein.

Journal of immunology (Baltimore, Md. : 1950)·1995

Antigenic characteristics and cDNA sequences of HLA-B73.

European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics·1995

Cancer risk after renal transplantation in the Nordic countries, 1964-1986.

International journal of cancer·1995

[Scandiatransplant].

Nordisk medicin·1994

A new frequent allele is the missing link in the structural polymorphism of the human mannan-binding protein.

Immunogenetics·1994

A frequentist test of proportional colocalization after selecting relevant genetic variants.

Human heredity·2026

Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk.

Human heredity·2026

Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang.

Human heredity·2026

Erratum.

Human heredity·2026

Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population.

Human heredity·2025

Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI.

Human heredity·2025

Quantifying genetic load through joint modelling of inbreeding depression and inbreeding load for litter size in rabbits.

Genetics, selection, evolution : GSE·2026

Whole genome duplication through mitotic slippage causes nuclear instability.

The EMBO journal·2026

Divergent microtubule-organizing center strategies in mammalian gametogenesis.

Trends open·2026

Analytical evaluation and method comparison of an orexin-A radioimmunoassay in cerebrospinal fluid: establishing a cut-off value for type 1 narcolepsy and exploring genetic and clinical characteristics.

Sleep medicine·2026

Highly Contiguous Is Not Chromosomally Accurate: Integrated Cytogenetic and Genomic Mapping in Two Turtle Genome.

The Journal of heredity·2026

Ophthalmic Manifestations in A Patient With Kabuki Syndrome: A Case Report With a KDM6A Gene Variant.

Case reports in ophthalmological medicine·2026

Related Experiment Videos

A study of red cell adenosine deaminase (ADA) types in 116 Danish families

Related Concept Videos

Significant effect of high-resolution HLA-DRB1 matching in high-risk corneal transplantation.

Interplay between promoter and structural gene variants control basal serum level of mannan-binding protein.

Antigenic characteristics and cDNA sequences of HLA-B73.

Cancer risk after renal transplantation in the Nordic countries, 1964-1986.

[Scandiatransplant].

A new frequent allele is the missing link in the structural polymorphism of the human mannan-binding protein.

A frequentist test of proportional colocalization after selecting relevant genetic variants.

Investigation of the Effects of Noncoding LDLR Variants on Hyperlipidaemia risk.

Comparative Profiles of Pediatric Mendeliome: A Single-Center 572-Whole-Exome Sequencing Study in Xinjiang.

Erratum.

Exploratory Analysis of HMGB1 Genetic Variants and Their Potential Association with Lung Cancer Susceptibility and Chemotherapy Response in a Chinese Population.

Weighted Burden Analysis of Rare Genetic Variants Identifies Novel Genes with Effects on BMI.

Quantifying genetic load through joint modelling of inbreeding depression and inbreeding load for litter size in rabbits.

Whole genome duplication through mitotic slippage causes nuclear instability.

Divergent microtubule-organizing center strategies in mammalian gametogenesis.

Analytical evaluation and method comparison of an orexin-A radioimmunoassay in cerebrospinal fluid: establishing a cut-off value for type 1 narcolepsy and exploring genetic and clinical characteristics.

Highly Contiguous Is Not Chromosomally Accurate: Integrated Cytogenetic and Genomic Mapping in Two Turtle Genome.

Ophthalmic Manifestations in A Patient With Kabuki Syndrome: A Case Report With a KDM6A Gene Variant.

Related Experiment Videos

A study of red cell adenosine deaminase (ADA) types in 116 Danish families

Related Concept Videos

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