HL-A haplotype frequencies in Denmark and Norway

The HLA-DP2 protein binds the immunodominant epitope from myelin basic protein, MBP85-99, with high affinity.

Tissue antigens·2011

Neonatal Immune Thrombocytopenia Due to Allo-or Autoantibodies: Clinical and Immunological Analysis of 83 Cases.

Platelets·2010

An update to HLA nomenclature, 2010.

Bone marrow transplantation·2010

Identification of new sensitive biomarkers for the in vivo response to interferon-beta treatment in multiple sclerosis using DNA-array evaluation.

European journal of neurology·2009

Gene expression analysis of interferon-beta treatment in multiple sclerosis.

Multiple sclerosis (Houndmills, Basingstoke, England)·2008

Haematopoietic cell transplantation with non-myeloablative conditioning in Denmark: disease-specific outcome, complications and hospitalization requirements of the first 100 transplants.

Bone marrow transplantation·2008

Four amino acid exchanges located in the alpha-2 domain specify the novel HLA-B*50:20 allele.

Tissue antigens·2015

A novel HLA-A02 variant, HLA-A02:575, detected in a Taiwanese bone marrow hematopoietic stem cell donor.

Tissue antigens·2015

Identification of a novel HLA-A*02:06:01:02 allele in a Chinese individual by sequence-based typing.

Tissue antigens·2015

Genetic variation of the MHC class II DRB genes in the Japanese weasel, Mustela itatsi, endemic to Japan, compared with the Siberian weasel, Mustela sibirica.

Tissue antigens·2015

Questionable expression of unstable DQ heterodimer containing HLA-DQA1*01:07.

Tissue antigens·2015

Characterization of bovine MHC class II DRB3 diversity in South American Holstein cattle populations.

Tissue antigens·2015

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Bioinformatics (Oxford, England)·2026

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Drug metabolism and personalized therapy·2026

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

Current medicinal chemistry·2026

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

American journal of medical genetics. Part A·2026

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Human mutation·2026

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

iScience·2026

Related Experiment Videos

HL-A haplotype frequencies in Denmark and Norway

Related Concept Videos

The HLA-DP2 protein binds the immunodominant epitope from myelin basic protein, MBP85-99, with high affinity.

Neonatal Immune Thrombocytopenia Due to Allo-or Autoantibodies: Clinical and Immunological Analysis of 83 Cases.

An update to HLA nomenclature, 2010.

Identification of new sensitive biomarkers for the in vivo response to interferon-beta treatment in multiple sclerosis using DNA-array evaluation.

Gene expression analysis of interferon-beta treatment in multiple sclerosis.

Haematopoietic cell transplantation with non-myeloablative conditioning in Denmark: disease-specific outcome, complications and hospitalization requirements of the first 100 transplants.

Four amino acid exchanges located in the alpha-2 domain specify the novel HLA-B*50:20 allele.

A novel HLA-A02 variant, HLA-A02:575, detected in a Taiwanese bone marrow hematopoietic stem cell donor.

Identification of a novel HLA-A*02:06:01:02 allele in a Chinese individual by sequence-based typing.

Genetic variation of the MHC class II DRB genes in the Japanese weasel, Mustela itatsi, endemic to Japan, compared with the Siberian weasel, Mustela sibirica.

Questionable expression of unstable DQ heterodimer containing HLA-DQA1*01:07.

Characterization of bovine MHC class II DRB3 diversity in South American Holstein cattle populations.

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

Related Experiment Videos

HL-A haplotype frequencies in Denmark and Norway

Related Concept Videos

Related Articles