A study of genetic markers in a family with polyendocrine disease

T cell phenotypes in patients with common variable immunodeficiency disorders: associations with clinical phenotypes in comparison with other groups with recurrent infections.

Clinical and experimental immunology·2012

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders.

Clinical and experimental immunology·2010

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

Nature genetics·2005

Measurement of peripheral B cell subpopulations in common variable immunodeficiency (CVID) using a whole blood method.

Clinical and experimental immunology·2005

Immunogenicity of routine vaccination against diphtheria, tetanus, and Haemophilus influenzae type b in Asian infants born in the United Kingdom.

Archives of disease in childhood·2005

Another cause of bloody diarrhoea in infancy: cytomegalovirus colitis in an immunocompetent child.

Journal of paediatrics and child health·2004

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

Yeast Knockout Strain Collection: Driving Functional Genomics, Biotechnological Applications and Human Disease Research.

Yeast (Chichester, England)·2026

Co-segregation of WFS1 p.Gly494Ser variant with recurrent vasovagal syncope in a multigenerational family: a candidate susceptibility variant needing independent validation.

Frontiers in pediatrics·2026

Chromosome painting in plants: history and future perspectives.

Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology·2026

A chromosome-scale genome of Capsicum pubescens provides insights into candidate terpene-associated gene clusters and pan variation of terpene synthases.

Planta·2026

Identification of Two Novel Compound Heterozygous ADAMTS17 Variants Associated With Weill-Marchesani Syndrome 4.

Laboratory investigation; a journal of technical methods and pathology·2026

Genomic inbreeding coefficients and inbreeding depression of semen production traits at genome-wide and chromosomal levels in Japanese Holstein bulls.

Journal of dairy science·2026

Related Experiment Videos

A study of genetic markers in a family with polyendocrine disease

Related Concept Videos

T cell phenotypes in patients with common variable immunodeficiency disorders: associations with clinical phenotypes in comparison with other groups with recurrent infections.

NOD2 polymorphisms in clinical phenotypes of common variable immunodeficiency disorders.

Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.

Measurement of peripheral B cell subpopulations in common variable immunodeficiency (CVID) using a whole blood method.

Immunogenicity of routine vaccination against diphtheria, tetanus, and Haemophilus influenzae type b in Asian infants born in the United Kingdom.

Another cause of bloody diarrhoea in infancy: cytomegalovirus colitis in an immunocompetent child.

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.

Yeast Knockout Strain Collection: Driving Functional Genomics, Biotechnological Applications and Human Disease Research.

Co-segregation of WFS1 p.Gly494Ser variant with recurrent vasovagal syncope in a multigenerational family: a candidate susceptibility variant needing independent validation.

Chromosome painting in plants: history and future perspectives.

A chromosome-scale genome of Capsicum pubescens provides insights into candidate terpene-associated gene clusters and pan variation of terpene synthases.

Identification of Two Novel Compound Heterozygous ADAMTS17 Variants Associated With Weill-Marchesani Syndrome 4.

Genomic inbreeding coefficients and inbreeding depression of semen production traits at genome-wide and chromosomal levels in Japanese Holstein bulls.

Related Experiment Videos

A study of genetic markers in a family with polyendocrine disease

Related Concept Videos

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