Association between atopic asthma and a coding variant of Fc epsilon RI beta in a Japanese population

A rare partnership: patient community and industry collaboration to shape the impact of real-world evidence on the rare disease ecosystem.

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Immune and genetic aspects of asthma, allergy and parasitic worm infections: evolutionary links.

Parasite immunology·2009

PTPRC (CD45) variation and disease association studied using single nucleotide polymorphism tagging.

Tissue antigens·2008

The next extreme sport? Subdural haematoma in a patient with arachnoid cyst after head shaking competition.

British journal of neurosurgery·2006

Service provision of complex mutation analysis: a technical and economic appraisal using dystrophin point mutation analysis as an example.

Clinical genetics·2002

Use of Gore-Tex tubing as a conduit for inferior alveolar and lingual nerve repair: experience with 6 cases.

Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons·2001

Molecular basis of mucopolysaccharidosis IVA in a large cohort: genotype-phenotype correlations and reporting of 12 novel GALNS variants.

Human molecular genetics·2026

Shared genetic architecture of schizophrenia and lupus identifies pleiotropic loci with distinct downstream mechanisms.

Human molecular genetics·2026

Motor dysfunction phenotypes in a drosophila model validate DAO as an ALS gene.

Human molecular genetics·2026

Tissue-specific models of spinal muscular atrophy identify muscle functions required for Drosophila neuromuscular junction architecture.

Human molecular genetics·2026

Deep phenotyping of EHMT1 ankyrin repeat domain missense variants in Kleefstra syndrome by multi-tiered structural genomics analyses at atomic resolution.

Human molecular genetics·2026

MEF2C promoter variants in patent ductus arteriosus: a genetic and functional study.

Human molecular genetics·2026

Identification of Variants in Two Families With Congenital Cataract by Whole Exome Sequencing.

Molecular genetics & genomic medicine·2026

Golgi dysfunction in Alzheimer disease: from human multiomic signatures to therapeutic targets.

Experimental & molecular medicine·2026

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Communications medicine·2026

NEDD9 inhibits ox-LDL-induced endothelial anoikis to attenuate endothelial cell injury.

Cellular signalling·2026

Genome-wide transcriptomics and a machine learning-based random forest model identify novel biomarkers to predict phenotypic variability in Wilson disease.

Human immunology·2026

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Medicine·2026

Related Experiment Videos

Association between atopic asthma and a coding variant of Fc epsilon RI beta in a Japanese population

Related Concept Videos

A rare partnership: patient community and industry collaboration to shape the impact of real-world evidence on the rare disease ecosystem.

Immune and genetic aspects of asthma, allergy and parasitic worm infections: evolutionary links.

PTPRC (CD45) variation and disease association studied using single nucleotide polymorphism tagging.

The next extreme sport? Subdural haematoma in a patient with arachnoid cyst after head shaking competition.

Service provision of complex mutation analysis: a technical and economic appraisal using dystrophin point mutation analysis as an example.

Use of Gore-Tex tubing as a conduit for inferior alveolar and lingual nerve repair: experience with 6 cases.

Molecular basis of mucopolysaccharidosis IVA in a large cohort: genotype-phenotype correlations and reporting of 12 novel GALNS variants.

Shared genetic architecture of schizophrenia and lupus identifies pleiotropic loci with distinct downstream mechanisms.

Motor dysfunction phenotypes in a drosophila model validate DAO as an ALS gene.

Tissue-specific models of spinal muscular atrophy identify muscle functions required for Drosophila neuromuscular junction architecture.

Deep phenotyping of EHMT1 ankyrin repeat domain missense variants in Kleefstra syndrome by multi-tiered structural genomics analyses at atomic resolution.

MEF2C promoter variants in patent ductus arteriosus: a genetic and functional study.

Identification of Variants in Two Families With Congenital Cataract by Whole Exome Sequencing.

Golgi dysfunction in Alzheimer disease: from human multiomic signatures to therapeutic targets.

Current translational perspectives for diagnosis and individualized therapy in rare genetic diseases.

NEDD9 inhibits ox-LDL-induced endothelial anoikis to attenuate endothelial cell injury.

Genome-wide transcriptomics and a machine learning-based random forest model identify novel biomarkers to predict phenotypic variability in Wilson disease.

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Association between atopic asthma and a coding variant of Fc epsilon RI beta in a Japanese population

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