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Article

Quantitative Western blot analysis of plasma ADAMTS13 antigen in patients with Upshaw-Schulman syndrome.

Thrombosis research - 1 Jan 2007

Ishizashi Hiromichi, Yagi Hideo, Matsumoto Masanori, Soejima Kenji, Nakagaki Tomohiro, Fujimura Yoshihiro

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Share to ADAM Proteins
Share to ADAMTS13 Protein
Share to Blotting, Western
Share to Chromosomes, Human, Pair 9

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Enzyme-Linked Immunosorbent Assay

Share to Genes, Recessive

Share to Genetic Carrier Screening

Share to Purpura, Thrombotic Thrombocytopenic

Source

Identifiers

PMID: 17030346
DOI: 10.1016/j.thromres.2006.07.012

Genes

ADAMTS13

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

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Quantitative Western blot analysis of plasma ADAMTS13 antigen in patients with Upshaw-Schulman syndrome.PMID 17030346Read ↗

Polymorphisms and mutations of ADAMTS13 in the Japanese population and estimation of the number of patients with Upshaw–Schulman syndromeSemantic proximity Read ↗

ADAMTS-13 activity in von Willebrand disease.Semantic proximity Read ↗

Inherited and de novo mutations of ADAMTS13 in a patient with Upshaw-Schulman syndrome.Semantic proximity Read ↗

Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw-Schulman Syndrome Investigated in Germany.Semantic proximity Read ↗

A novel mutation in ADAMTS13 of a child with Upshaw-Schulman Syndrome.Semantic proximity Read ↗

The homozygous p.C1024R- ADAMTS13 gene mutation links to a late-onset phenotype of Upshaw-Schulman syndrome in Japan.Semantic proximity Read ↗

Natural history of Upshaw-Schulman syndrome based on ADAMTS13 gene analysis in Japan.Semantic proximity Read ↗

Inherited ADAMTS13 deficiency (Upshaw-Schulman syndrome): a short review.Semantic proximity Read ↗

ADAMTS13 Gene Mutations Influence ADAMTS13 Conformation and Disease Age-Onset in the French Cohort of Upshaw–Schulman SyndromeSemantic proximity Read ↗

Mutation Spectrum of ADAMTS13 Gene in Patients with Upshaw-Schulman Syndrome (USS) in Russia.Semantic proximity Read ↗

GWA study for ADAMTS13 activity.Semantic proximity Read ↗

Novel ADAMTS13 mutations in an obstetric patient with Upshaw-Schulman syndrome.Semantic proximity Read ↗

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