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Article

Successful immunostaining demonstrates abnormal intracytoplasmic MYH9 protein (NMMHC-IIA) in neutrophils of a dog with May-Hegglin anomaly.

Veterinary clinical pathology - 1 Dec 2011

Flatland Bente, Kunishima Shinji

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22136472
DOI: 10.1111/j.1939-165X.2011.00378.x

Genes

MYH9

Provenance

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Successful immunostaining demonstrates abnormal intracytoplasmic MYH9 protein (NMMHC-IIA) in neutrophils of a dog with May-Hegglin anomaly.PMID 22136472Read ↗

[May-Hegglin anomaly: past and present--novel diagnostic test and new concept of the disease].Semantic proximity Read ↗

Clinical, pathological, and genetic analysis of ten patients with MYH9-related disease.Semantic proximity Read ↗

[Clinical and molecular-biological study of a May-Hegglin anomaly family].Semantic proximity Read ↗

[A non-familial May-Hegglin anomaly accompanying with MYH9 gene R1933X mutation and I1626V polymorphism].Semantic proximity Read ↗

Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations.Semantic proximity Read ↗

R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura.Semantic proximity Read ↗

Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders.Semantic proximity Read ↗

Left shift and toxic change in heterophils and neutrophils of non‐mammalian vertebrates: A comparative review, image atlas, and practical considerationsSemantic proximity Read ↗

Multiorgan neutrophilic inflammation in a Border Collie with "trapped" neutrophil syndrome.Semantic proximity Read ↗

A notable case report of May-Hegglin anomaly with immune complex-related nephropathy: a genetic and histological analysis.Semantic proximity Read ↗

Clinical manifestation and molecular genetic characterization of MYH9 disorders.Semantic proximity Read ↗

A Trp33Arg mutation at exon 1 of the MYH9 gene in a Korean patient with May-Hegglin anomaly.Semantic proximity Read ↗

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