Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease (Q33377670)

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English	Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease	scientific article

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scholarly article

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26 July 2017

Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related disease (English)

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26 July 2017

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Valeria Bozzi

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Emanuele Panza

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Alessandro Pecci

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Alessandro Pecci

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Anna Savoia

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Paolo Gresele

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Marco Seri

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Catherine Klersy

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Catherine Klersy

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Pasi A. Koivisto

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Pasi A Koivisto

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Bianca Rocca

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Filomena Di Bari

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Filomena Di Bari

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Carlo L. Balduini

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Carlo L Balduini

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Patrizia Noris

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Carmine Pecoraro

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Carmine Pecoraro

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Achille Iolascon

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Achille Iolascon

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Núria Pujol-Moix

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Núria Pujol-Moix

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Paula G Heller

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Stefan Lethagen

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Fabrizio Fabris

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Carlo Dufour

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Antonio Granata

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Michael Doubek

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Patrizia Alvisi

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Dirk Schwabe

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Erica De Candia

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26 July 2017

Umberto Russo

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Ugo Ramenghi

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1 March 2008

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409-417

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Conditional expression of a truncated fragment of nonmuscle myosin II-A alters cell shape but not cytokinesis in HeLa cells

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https://api.crossref.org/works/10.1002%2FHUMU.20661

21 January 2018

Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome

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https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Genotype-phenotype correlation in MYH9-related thrombocytopenia

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https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Hereditary macrothrombocytopathia, nephritis and deafness

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https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Rod mutations associated with MYH9-related disorders disrupt nonmuscle myosin-IIA assembly

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https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Inherited thrombocytopenias: toward a molecular understanding of disorders of platelet production

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https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Sebastian platelet syndrome: a new variant of hereditary macrothrombocytopenia with leukocyte inclusions

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https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

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Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Atomic structure of scallop myosin subfragment S1 complexed with MgADP: a novel conformation of the myosin head

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https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Three conformational states of scallop myosin S1

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https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Mutations in human nonmuscle myosin IIA found in patients with May-Hegglin anomaly and Fechtner syndrome result in impaired enzymatic function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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A single class II myosin modulates T cell motility and stopping, but not synapse formation

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https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

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Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Identification of six novel MYH9 mutations and genotype-phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

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Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

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Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

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Inherited giant platelet disorders. Classification and literature review

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

inferred from DOI database lookup

Thrombocytopenia, giant platelets, and leukocyte inclusion bodies (May-Hegglin anomaly): clinical and laboratory findings.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a novel MYH9 mutation in a patient with May-Hegglin anomaly

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

inferred from DOI database lookup

Pathogenetic mechanisms of hematological abnormalities of patients with MYH9 mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

inferred from DOI database lookup

Towards a molecular understanding of cytokinesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

inferred from DOI database lookup

Fechtner syndrome: report of a third family and literature review

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

inferred from DOI database lookup

The MYH9 syndrome: report of a new case with a new mutation of the MYH9 gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

based on heuristic

inferred from DOI database lookup

Myosins: a diverse superfamily

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20661

7 January 2021

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Identifiers

10.1002/HUMU.20661

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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