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

26 July 2017

title

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

1 reference

26 July 2017

Valeria Bozzi

0 references

Emanuele Panza

0 references

Alessandro Pecci

0 references

Anna Savoia

0 references

Paolo Gresele

0 references

Marco Seri

0 references

Catherine Klersy

0 references

Pasi A Koivisto

1 reference

26 July 2017

Bianca Rocca

1 reference

26 July 2017

Filomena Di Bari

1 reference

26 July 2017

Carlo L Balduini

1 reference

26 July 2017

Patrizia Noris

1 reference

26 July 2017

Carmine Pecoraro

1 reference

26 July 2017

Achille Iolascon

1 reference

26 July 2017

Núria Pujol-Moix

1 reference

26 July 2017

Paula G Heller

1 reference

26 July 2017

Stefan Lethagen

1 reference

26 July 2017

Fabrizio Fabris

1 reference

26 July 2017

Carlo Dufour

1 reference

26 July 2017

Antonio Granata

1 reference

26 July 2017

Michael Doubek

1 reference

26 July 2017

Patrizia Alvisi

1 reference

26 July 2017

Dirk Schwabe

1 reference

26 July 2017

Erica De Candia

1 reference

26 July 2017

Umberto Russo

1 reference

26 July 2017

Ugo Ramenghi

1 reference

26 July 2017

language of work or name

1 reference

1 March 2008

1 reference

26 July 2017

1 reference

26 July 2017

1 reference

26 July 2017

1 reference

26 July 2017

page(s)

409-417

1 reference

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

26 July 2017

cites work

1 reference

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

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

21 January 2018

1 reference

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

7 January 2021

Genotype-phenotype correlation in MYH9-related thrombocytopenia

1 reference

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

7 January 2021

Hereditary macrothrombocytopathia, nephritis and deafness

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

1 reference

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

7 January 2021

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

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

1 reference

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

7 January 2021

Three conformational states of scallop myosin S1

1 reference

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

7 January 2021

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

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

1 reference

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

7 January 2021

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

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

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

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

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

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

Inherited giant platelet disorders. Classification and literature review

1 reference

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

7 January 2021

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

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

Pathogenetic mechanisms of hematological abnormalities of patients with MYH9 mutations

1 reference

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

7 January 2021

Towards a molecular understanding of cytokinesis

1 reference

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

7 January 2021

Fechtner syndrome: report of a third family and literature review

1 reference

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

7 January 2021

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

Myosins: a diverse superfamily

1 reference

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

7 January 2021

Identifiers

DOI

10.1002/HUMU.20661

1 reference

26 July 2017

1 reference