(Q33341898)

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Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes

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Europe PubMed Central

PubMed publication ID

25 July 2017

Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

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Vito Guarnieri

2

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Anna Savoia

5

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author name string

Maria D'Apolito

1

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Marianna Boncristiano

3

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Leopoldo Zelante

4

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

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publication date

1 March 2002

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Europe PubMed Central

PubMed publication ID

25 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

286

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Europe PubMed Central

PubMed publication ID

25 July 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

215-222

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital macrothrombocytopenia, leucocyte inclusions, deafness and proteinuria: functional and electron microscopic observations on platelets and megakaryocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Xenopus nonmuscle myosin heavy chain isoforms have different subcellular localizations and enzymatic activities

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

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/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Griscelli disease maps to chromosome 15q21 and is associated with mutations in the myosin-Va gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Myosins: a diverse superfamily

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Epstein syndrome: another renal disorder with mutations in the nonmuscle myosin heavy chain 9 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Differential expression and functions of cortical myosin IIA and IIB isotypes during meiotic maturation, fertilization, and mitosis in mouse oocytes and embryos

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Human nonmuscle myosin heavy chains are encoded by two genes located on different chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Nonmuscle myosin II-B is required for normal development of the mouse heart

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene dosage affects the cardiac and brain phenotype in nonmuscle myosin II-B-depleted mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900455-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0378-1119(02)00455-9

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

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