Correlation between the clinical phenotype of MYH9-related disease and tissue distribution of class II nonmuscle myosin heavy chains (Q28592819)

Myosin, heavy polypeptide 9, non-muscle

GOA release 2020-03-11

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GOA release 2020-03-11

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Valeria Marigo

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Alessandro Pecci

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Alessandro Pecci

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Anna Savoia

object named as

Anna Savoia

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author name string

Alessandra Nigro

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31 January 2017

Donatella Montanaro

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31 January 2017

Mariateresa Di Stazio

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31 January 2017

Carlo L. Balduini

A millennial myosin census

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31 January 2017

1 June 2004

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31 January 2017

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31 January 2017

83

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31 January 2017

6

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31 January 2017

1125–1133

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31 January 2017

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Myosins: a diverse superfamily

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

A novel myosin heavy chain gene in human chromosome 19q13.3.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Induction of nonmuscle myosin heavy chain II-C by butyrate in RAW 264.7 mouse macrophages.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Chicken nonmuscle myosin heavy chains: differential expression of two mRNAs and evidence for two different polypeptides

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Stromal cell lines from mouse aorta-gonads-mesonephros subregions are potent supporters of hematopoietic stem cell activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Expression of the Runt domain-encoding PEBP2 alpha genes in T cells during thymic development

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Changes in expression of nonmuscle myosin heavy chain isoforms during muscle and nonmuscle tissue development

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Identification and characterization of nonmuscle myosin II-C, a new member of the myosin II family

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Cloning of the cDNA encoding rat myosin heavy chain-A and evidence for the absence of myosin heavy chain-B in cultured rat mast (RBL-2H3) cells.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Inhibition of the metastatic spread and growth of B16-BL6 murine melanoma by a synthetic matrix metalloproteinase inhibitor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Expression of non-muscle myosin isoforms in rabbit myometrium is estrogen-dependent

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012

Differential localization of cytoplasmic myosin II isoforms A and B in avian interphase and dividing embryonic and immortalized cardiomyocytes and other cell types in vitro.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.12.012