Normal neutrophil myosin IIA localization in an immunofluorescence analysis can rule out MYH9 disorders. (Q46246247)

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27 February 2020

title

Normal neutrophil myosin IIA localization in an immunofluorescence analysis can rule out MYH9 disorders (English)

1 reference

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immunofluorescence microscopy

27 February 2020

main subject

1 reference

2

1 reference

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27 February 2020

author name string

K Kitamura

1

1 reference

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27 February 2020

Y Shiraishi

3

1 reference

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27 February 2020

K Chiba

4

1 reference

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27 February 2020

H Tanaka

5

1 reference

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27 February 2020

K Furukawa

6

1 reference

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27 February 2020

S Miyano

7

1 reference

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27 February 2020

S Ogawa

8

1 reference

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27 February 2020

S Kunishima

9

1 reference

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27 February 2020

publication date

1 November 2013

1 reference

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Journal of Thrombosis and Haemostasis

27 February 2020

published in

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27 February 2020

volume

11

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27 February 2020

issue

11

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page(s)

2071-2073

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

27 February 2020

cites work

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

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

1 reference

ACTN1 mutations cause congenital macrothrombocytopenia

21 January 2018

1 reference

Frequent pathway mutations of splicing machinery in myelodysplasia

21 January 2018

1 reference

Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder.

21 January 2018

1 reference

Mutation of the beta1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/JTH.12406

1 reference

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27 February 2020

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