(Q31127014)

English

Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

0 references

Giant platelet disorder

1 reference

based on heuristic

inferred from title

glomerulosclerosis

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

object named as

Masahito Ikawa

7

0 references

object named as

Masaru Okabe

8

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author name string

Nobuaki Suzuki

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Shinji Kunishima

2

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Makoto Ikejiri

3

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Shoichi Maruyama

4

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Michihiko Sone

5

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Akira Takagi

6

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Tetsuhito Kojima

9

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Hidehiko Saito

10

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Tomoki Naoe

11

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Tadashi Matsushita

12

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Europe PubMed Central

PMC publication ID

18 August 2017

language of work or name

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publication date

20 August 2013

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

8

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

e71187

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

copyright license

Creative Commons Attribution 4.0 International

20 August 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Heterozygous ITGA2B R995W mutation inducing constitutive activation of the αIIbβ3 receptor affects proplatelet formation and causes congenital macrothrombocytopenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Advances in the understanding of MYH9 disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Mac-1 (CD11b/CD18) links inflammation and thrombosis after glomerular injury

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Megakaryocyte-restricted MYH9 inactivation dramatically affects hemostasis while preserving platelet aggregation and secretion.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

The May-Hegglin anomaly gene MYH9 is a negative regulator of platelet biogenesis modulated by the Rho-ROCK pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

The immunoglobulin superfamily protein Izumo is required for sperm to fuse with eggs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Defects in cell adhesion and the visceral endoderm following ablation of nonmuscle myosin heavy chain II-A in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3748045

14 July 2018

A point mutation in the SH1 helix alters elasticity and thermal stability of myosin II.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0071187

21 January 2018

Proplatelet formation is regulated by the Rho/ROCK pathway

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0071187

21 January 2018

Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/23976996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New players in the pathogenesis of focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23976996

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0071187

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

2013PLoSO...871187S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

ResearchGate publication ID

0 references

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