(Q37216184)

English

Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

scientific article published on 21 September 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Marie Lordkipanidzé

object named as

Marie Lordkipanidzé

3

0 references

Steve P. Watson

object named as

Steve P Watson

9

0 references

author name string

Ban B Dawood

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Gillian C Lowe

2

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Danai Bem

4

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Martina E Daly

5

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Mike Makris

6

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Andrew Mumford

7

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Jonathan T Wilde

8

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

language of work or name

0 references

publication date

21 September 2012

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

120

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

25

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

5041-5049

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

An intact PDZ motif is essential for correct P2Y12 purinoceptor traffic in human platelets.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Phenotypic approaches to gene mapping in platelet function disorders - identification of new variant of P2Y12, TxA2 and GPVI receptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

A novel thromboxane A2 receptor D304N variant that abrogates ligand binding in a patient with a bleeding diathesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

A compound heterozygous mutation in glycoprotein VI in a patient with a bleeding disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Diagnostic utility of light transmission platelet aggregometry: results from a prospective study of individuals referred for bleeding disorder assessments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Diagnostic approach to platelet function disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Congenital disorders associated with platelet dysfunctions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Congenital platelet disorders: overview of their mechanisms, diagnostic evaluation and treatment.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

A germline mutation in BLOC1S3/reduced pigmentation causes a novel variant of Hermansky-Pudlak syndrome (HPS8)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

A novel Syk-dependent mechanism of platelet activation by the C-type lectin receptor CLEC-2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Use of native or platelet count adjusted platelet rich plasma for platelet aggregation measurements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Inherited platelet-based bleeding disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Platelet-collagen interaction: is GPVI the central receptor?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Arg60 to Leu mutation of the human thromboxane A2 receptor in a dominantly inherited bleeding disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

6 September 2017

Rapid genetic diagnosis of heritable platelet function disorders with next-generation sequencing: proof-of-principle with Hermansky-Pudlak syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

3 September 2018

Guidelines for the laboratory investigation of heritable disorders of platelet function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

3 September 2018

Bleeding tendency and impaired platelet function in a patient carrying a heterozygous mutation in the thromboxane A2 receptor.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

3 September 2018

Src family kinases are essential for primary aggregation by G(i) -coupled receptors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

3 September 2018

Absence of collagen-induced platelet activation caused by compound heterozygous GPVI mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

3 September 2018

Results of a worldwide survey on the assessment of platelet function by light transmission aggregometry: a report from the platelet physiology subcommittee of the SSC of the ISTH.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

3 September 2018

Standardization of light transmittance aggregometry for monitoring antiplatelet therapy: an adjustment for platelet count is not necessary

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

3 September 2018

Reference curves for aggregation and ATP secretion to aid diagnose of platelet-based bleeding disorders: effect of inhibition of ADP and thromboxane A(2) pathways.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3790949

3 September 2018

Mutations of the platelet thromboxane A2 (TXA2) receptor in patients characterized by the absence of TXA2-induced platelet aggregation despite normal TXA2 binding activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/23002116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited defects in platelet signaling mechanisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/23002116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathogenetic analysis of five cases with a platelet disorder characterized by the absence of thromboxane A2 (TXA2)-induced platelet aggregation in spite of normal TXA2 binding activity

1 reference

https://pubmed.ncbi.nlm.nih.gov/23002116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited platelet abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/23002116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Platelet aggregation studies: autologous platelet-poor plasma inhibits platelet aggregation when added to platelet-rich plasma to normalize platelet count

1 reference

https://pubmed.ncbi.nlm.nih.gov/23002116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1182/BLOOD-2012-07-444281

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

release_2o3w7gpguzce3g5i2m7t2wkxjm

1 reference

https://api.fatcat.wiki/v0/release/2o3w7gpguzce3g5i2m7t2wkxjm

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

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