(Q37146072)

18 August 2017

Haploinsufficiency of the platelet P2Y12 gene in a family with congenital bleeding diathesis (English)

1 reference

18 August 2017

0 references

0 references

Gessica Fontana

1

1 reference

18 August 2017

Jerry Ware

series ordinal

2

1 reference

18 August 2017

Marco Cattaneo

series ordinal

3

1 reference

18 August 2017

19 February 2009

1 reference

18 August 2017

1 reference

18 August 2017

94

1 reference

18 August 2017

4

1 reference

18 August 2017

581-584

1 reference

Molecular bases of defective signal transduction in the platelet P2Y12 receptor of a patient with congenital bleeding

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663622

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663622

Identification of the platelet ADP receptor targeted by antithrombotic drugs

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663622

An inherited bleeding disorder linked to a defective interaction between ADP and its receptor on platelets. Its influence on glycoprotein IIb-IIIa complex function

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663622

Impaired platelet function in a patient with P2Y12 deficiency caused by a mutation in the translation initiation codon

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663622

Identification of a new congenital defect of platelet function characterized by severe impairment of platelet responses to adenosine diphosphate

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663622

Rapid detection of VHL exon deletions using real-time quantitative PCR.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663622

Platelets from a patient heterozygous for the defect of P2CYC receptors for ADP have a secretion defect despite normal thromboxane A2 production and normal granule stores: further evidence that some cases of platelet 'primary secretion defect' are h

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2663622

3 September 2018

Identifiers

DOI

10.3324/HAEMATOL.13611

1 reference

release_jmwkroqmwjgbhfqjkhdyyakg7e

18 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jmwkroqmwjgbhfqjkhdyyakg7e

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

18 August 2017

PubMed publication ID

19229056

1 reference