PEAR1 polymorphisms as a prognostic factor in hemostasis and cardiovascular diseases

Platelet Endothelial Aggregation Receptor (PEAR1), as a platelet receptor, plays a vital role in hemostasis. This receptor, by its extracellular part, causes platelet adhesion and consequently initiates platelet aggregation. Dysfunction of PEAR1 can disrupt platelet aggregation in patients with card...

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Published inJournal of thrombosis and thrombolysis Vol. 51; no. 1; pp. 89 - 95
Main Authors Ansari, Narges, Najafi, Sahar, Shahrabi, Saied, Saki, Najmaldin
Format Journal Article
LanguageEnglish
Published New York Springer US 01.01.2021
Springer Nature B.V
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ISSN0929-5305
1573-742X
1573-742X
DOI10.1007/s11239-020-02149-w

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Abstract Platelet Endothelial Aggregation Receptor (PEAR1), as a platelet receptor, plays a vital role in hemostasis. This receptor, by its extracellular part, causes platelet adhesion and consequently initiates platelet aggregation. Dysfunction of PEAR1 can disrupt platelet aggregation in patients with cardiovascular diseases (CVDs). The content used in this paper has been taken from English language articles (2005–2020) retrieved from Pubmed database and Google scholar search engine using “Cardiovascular Disease”, “PEAR1”, “Polymorphism”, and “Platelet Aggregation” keywords. Some PEAR1 polymorphisms can disrupt homeostasis and interfere with the function mechanism of cardiac drugs. Since polymorphisms in this gene affect platelet function and the platelet aggregation process, PEAR1 could be further studied in the future as an essential factor in controlling the treatment process of patients with cardiovascular diseases. PEAR1 polymorphisms through disruption of the platelet aggregation process can be a risk factor in patients with CVDs. Therefore, controlling patients through genetic testing and the evaluation of PEAR1 polymorphisms can help improve the treatment process of patients. According to the studies on the PEAR1 gene and the effect of different polymorphisms on some crucial issues in CVDs patients (changes in platelet activity), it is clear that if there is a significant relationship between polymorphisms and CVDs, they can be used as prognostic and diagnostic markers. This study aims to evaluate the prognosis and drug treatment of the PEAR1 gene in CVDs patients.
AbstractList Platelet Endothelial Aggregation Receptor (PEAR1), as a platelet receptor, plays a vital role in hemostasis. This receptor, by its extracellular part, causes platelet adhesion and consequently initiates platelet aggregation. Dysfunction of PEAR1 can disrupt platelet aggregation in patients with cardiovascular diseases (CVDs). The content used in this paper has been taken from English language articles (2005–2020) retrieved from Pubmed database and Google scholar search engine using “Cardiovascular Disease”, “PEAR1”, “Polymorphism”, and “Platelet Aggregation” keywords. Some PEAR1 polymorphisms can disrupt homeostasis and interfere with the function mechanism of cardiac drugs. Since polymorphisms in this gene affect platelet function and the platelet aggregation process, PEAR1 could be further studied in the future as an essential factor in controlling the treatment process of patients with cardiovascular diseases. PEAR1 polymorphisms through disruption of the platelet aggregation process can be a risk factor in patients with CVDs. Therefore, controlling patients through genetic testing and the evaluation of PEAR1 polymorphisms can help improve the treatment process of patients. According to the studies on the PEAR1 gene and the effect of different polymorphisms on some crucial issues in CVDs patients (changes in platelet activity), it is clear that if there is a significant relationship between polymorphisms and CVDs, they can be used as prognostic and diagnostic markers. This study aims to evaluate the prognosis and drug treatment of the PEAR1 gene in CVDs patients.
Platelet Endothelial Aggregation Receptor (PEAR1), as a platelet receptor, plays a vital role in hemostasis. This receptor, by its extracellular part, causes platelet adhesion and consequently initiates platelet aggregation. Dysfunction of PEAR1 can disrupt platelet aggregation in patients with cardiovascular diseases (CVDs). The content used in this paper has been taken from English language articles (2005-2020) retrieved from Pubmed database and Google scholar search engine using "Cardiovascular Disease", "PEAR1", "Polymorphism", and "Platelet Aggregation" keywords. Some PEAR1 polymorphisms can disrupt homeostasis and interfere with the function mechanism of cardiac drugs. Since polymorphisms in this gene affect platelet function and the platelet aggregation process, PEAR1 could be further studied in the future as an essential factor in controlling the treatment process of patients with cardiovascular diseases. PEAR1 polymorphisms through disruption of the platelet aggregation process can be a risk factor in patients with CVDs. Therefore, controlling patients through genetic testing and the evaluation of PEAR1 polymorphisms can help improve the treatment process of patients. According to the studies on the PEAR1 gene and the effect of different polymorphisms on some crucial issues in CVDs patients (changes in platelet activity), it is clear that if there is a significant relationship between polymorphisms and CVDs, they can be used as prognostic and diagnostic markers. This study aims to evaluate the prognosis and drug treatment of the PEAR1 gene in CVDs patients.Platelet Endothelial Aggregation Receptor (PEAR1), as a platelet receptor, plays a vital role in hemostasis. This receptor, by its extracellular part, causes platelet adhesion and consequently initiates platelet aggregation. Dysfunction of PEAR1 can disrupt platelet aggregation in patients with cardiovascular diseases (CVDs). The content used in this paper has been taken from English language articles (2005-2020) retrieved from Pubmed database and Google scholar search engine using "Cardiovascular Disease", "PEAR1", "Polymorphism", and "Platelet Aggregation" keywords. Some PEAR1 polymorphisms can disrupt homeostasis and interfere with the function mechanism of cardiac drugs. Since polymorphisms in this gene affect platelet function and the platelet aggregation process, PEAR1 could be further studied in the future as an essential factor in controlling the treatment process of patients with cardiovascular diseases. PEAR1 polymorphisms through disruption of the platelet aggregation process can be a risk factor in patients with CVDs. Therefore, controlling patients through genetic testing and the evaluation of PEAR1 polymorphisms can help improve the treatment process of patients. According to the studies on the PEAR1 gene and the effect of different polymorphisms on some crucial issues in CVDs patients (changes in platelet activity), it is clear that if there is a significant relationship between polymorphisms and CVDs, they can be used as prognostic and diagnostic markers. This study aims to evaluate the prognosis and drug treatment of the PEAR1 gene in CVDs patients.
Author Saki, Najmaldin
Ansari, Narges
Najafi, Sahar
Shahrabi, Saied
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Cites_doi 10.1074/mcp.M114.046946
10.1016/j.bcmd.2005.12.026
10.3390/ijms19041069
10.1371/journal.pone.0111816
10.1042/bj20150192
10.3389/fphar.2018.00490
10.1016/j.jacc.2011.12.062
10.1182/blood-2010-11-320788
10.1182/blood-2009-02-202614
10.1016/j.thromres.2018.01.026
10.1182/blood-2015-11-682153
10.1182/bloodadvances.2018024950
10.1080/09537104.2018.1447659
10.1161/atvbaha.108.168971
10.1161/circulationaha.106.667584
10.1074/jbc.M413411200
10.1182/blood-2016-06-723940
10.1160/th12-09-0645
10.1515/hmbci-2013-0055
10.1038/aps.2016.90
10.1182/blood-2012-10-462887
10.3109/09537104.2015.1111321
10.1016/j.jns.2018.03.013
10.1080/00498254.2016.1271962
10.1097/md.0000000000005687
10.1016/j.thromres.2016.08.026
10.1159/000488101
10.1111/ahg.12285
10.2217/pgs.13.108
10.1016/j.amjcard.2006.04.015
10.1038/nrcardio.2017.108
10.1371/journal.pone.0064179
10.1016/j.thromres.2016.02.031
10.5551/jat.39982
10.1097/crd.0000000000000181
10.1186/s12881-017-0411-x
10.3109/08037051.2014.986928
10.1371/journal.pone.0138795
10.1038/ng.604
10.1080/10428194.2019.1630622
10.1007/s12094-019-02132-9
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Keywords Platelet aggregation
Cardiovascular diseases
PEAR1
Hemostasis
Polymorphism
Language English
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PublicationSubtitle A Journal for Translation, Application and Therapeutics in Thrombosis and Vascular Science
PublicationTitle Journal of thrombosis and thrombolysis
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References Kardeby, Falker, Haining (CR26) 2019; 3
Izzi, Pistoni, Cludts (CR45) 2016; 128
Xiang, Cui, Zhao (CR40) 2013; 14
Faraday, Yanek, Yang (CR7) 2011; 118
Faraday, Becker, Yanek (CR30) 2006; 98
Peng, Zhao, Zhou (CR46) 2016; 37
Nie, Li, Qin (CR39) 2018; 163
Kim, Suktitipat, Yanek (CR4) 2013; 8
Elwood, Renaud, Sharp (CR20) 1991; 83
Getz, Manne, Buitrago (CR24) 2013; 109
Roberts, Stewart (CR43) 2012; 60
Farré, Modrego, Zamorano-León (CR3) 2014; 18
Kauskot, Vandenbriele, Louwette (CR14) 2013; 121
Yao, Tang, Zhang (CR21) 2016; 141
Mozaffarian, Benjamin (CR2) 2016; 133
Fisch, Yerges-Armstrong, Backman (CR44) 2015; 10
Li, Hu, Wen (CR8) 2017; 47
Vandenbriele, Sun, Criel (CR15) 2016; 27
Stimpfle, Bauer, Rath (CR41) 2018; 9
Jones, Bray, Garner (CR19) 2009; 114
CR6
Sun, Vandenbriele, Kauskot (CR12) 2015; 14
Criel, Izzi, Vandenbriele (CR13) 2016; 146
Wurtz, Nissen, Grove (CR32) 2014; 9
Kardeby, Fälker, Haining (CR17) 2019; 3
CR28
Kauskot, Di Michele, Loyen (CR5) 2012; 119
Yao, Tang, He (CR22) 2018; 25
Nanda, Bao, Lin (CR10) 2005; 280
Lewis, Ryan, O’connell (CR36) 2013; 6
Xu, Liu, Ott (CR29) 2018; 388
Nawarskas, Montoya (CR34) 2018; 26
Olivi, Vandenbriele, Gu (CR42) 2015; 24
Fu, Sun, Liang (CR47) 2016; 95
Lavie, Arena, Alpert (CR1) 2018; 15
Izzi, Noro, Cludts (CR37) 2018; 19
Xu, Ye, Zhang (CR9) 2019; 12
Herrera-Galeano, Becker, Wilson (CR31) 2008; 28
Johnson (CR38) 2016; 128
Pi, Xu, Fu (CR11) 2019; 83
Zhang, Zhu, Li (CR33) 2018; 140
Shahrabi, Behzad, Jaseb (CR27) 1976; 2018
Keramati, Yanek, Iyer (CR23) 2018; 19
Faraday, Yanek, Mathias (CR35) 2007; 115
Johnson, Yanek, Chen (CR48) 2010; 42
Nanda, Phillips (CR16) 2006; 36
Yang, Petit, Cauwenberghs (CR18) 2017; 18
Alshehri, Montague, Watson (CR25) 2015; 468
D Mozaffarian (2149_CR2) 2016; 133
N Nanda (2149_CR16) 2006; 36
TM Getz (2149_CR24) 2013; 109
AD Johnson (2149_CR48) 2010; 42
M Wurtz (2149_CR32) 2014; 9
2149_CR28
AR Keramati (2149_CR23) 2018; 19
Y Yao (2149_CR21) 2016; 141
L Pi (2149_CR11) 2019; 83
JE Herrera-Galeano (2149_CR31) 2008; 28
N Nanda (2149_CR10) 2005; 280
B Izzi (2149_CR37) 2018; 19
R Roberts (2149_CR43) 2012; 60
Y Yao (2149_CR22) 2018; 25
CJ Lavie (2149_CR1) 2018; 15
N Faraday (2149_CR35) 2007; 115
AS Fisch (2149_CR44) 2015; 10
CI Jones (2149_CR19) 2009; 114
F Stimpfle (2149_CR41) 2018; 9
B Izzi (2149_CR45) 2016; 128
Y Fu (2149_CR47) 2016; 95
LL Peng (2149_CR46) 2016; 37
A Kauskot (2149_CR5) 2012; 119
S Shahrabi (2149_CR27) 1976; 2018
S Zhang (2149_CR33) 2018; 140
OM Alshehri (2149_CR25) 2015; 468
A Kauskot (2149_CR14) 2013; 121
AL Farré (2149_CR3) 2014; 18
Y Kim (2149_CR4) 2013; 8
M Li (2149_CR8) 2017; 47
C Vandenbriele (2149_CR15) 2016; 27
JJ Nawarskas (2149_CR34) 2018; 26
L Olivi (2149_CR42) 2015; 24
JP Lewis (2149_CR36) 2013; 6
XY Nie (2149_CR39) 2018; 163
K Xu (2149_CR9) 2019; 12
AD Johnson (2149_CR38) 2016; 128
PC Elwood (2149_CR20) 1991; 83
N Faraday (2149_CR7) 2011; 118
C Kardeby (2149_CR26) 2019; 3
N Faraday (2149_CR30) 2006; 98
Y Sun (2149_CR12) 2015; 14
M Criel (2149_CR13) 2016; 146
Q Xiang (2149_CR40) 2013; 14
WY Yang (2149_CR18) 2017; 18
2149_CR6
C Kardeby (2149_CR17) 2019; 3
K Xu (2149_CR29) 2018; 388
References_xml – volume: 14
  start-page: 1265
  issue: 5
  year: 2015
  end-page: 1274
  ident: CR12
  article-title: A human platelet receptor protein microarray identifies the high affinity immunoglobulin E receptor subunit alpha (FcepsilonR1alpha) as an Activating Platelet Endothelium Aggregation Receptor 1 (PEAR1) ligand
  publication-title: Mol Cell Proteomics
  doi: 10.1074/mcp.M114.046946
– volume: 36
  start-page: 228
  issue: 2
  year: 2006
  end-page: 231
  ident: CR16
  article-title: Novel targets for antithrombotic drug discovery
  publication-title: Blood Cells Mol Dis
  doi: 10.1016/j.bcmd.2005.12.026
– volume: 2018
  start-page: 11976
  year: 1976
  end-page: 11981
  ident: CR27
  article-title: Thrombocytopenia in leukemia: pathogenesis and prognosis
  publication-title: Histol Histopathol
– volume: 6
  start-page: 184
  issue: 2
  year: 2013
  end-page: 192
  ident: CR36
  article-title: Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes clinical perspective
  publication-title: Circulation
– volume: 12
  start-page: e007019
  issue: 5
  year: 2019
  ident: CR9
  article-title: Impact of platelet endothelial aggregation receptor-1 genotypes on platelet reactivity and early cardiovascular outcomes in patients undergoing percutaneous coronary intervention and treated with aspirin and clopidogrel
  publication-title: Circulation
– volume: 19
  start-page: 1069
  issue: 4
  year: 2018
  ident: CR37
  article-title: Cell-specific PEAR1 methylation studies reveal a locus that coordinates expression of multiple genes
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms19041069
– volume: 9
  start-page: e111816
  issue: 10
  year: 2014
  ident: CR32
  article-title: Genetic determinants of on-aspirin platelet reactivity: focus on the influence of PEAR1
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0111816
– volume: 468
  start-page: 459
  issue: 3
  year: 2015
  end-page: 473
  ident: CR25
  article-title: Activation of glycoprotein VI (GPVI) and C-type lectin-like receptor-2 (CLEC-2) underlies platelet activation by diesel exhaust particles and other charged/hydrophobic ligands
  publication-title: Biochem J
  doi: 10.1042/bj20150192
– volume: 133
  start-page: e38
  issue: 4
  year: 2016
  ident: CR2
  article-title: Heart disease and stroke statistics-2016 update: a report from the American Heart Association
  publication-title: Circulation
– volume: 9
  start-page: 490
  year: 2018
  ident: CR41
  article-title: Variants of PEAR1 are associated with outcome in patients with ACS and stable CAD undergoing PCI
  publication-title: Front Pharmacol
  doi: 10.3389/fphar.2018.00490
– volume: 60
  start-page: 1715
  issue: 18
  year: 2012
  end-page: 1721
  ident: CR43
  article-title: Genes and coronary artery disease: where are we?
  publication-title: Am Coll Cardiol
  doi: 10.1016/j.jacc.2011.12.062
– volume: 118
  start-page: 3367
  issue: 12
  year: 2011
  end-page: 3375
  ident: CR7
  article-title: Identification of a specific intronic PEAR1 gene variant associated with greater platelet aggregability and protein expression
  publication-title: Blood
  doi: 10.1182/blood-2010-11-320788
– volume: 114
  start-page: 1405
  issue: 7
  year: 2009
  end-page: 1416
  ident: CR19
  article-title: A functional genomics approach reveals novel quantitative trait loci associated with platelet signaling pathways
  publication-title: Blood
  doi: 10.1182/blood-2009-02-202614
– ident: CR6
– volume: 163
  start-page: 77
  year: 2018
  end-page: 82
  ident: CR39
  article-title: Genetic mutations in PEAR1 associated with cardiovascular outcomes in Chinese patients with acute coronary syndrome
  publication-title: Thromb Res
  doi: 10.1016/j.thromres.2018.01.026
– volume: 128
  start-page: 1003
  issue: 7
  year: 2016
  end-page: 1012
  ident: CR45
  article-title: Allele-specific DNA methylation reinforces PEAR1 enhancer activity
  publication-title: Blood
  doi: 10.1182/blood-2015-11-682153
– volume: 3
  start-page: 275
  issue: 3
  year: 2019
  end-page: 287
  ident: CR26
  article-title: Synthetic glycopolymers and natural fucoidans cause human platelet aggregation via PEAR1 and GPIbalpha
  publication-title: Blood Adv
  doi: 10.1182/bloodadvances.2018024950
– volume: 83
  start-page: 38
  issue: 1
  year: 1991
  end-page: 44
  ident: CR20
  article-title: Ischemic heart disease and platelet aggregation
  publication-title: Caerphilly Collab Heart Dis Stud
– volume: 19
  start-page: 1
  year: 2018
  end-page: 7
  ident: CR23
  article-title: Targeted deep sequencing of the PEAR1 locus for platelet aggregation in European and African American families
  publication-title: Platelets
  doi: 10.1080/09537104.2018.1447659
– volume: 28
  start-page: 1484
  issue: 8
  year: 2008
  end-page: 1490
  ident: CR31
  article-title: A novel variant in the platelet endothelial aggregation receptor-1 gene is associated with increased platelet aggregability
  publication-title: Arterioscl Thrombo Vasc Biol
  doi: 10.1161/atvbaha.108.168971
– volume: 115
  start-page: 2490
  issue: 19
  year: 2007
  end-page: 2496
  ident: CR35
  article-title: Heritability of platelet responsiveness to aspirin in activation pathways directly and indirectly related to cyclooxygenase-1
  publication-title: Circulation
  doi: 10.1161/circulationaha.106.667584
– volume: 280
  start-page: 24680
  issue: 26
  year: 2005
  end-page: 24689
  ident: CR10
  article-title: Platelet endothelial aggregation receptor 1 (PEAR1), a novel epidermal growth factor repeat-containing transmembrane receptor, participates in platelet contact-induced activation
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M413411200
– volume: 128
  start-page: 890
  issue: 7
  year: 2016
  end-page: 892
  ident: CR38
  article-title: Pairing megakaryopoiesis methylation with PEAR1
  publication-title: Blood
  doi: 10.1182/blood-2016-06-723940
– volume: 109
  start-page: 1131
  issue: 6
  year: 2013
  end-page: 1140
  ident: CR24
  article-title: Dextran sulphate induces fibrinogen receptor activation through a novel Syk-independent PI-3 kinase-mediated tyrosine kinase pathway in platelets
  publication-title: Thromb Haemost
  doi: 10.1160/th12-09-0645
– volume: 18
  start-page: 27
  issue: 1
  year: 2014
  end-page: 36
  ident: CR3
  article-title: Effects of hormones on platelet aggregation
  publication-title: Hormone Mol Biol Clin Investig
  doi: 10.1515/hmbci-2013-0055
– volume: 37
  start-page: 1442
  issue: 11
  year: 2016
  end-page: 1448
  ident: CR46
  article-title: Associations of MDR1, TBXA2R, PLA2G7, and PEAR1 genetic polymorphisms with the platelet activity in Chinese ischemic stroke patients receiving aspirin therapy
  publication-title: Acta Pharmacol Sin
  doi: 10.1038/aps.2016.90
– volume: 121
  start-page: 5208
  issue: 26
  year: 2013
  end-page: 5217
  ident: CR14
  article-title: PEAR1 attenuates megakaryopoiesis via control of the PI3K/PTEN pathway
  publication-title: Blood
  doi: 10.1182/blood-2012-10-462887
– volume: 27
  start-page: 365
  issue: 4
  year: 2016
  end-page: 372
  ident: CR15
  article-title: Dextran sulfate triggers platelet aggregation via direct activation of PEAR1
  publication-title: Platelets
  doi: 10.3109/09537104.2015.1111321
– volume: 388
  start-page: 141
  year: 2018
  end-page: 145
  ident: CR29
  article-title: The combined effects of cardiovascular disease related SNPs on ischemic stroke
  publication-title: J Neurol Sci
  doi: 10.1016/j.jns.2018.03.013
– volume: 47
  start-page: 1130
  issue: 12
  year: 2017
  end-page: 1138
  ident: CR8
  article-title: Association of PEAR1 rs12041331 polymorphism and pharmacodynamics of ticagrelor in healthy Chinese volunteers
  publication-title: Xenobiotica
  doi: 10.1080/00498254.2016.1271962
– volume: 95
  start-page: e5687
  issue: 51
  year: 2016
  ident: CR47
  article-title: PEAR1 gene polymorphism in a Chinese pedigree with pulmonary thromboembolism
  publication-title: Medicine
  doi: 10.1097/md.0000000000005687
– volume: 146
  start-page: 76
  year: 2016
  end-page: 83
  ident: CR13
  article-title: Absence of Pear1 does not affect murine platelet function in vivo
  publication-title: Thrombosis Res
  doi: 10.1016/j.thromres.2016.08.026
– volume: 140
  start-page: 21
  issue: 1
  year: 2018
  end-page: 29
  ident: CR33
  article-title: Study of the association of PEAR1, P2Y12, and UGT2A1 polymorphisms with platelet reactivity in response to dual antiplatelet therapy in Chinese patients
  publication-title: Cardiology
  doi: 10.1159/000488101
– volume: 83
  start-page: 54
  issue: 1
  year: 2019
  end-page: 62
  ident: CR11
  article-title: A PEAR1 polymorphism (rs12041331) is associated with risk of coronary artery aneurysm in Kawasaki disease
  publication-title: Ann Hum Genet
  doi: 10.1111/ahg.12285
– volume: 14
  start-page: 1179
  issue: 10
  year: 2013
  end-page: 1189
  ident: CR40
  article-title: Identification of PEAR1 SNPs and their influences on the variation in prasugrel pharmacodynamics
  publication-title: Pharmacogenomics
  doi: 10.2217/pgs.13.108
– volume: 98
  start-page: 774
  issue: 6
  year: 2006
  end-page: 779
  ident: CR30
  article-title: Relation between atherosclerosis risk factors and aspirin resistance in a primary prevention population
  publication-title: Am J Cardiol
  doi: 10.1016/j.amjcard.2006.04.015
– volume: 15
  start-page: 45
  issue: 1
  year: 2018
  ident: CR1
  article-title: Management of cardiovascular diseases in patients with obesity
  publication-title: Nat Rev Cardiol
  doi: 10.1038/nrcardio.2017.108
– volume: 8
  start-page: e64179
  issue: 5
  year: 2013
  ident: CR4
  article-title: Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0064179
– volume: 141
  start-page: 28
  year: 2016
  end-page: 34
  ident: CR21
  article-title: Association of PEAR1 genetic variants with platelet reactivity in response to dual antiplatelet therapy with aspirin and clopidogrel in the Chinese patient population after percutaneous coronary intervention
  publication-title: Thromb Res
  doi: 10.1016/j.thromres.2016.02.031
– volume: 119
  start-page: 4056
  issue: 17
  year: 2012
  end-page: 4065
  ident: CR5
  article-title: A novel mechanism of sustained platelet αIIbβ3 activation via PEAR1
  publication-title: Blood J Am Soc Hematol
– volume: 25
  start-page: 454
  issue: 5
  year: 2018
  end-page: 459
  ident: CR22
  article-title: Effect of PEAR1 genetic variants on 1-year outcomes in chinese patients with acute myocardial infarction after percutaneous coronary intervention
  publication-title: J Atheroscler Thromb
  doi: 10.5551/jat.39982
– volume: 26
  start-page: 107
  issue: 2
  year: 2018
  end-page: 111
  ident: CR34
  article-title: Switching from ticagrelor or prasugrel to clopidogrel
  publication-title: Cardiol Rev
  doi: 10.1097/crd.0000000000000181
– volume: 18
  start-page: 45
  issue: 1
  year: 2017
  ident: CR18
  article-title: PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population
  publication-title: BMC Med Genet
  doi: 10.1186/s12881-017-0411-x
– ident: CR28
– volume: 24
  start-page: 61
  issue: 1
  year: 2015
  end-page: 64
  ident: CR42
  article-title: PEAR1 is not a human hypertension-susceptibility gene
  publication-title: Blodd Press
  doi: 10.3109/08037051.2014.986928
– volume: 3
  start-page: 275
  issue: 3
  year: 2019
  end-page: 287
  ident: CR17
  article-title: Synthetic glycopolymers and natural fucoidans cause human platelet aggregation via PEAR1 and GPIbα
  publication-title: Blood Adv
  doi: 10.1182/bloodadvances.2018024950
– volume: 10
  start-page: e0138795
  issue: 9
  year: 2015
  ident: CR44
  article-title: Genetic variation in the platelet endothelial aggregation receptor 1 gene results in endothelial dysfunction
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0138795
– volume: 42
  start-page: 608
  issue: 7
  year: 2010
  ident: CR48
  article-title: Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists
  publication-title: Nat Genet
  doi: 10.1038/ng.604
– volume: 25
  start-page: 454
  issue: 5
  year: 2018
  ident: 2149_CR22
  publication-title: J Atheroscler Thromb
  doi: 10.5551/jat.39982
– volume: 128
  start-page: 890
  issue: 7
  year: 2016
  ident: 2149_CR38
  publication-title: Blood
  doi: 10.1182/blood-2016-06-723940
– volume: 95
  start-page: e5687
  issue: 51
  year: 2016
  ident: 2149_CR47
  publication-title: Medicine
  doi: 10.1097/md.0000000000005687
– volume: 26
  start-page: 107
  issue: 2
  year: 2018
  ident: 2149_CR34
  publication-title: Cardiol Rev
  doi: 10.1097/crd.0000000000000181
– volume: 118
  start-page: 3367
  issue: 12
  year: 2011
  ident: 2149_CR7
  publication-title: Blood
  doi: 10.1182/blood-2010-11-320788
– volume: 115
  start-page: 2490
  issue: 19
  year: 2007
  ident: 2149_CR35
  publication-title: Circulation
  doi: 10.1161/circulationaha.106.667584
– volume: 27
  start-page: 365
  issue: 4
  year: 2016
  ident: 2149_CR15
  publication-title: Platelets
  doi: 10.3109/09537104.2015.1111321
– volume: 14
  start-page: 1179
  issue: 10
  year: 2013
  ident: 2149_CR40
  publication-title: Pharmacogenomics
  doi: 10.2217/pgs.13.108
– volume: 468
  start-page: 459
  issue: 3
  year: 2015
  ident: 2149_CR25
  publication-title: Biochem J
  doi: 10.1042/bj20150192
– volume: 60
  start-page: 1715
  issue: 18
  year: 2012
  ident: 2149_CR43
  publication-title: Am Coll Cardiol
  doi: 10.1016/j.jacc.2011.12.062
– volume: 98
  start-page: 774
  issue: 6
  year: 2006
  ident: 2149_CR30
  publication-title: Am J Cardiol
  doi: 10.1016/j.amjcard.2006.04.015
– volume: 15
  start-page: 45
  issue: 1
  year: 2018
  ident: 2149_CR1
  publication-title: Nat Rev Cardiol
  doi: 10.1038/nrcardio.2017.108
– volume: 10
  start-page: e0138795
  issue: 9
  year: 2015
  ident: 2149_CR44
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0138795
– volume: 133
  start-page: e38
  issue: 4
  year: 2016
  ident: 2149_CR2
  publication-title: Circulation
– volume: 19
  start-page: 1069
  issue: 4
  year: 2018
  ident: 2149_CR37
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms19041069
– volume: 47
  start-page: 1130
  issue: 12
  year: 2017
  ident: 2149_CR8
  publication-title: Xenobiotica
  doi: 10.1080/00498254.2016.1271962
– volume: 19
  start-page: 1
  year: 2018
  ident: 2149_CR23
  publication-title: Platelets
  doi: 10.1080/09537104.2018.1447659
– volume: 119
  start-page: 4056
  issue: 17
  year: 2012
  ident: 2149_CR5
  publication-title: Blood J Am Soc Hematol
– volume: 18
  start-page: 27
  issue: 1
  year: 2014
  ident: 2149_CR3
  publication-title: Hormone Mol Biol Clin Investig
  doi: 10.1515/hmbci-2013-0055
– volume: 140
  start-page: 21
  issue: 1
  year: 2018
  ident: 2149_CR33
  publication-title: Cardiology
  doi: 10.1159/000488101
– volume: 42
  start-page: 608
  issue: 7
  year: 2010
  ident: 2149_CR48
  publication-title: Nat Genet
  doi: 10.1038/ng.604
– volume: 36
  start-page: 228
  issue: 2
  year: 2006
  ident: 2149_CR16
  publication-title: Blood Cells Mol Dis
  doi: 10.1016/j.bcmd.2005.12.026
– volume: 388
  start-page: 141
  year: 2018
  ident: 2149_CR29
  publication-title: J Neurol Sci
  doi: 10.1016/j.jns.2018.03.013
– volume: 18
  start-page: 45
  issue: 1
  year: 2017
  ident: 2149_CR18
  publication-title: BMC Med Genet
  doi: 10.1186/s12881-017-0411-x
– volume: 109
  start-page: 1131
  issue: 6
  year: 2013
  ident: 2149_CR24
  publication-title: Thromb Haemost
  doi: 10.1160/th12-09-0645
– volume: 14
  start-page: 1265
  issue: 5
  year: 2015
  ident: 2149_CR12
  publication-title: Mol Cell Proteomics
  doi: 10.1074/mcp.M114.046946
– volume: 37
  start-page: 1442
  issue: 11
  year: 2016
  ident: 2149_CR46
  publication-title: Acta Pharmacol Sin
  doi: 10.1038/aps.2016.90
– volume: 12
  start-page: e007019
  issue: 5
  year: 2019
  ident: 2149_CR9
  publication-title: Circulation
– volume: 114
  start-page: 1405
  issue: 7
  year: 2009
  ident: 2149_CR19
  publication-title: Blood
  doi: 10.1182/blood-2009-02-202614
– volume: 2018
  start-page: 11976
  year: 1976
  ident: 2149_CR27
  publication-title: Histol Histopathol
– volume: 8
  start-page: e64179
  issue: 5
  year: 2013
  ident: 2149_CR4
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0064179
– volume: 128
  start-page: 1003
  issue: 7
  year: 2016
  ident: 2149_CR45
  publication-title: Blood
  doi: 10.1182/blood-2015-11-682153
– volume: 141
  start-page: 28
  year: 2016
  ident: 2149_CR21
  publication-title: Thromb Res
  doi: 10.1016/j.thromres.2016.02.031
– volume: 6
  start-page: 184
  issue: 2
  year: 2013
  ident: 2149_CR36
  publication-title: Circulation
– volume: 3
  start-page: 275
  issue: 3
  year: 2019
  ident: 2149_CR17
  publication-title: Blood Adv
  doi: 10.1182/bloodadvances.2018024950
– volume: 9
  start-page: 490
  year: 2018
  ident: 2149_CR41
  publication-title: Front Pharmacol
  doi: 10.3389/fphar.2018.00490
– volume: 83
  start-page: 54
  issue: 1
  year: 2019
  ident: 2149_CR11
  publication-title: Ann Hum Genet
  doi: 10.1111/ahg.12285
– ident: 2149_CR28
  doi: 10.1080/10428194.2019.1630622
– volume: 146
  start-page: 76
  year: 2016
  ident: 2149_CR13
  publication-title: Thrombosis Res
  doi: 10.1016/j.thromres.2016.08.026
– volume: 9
  start-page: e111816
  issue: 10
  year: 2014
  ident: 2149_CR32
  publication-title: PLoS ONE
  doi: 10.1371/journal.pone.0111816
– volume: 3
  start-page: 275
  issue: 3
  year: 2019
  ident: 2149_CR26
  publication-title: Blood Adv
  doi: 10.1182/bloodadvances.2018024950
– volume: 163
  start-page: 77
  year: 2018
  ident: 2149_CR39
  publication-title: Thromb Res
  doi: 10.1016/j.thromres.2018.01.026
– volume: 280
  start-page: 24680
  issue: 26
  year: 2005
  ident: 2149_CR10
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M413411200
– volume: 28
  start-page: 1484
  issue: 8
  year: 2008
  ident: 2149_CR31
  publication-title: Arterioscl Thrombo Vasc Biol
  doi: 10.1161/atvbaha.108.168971
– volume: 24
  start-page: 61
  issue: 1
  year: 2015
  ident: 2149_CR42
  publication-title: Blodd Press
  doi: 10.3109/08037051.2014.986928
– ident: 2149_CR6
  doi: 10.1007/s12094-019-02132-9
– volume: 121
  start-page: 5208
  issue: 26
  year: 2013
  ident: 2149_CR14
  publication-title: Blood
  doi: 10.1182/blood-2012-10-462887
– volume: 83
  start-page: 38
  issue: 1
  year: 1991
  ident: 2149_CR20
  publication-title: Caerphilly Collab Heart Dis Stud
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Snippet Platelet Endothelial Aggregation Receptor (PEAR1), as a platelet receptor, plays a vital role in hemostasis. This receptor, by its extracellular part, causes...
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crossref
springer
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StartPage 89
SubjectTerms Cardiology
Cardiovascular diseases
Genetic screening
Hematology
Hemostasis
Homeostasis
Medicine
Medicine & Public Health
Platelet aggregation
Risk factors
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Title PEAR1 polymorphisms as a prognostic factor in hemostasis and cardiovascular diseases
URI https://link.springer.com/article/10.1007/s11239-020-02149-w
https://www.ncbi.nlm.nih.gov/pubmed/32445063
https://www.proquest.com/docview/2480135803
https://www.proquest.com/docview/2406304648
Volume 51
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