UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 53

Sortiert nach

Mechanisms of thrombocytopenia in platelet-type von Willebrand disease

Haematologica (Roma), 2019-07, Vol.104 (7), p.1473-1481

2019

Link zum Volltext

Verfügbarkeit prüfen

A novel mechanism regulating human platelet activation by MMP-2–mediated PAR1 biased signaling

Blood, 2017-02, Vol.129 (7), p.883-895

2017

Link zum Volltext

Verfügbarkeit prüfen

Eltrombopag to allow chemotherapy in a patient with MYH9-related inherited thrombocytopenia and pancreatic cancer

International journal of hematology, 2020-11, Vol.112 (5), p.725-727

2020

Link zum Volltext

Verfügbarkeit prüfen

Learning the Ropes of Platelet Count Regulation: Inherited Thrombocytopenias

Journal of clinical medicine, 2021-02, Vol.10 (3), p.533

2021

Link zum Volltext

Verfügbarkeit prüfen

Search for SARS-CoV-2 RNA in platelets from COVID-19 patients

Platelets (Edinburgh), 2021-02, Vol.32 (2), p.284-287

2021

Link zum Volltext

Verfügbarkeit prüfen

Of mice and men: genes relevant to thrombosis and bleeding

Blood, 2018-12, Vol.132 (24), p.2532-2534

2018

Link zum Volltext

Verfügbarkeit prüfen

Outside-in signalling generated by a constitutively activated integrin αIIbβ3 impairs proplatelet formation in human megakaryocytes

PloS one, 2012, Vol.7 (4), p.e34449-e34449

2012

Link zum Volltext

Verfügbarkeit prüfen

Inherited Platelet Function Disorders: Algorithms for Phenotypic and Genetic Investigation

Seminars in thrombosis and hemostasis, 2016-04, Vol.42 (3), p.292

2016

Link zum Volltext

Verfügbarkeit prüfen

Inherited platelet disorders in women

Thrombosis research, 2019-09, Vol.181, p.S54-S59

2019

Link zum Volltext

Verfügbarkeit prüfen

Association of Neutrophil Activation, More Than Platelet Activation, With Thrombotic Complications in Coronavirus Disease 2019

The Journal of infectious diseases, 2021-03, Vol.223 (6), p.933-944

2021

Link zum Volltext

Verfügbarkeit prüfen

Usefulness of global tests of primary hemostasis in the initial screening of mild/moderate bleeding disorders for orienting towards von Willebrand disease or inherited platelet functions disorders

Thrombosis research, 2023-01, Vol.221, p.79-82

2023

Link zum Volltext

Verfügbarkeit prüfen

Platelet dysfunction in platelet-type von Willebrand disease due to the constitutive triggering of the Lyn-PECAM1 inhibitory pathway

Haematologica (Roma), 2022-07, Vol.107 (7), p.1643-1654

2022

Link zum Volltext

Verfügbarkeit prüfen

Megakaryocytes differentially sort mRNAs for matrix metalloproteinases and their inhibitors into platelets: a mechanism for regulating synthetic events

Blood, 2011-08, Vol.118 (7), p.1903-1911

2011

Link zum Volltext

Verfügbarkeit prüfen

Platelet function assays in diagnosis: an update

Expert review of hematology, 2019-01, Vol.12 (1), p.29-46

2019

Link zum Volltext

Verfügbarkeit prüfen

Prochemerin cleavage by factor XIa links coagulation and inflammation

Blood, 2018-01, Vol.131 (3), p.353-364

2018

Link zum Volltext

Verfügbarkeit prüfen

Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH

Journal of thrombosis and haemostasis, 2019-08, Vol.17 (8), p.1253-1260

2019

Link zum Volltext

Verfügbarkeit prüfen

Increase of von Willebrand factor with aging in type 1 von Willebrand disease: fact or fiction?

Haematologica (Roma), 2017-11, Vol.102 (11), p.e431-e433

2017

Link zum Volltext

Verfügbarkeit prüfen

Germline GATA2 variant disrupting endothelial eNOS function and angiogenesis can be restored by c-Jun/AP-1 upregulation

Haematologica (Roma), 2022-05, Vol.107 (5), p.1072-1085

2022

Link zum Volltext

Verfügbarkeit prüfen

Inherited platelet function disorders. Diagnostic approach and management

Hämostaseologie, 2016, Vol.36 (4), p.265

2016

Link zum Volltext

Verfügbarkeit prüfen

Role of endothelial dysfunction in the thrombotic complications of COVID-19 patients

The Journal of infection, 2021-05, Vol.82 (5), p.186-230

2021

Link zum Volltext

Verfügbarkeit prüfen

GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis

Journal of thrombosis and haemostasis, 2021-10, Vol.19 (10), p.2612-2617

2021

Link zum Volltext

Verfügbarkeit prüfen

Cytoskeletal perturbation leads to platelet dysfunction and thrombocytopenia in variant forms of Glanzmann thrombasthenia

Haematologica (Roma), 2016-01, Vol.101 (1), p.46-56

2016

Link zum Volltext

Verfügbarkeit prüfen

Possible incorrect genotyping of heterozygous factor V Leiden and Prothrombin 20210 gene mutations by the GeneXpert assay

Clinica chimica acta, 2014-08, Vol.435, p.36-39

2014

Link zum Volltext

Verfügbarkeit prüfen

A novel variant Glanzmann thrombasthenia due to co-inheritance of a loss- and a gain-of-function mutation of ITGB3 : evidence of a dominant effect of gain-of-function mutations

Haematologica (Roma), 2018-06, Vol.103 (6), p.e259-e263

2018

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 53

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(49)
Mit Volltextzugriff
(47)

Publikationsform

Artikel
(49)
Berichte
(4)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Mechanisms of thrombocytopenia in platelet-type von Willebrand disease

A novel mechanism regulating human platelet activation by MMP-2–mediated PAR1 biased signaling

Eltrombopag to allow chemotherapy in a patient with MYH9-related inherited thrombocytopenia and pancreatic cancer

Learning the Ropes of Platelet Count Regulation: Inherited Thrombocytopenias

Search for SARS-CoV-2 RNA in platelets from COVID-19 patients

Of mice and men: genes relevant to thrombosis and bleeding

Outside-in signalling generated by a constitutively activated integrin αIIbβ3 impairs proplatelet formation in human megakaryocytes

Inherited Platelet Function Disorders: Algorithms for Phenotypic and Genetic Investigation

Inherited platelet disorders in women

Association of Neutrophil Activation, More Than Platelet Activation, With Thrombotic Complications in Coronavirus Disease 2019

Usefulness of global tests of primary hemostasis in the initial screening of mild/moderate bleeding disorders for orienting towards von Willebrand disease or inherited platelet functions disorders

Platelet dysfunction in platelet-type von Willebrand disease due to the constitutive triggering of the Lyn-PECAM1 inhibitory pathway

Megakaryocytes differentially sort mRNAs for matrix metalloproteinases and their inhibitors into platelets: a mechanism for regulating synthetic events

Platelet function assays in diagnosis: an update

Prochemerin cleavage by factor XIa links coagulation and inflammation

Curated disease‐causing genes for bleeding, thrombotic, and platelet disorders: Communication from the SSC of the ISTH

Increase of von Willebrand factor with aging in type 1 von Willebrand disease: fact or fiction?

Germline GATA2 variant disrupting endothelial eNOS function and angiogenesis can be restored by c-Jun/AP-1 upregulation

Inherited platelet function disorders. Diagnostic approach and management

Role of endothelial dysfunction in the thrombotic complications of COVID-19 patients

Bleeding risk of surgery and its prevention in patients with inherited platelet disorders

GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis

Cytoskeletal perturbation leads to platelet dysfunction and thrombocytopenia in variant forms of Glanzmann thrombasthenia

Possible incorrect genotyping of heterozygous factor V Leiden and Prothrombin 20210 gene mutations by the GeneXpert assay

A novel variant Glanzmann thrombasthenia due to co-inheritance of a loss- and a gain-of-function mutation of ITGB3 : evidence of a dominant effect of gain-of-function mutations

Suchergebnisse filtern