UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 71

Sortiert nach

The activity of the intrinsically water-soluble enzyme ADAMTS13 correlates with the membrane state when bound to a phospholipid bilayer

Scientific reports, 2021-12, Vol.11 (1), p.24476-24476, Article 24476

2021

Volltextzugriff (PDF)

Shear-Induced Unfolding and Enzymatic Cleavage of Full-Length VWF Multimers

Biophysical journal, 2016-02, Vol.110 (3), p.545-554

2016

Volltextzugriff (PDF)

Nonsense Mutation and Inactivation of SMARCA4 (BRG1) in an Atypical Teratoid/Rhabdoid Tumor Showing Retained SMARCB1 (INI1) Expression

The American journal of surgical pathology, 2011-06, Vol.35 (6), p.933-935

2011

Volltextzugriff (PDF)

Interaction of von Willebrand factor domains with collagen investigated by single molecule force spectroscopy

The Journal of chemical physics, 2018-03, Vol.148 (12), p.123310-123310

2018

Volltextzugriff (PDF)

Force sensing by the vascular protein von Willebrand factor is tuned by a strong intermonomer interaction

Proceedings of the National Academy of Sciences - PNAS, 2016-02, Vol.113 (5), p.1208-1213

2016

Volltextzugriff (PDF)

The von Willebrand factor Tyr2561 allele is a gain-of-function variant and a risk factor for early myocardial infarction

Blood, 2019-01, Vol.133 (4), p.356-365

2019

Volltextzugriff (PDF)

Upshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation

PloS one, 2020-05, Vol.15 (5), p.e0232637-e0232637

2020

Volltextzugriff (PDF)

Performance evaluation and multicentre study of a von Willebrand factor activity assay based on GPIb binding in the absence of ristocetin

Blood coagulation & fibrinolysis, 2014-12, Vol.25 (8), p.860-870

2014

Volltextzugriff (PDF)

von Willebrand factor is dimerized by protein disulfide isomerase

Blood, 2016-03, Vol.127 (9), p.1183-1191

2016

Volltextzugriff (PDF)

pH-Dependent Interactions in Dimers Govern the Mechanics and Structure of von Willebrand Factor

Biophysical journal, 2016-07, Vol.111 (2), p.312-322

2016

Volltextzugriff (PDF)

von Willebrand disease type 2A phenotypes IIC, IID and IIE: A day in the life of shear-stressed mutant von Willebrand factor

Thrombosis and haemostasis, 2014, Vol.112 (1), p.96

2014

Volltextzugriff (PDF)

Von Willebrand Factor Mediates Pneumococcal Aggregation and Adhesion in Blood Flow

Frontiers in microbiology, 2019-03, Vol.10, p.511-511

2019

Volltextzugriff (PDF)

Platelet adhesion and aggregate formation controlled by immobilised and soluble VWF

BMC molecular and cell biology, 2020-09, Vol.21 (1), p.64-64, Article 64

2020

Volltextzugriff (PDF)

Space and Time Resolved Detection of Platelet Activation and von Willebrand Factor Conformational Changes in Deep Suspensions

International journal of biomedical imaging, 2017-01, Vol.2017, p.8318906-13

2017

Volltextzugriff (PDF)

Multiplexed protein force spectroscopy reveals equilibrium protein folding dynamics and the low-force response of von Willebrand factor

Proceedings of the National Academy of Sciences - PNAS, 2019-09, Vol.116 (38), p.18798-18807

2019

Volltextzugriff (PDF)

Single molecule force spectroscopy data and BD- and MD simulations on the blood protein von Willebrand factor

Data in brief, 2016-09, Vol.8, p.1080-1087

2016

Volltextzugriff (PDF)

von Willebrand factor directly interacts with DNA from neutrophil extracellular traps

Arteriosclerosis, thrombosis, and vascular biology, 2014-07, Vol.34 (7), p.1382

2014

Volltextzugriff (PDF)

Medulloblastoma in children with Fanconi anemia: Association with FA-D1/FA-N, SHH type and poor survival independent of treatment strategies

Neuro-oncology (Charlottesville, Va.), 2024-06

2024

Volltextzugriff (PDF)

NFS-03. MEDULLOBLASTOMA IN CHILDREN WITH FANCONI ANEMIA: ASSOCIATION WITH FA-D1/FA-N, SHH TYPE AND POOR SURVIVAL INDEPENDENT OF TREATMENT STRATEGIES

Neuro-oncology (Charlottesville, Va.), 2024-06, Vol.26 (Supplement_4), p.0-0

2024

Volltextzugriff (PDF)

Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand disease

Blood, 2001-04, Vol.97 (7), p.2059-2066

2001

Volltextzugriff (PDF)

The search for the underlying mutations causing VWD in 13 Venezuelan families

Thrombosis research, 2024-03, Vol.235, p.88-91

2024

Volltextzugriff (PDF)

The Low-Force Response of Von Willebrand Factor Revealed by Magnetic Tweezers

Biophysical journal, 2020-02, Vol.118 (3), p.619a-620a

2020

Volltextzugriff (PDF)

Heparan sulfate dependent binding of plasmatic von Willebrand factor to blood circulating melanoma cells attenuates metastasis

Matrix biology, 2022-08, Vol.111, p.76-94

2022

Volltextzugriff (PDF)

Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations

Thrombosis and haemostasis, 2019-07, Vol.119 (7), p.1102

2019

Volltextzugriff (PDF)

Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome

American journal of human genetics, 2010-02, Vol.86 (2), p.279-284

2010

Volltextzugriff (PDF)

1 – 25 von 71

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(71)
Mit Volltextzugriff
(64)

Publikationsform

Artikel
(71)

Sprache

Englisch
(71)
Japanisch
(9)

Erscheinungsjahr

n.n

Thema

Science & Technology
(40)
Life Sciences & Biomedicine
(32)
Humans
(30)
Hematology
(20)
Von Willebrand Factor
(20)
Von Willebrand Factor - Metabolism
(18)
Von Willebrand Factor - Chemistry
(17)
Von Willebrand Factor - Genetics
(14)
Biological And Medical Sciences
(12)
Medical Sciences
(12)
Male
(11)
Female
(10)
Mutation
(10)
Cardiovascular System & Cardiology
(9)
Hematologic And Hematopoietic Diseases
(9)
Peripheral Vascular Disease
(9)
Amino Acid Substitution
(8)
Phenotype
(8)
Adamts13 Protein
(7)
Child
(7)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

The activity of the intrinsically water-soluble enzyme ADAMTS13 correlates with the membrane state when bound to a phospholipid bilayer

Shear-Induced Unfolding and Enzymatic Cleavage of Full-Length VWF Multimers

Nonsense Mutation and Inactivation of SMARCA4 (BRG1) in an Atypical Teratoid/Rhabdoid Tumor Showing Retained SMARCB1 (INI1) Expression

Interaction of von Willebrand factor domains with collagen investigated by single molecule force spectroscopy

Force sensing by the vascular protein von Willebrand factor is tuned by a strong intermonomer interaction

The von Willebrand factor Tyr2561 allele is a gain-of-function variant and a risk factor for early myocardial infarction

Upshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation

Performance evaluation and multicentre study of a von Willebrand factor activity assay based on GPIb binding in the absence of ristocetin

von Willebrand factor is dimerized by protein disulfide isomerase

pH-Dependent Interactions in Dimers Govern the Mechanics and Structure of von Willebrand Factor

von Willebrand disease type 2A phenotypes IIC, IID and IIE: A day in the life of shear-stressed mutant von Willebrand factor

Von Willebrand Factor Mediates Pneumococcal Aggregation and Adhesion in Blood Flow

Platelet adhesion and aggregate formation controlled by immobilised and soluble VWF

Space and Time Resolved Detection of Platelet Activation and von Willebrand Factor Conformational Changes in Deep Suspensions

Multiplexed protein force spectroscopy reveals equilibrium protein folding dynamics and the low-force response of von Willebrand factor

Single molecule force spectroscopy data and BD- and MD simulations on the blood protein von Willebrand factor

von Willebrand factor directly interacts with DNA from neutrophil extracellular traps

Medulloblastoma in children with Fanconi anemia: Association with FA-D1/FA-N, SHH type and poor survival independent of treatment strategies

NFS-03. MEDULLOBLASTOMA IN CHILDREN WITH FANCONI ANEMIA: ASSOCIATION WITH FA-D1/FA-N, SHH TYPE AND POOR SURVIVAL INDEPENDENT OF TREATMENT STRATEGIES

Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand disease

The search for the underlying mutations causing VWD in 13 Venezuelan families

The Low-Force Response of Von Willebrand Factor Revealed by Magnetic Tweezers

Heparan sulfate dependent binding of plasmatic von Willebrand factor to blood circulating melanoma cells attenuates metastasis

Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations

Germline Nonsense Mutation and Somatic Inactivation of SMARCA4/BRG1 in a Family with Rhabdoid Tumor Predisposition Syndrome

Suchergebnisse filtern