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UnknownIdentification and characterization of the elusive mutation causing the historical von Willebrand Disease type IIC Miami.
Not available
S-EPMC5035592 | biostudies-literature
UnknownGermline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.
Not available
S-EPMC2820190 | biostudies-literature
UnknownEnhanced Local Disorder in a Clinically Elusive von Willebrand Factor Provokes High-Affinity Platelet Clumping.
Not available
S-EPMC5839150 | biostudies-literature
UnknownThe mutation N528S in the von Willebrand factor (VWF) propeptide causes defective multimerization and storage of VWF.
Not available
S-EPMC2881501 | biostudies-literature
UnknownAn international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF study.
Not available
S-EPMC6292779 | biostudies-literature
UnknownAdvancing multimer analysis of von Willebrand factor by single-molecule AFM imaging.
Not available
S-EPMC6333368 | biostudies-literature
UnknownUpshaw-Schulman syndrome-associated ADAMTS13 variants possess proteolytic activity at the surface of endothelial cells and in simulated circulation.
Not available
S-EPMC7197795 | biostudies-literature
UnknownAldosterone exerts anti-inflammatory effects on LPS stimulated microglia.
Not available
S-EPMC6174543 | biostudies-literature
UnknownVon Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS-IPS study.
Not available
S-EPMC9305521 | biostudies-literature
UnknownExponential size distribution of von Willebrand factor.
Not available
S-EPMC3762346 | biostudies-literature
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