Results 261 to 270 of about 185,950 (370)
von Willebrand factor propeptide and the phenotypic classification of von Willebrand disease.
Y. Sanders +11 more
semanticscholar +1 more source
Endothelial Effects in the Elderly: Fibroblast Regulation in Soft Tissue Healing
ABSTRACT Two main influencing factors of human soft tissue healing are concomitant diseases and cellular senescence, both accumulating with increasing age. Due to the raising population of the elderly in western countries, it is essential to enhance the level of knowledge concerning the function of senescence in a granulation tissue during repair.
Martin Oberringer +4 more
wiley +1 more source
Delayed epidural hematoma after spinal cord stimulator implantation in a patient with von Willebrand disease: Illustration. [PDF]
Jaffee S +4 more
europepmc +1 more source
Single-domain antibodies for brain targeting [PDF]
Lalatsa, Katerina, Moreira Leite, Diana
core +1 more source
The Lrs14‐Like AbfR1 Homolog From Metallosphaera sedula Is a Nucleoid‐Organizing Protein
Nucleoid organization in Crenarchaeota involves diverse small DNA‐binding proteins. The Lrs14‐type protein AbfR1 from Metallosphaera sedula binds nonsequence specifically across the genome and induces DNA condensation. These findings suggest a structural role for AbfR1Ms in chromatin architecture, functionally resembling bacterial nucleoid‐associated ...
Veerke De Kock +5 more
wiley +1 more source
Challenges and considerations of genetic testing in von Willebrand disease. [PDF]
Seidizadeh O, Baronciani L, Peyvandi F.
europepmc +1 more source
Complications at Diagnosis of Pediatric Chronic Myeloid Leukemia in Chronic Phase
ABSTRACT Chronic myeloid leukemia (CML) is uncommon during the first two decades of life, resulting in limited experience of pediatricians in handling this leukemia. This is even more true when it comes to managing rare complications at the time of diagnosis.
Nirmalya Roy Moulik +4 more
wiley +1 more source
Laboratory diagnosis of von Willebrand disease
Jonathan C Roberts, V. Flood
semanticscholar +1 more source
ABSTRACT Congenital thrombotic thrombocytopenic purpura (cTTP) is an ultra‐rare, life‐threatening thrombotic microangiopathy caused by a severe inherited deficiency of ADAMTS13, a von Willebrand factor (VWF) cleaving enzyme. Inadequate clinical endpoint data often make it challenging to statistically power clinical trials in ultra‐rare diseases ...
Cameron McBride +8 more
wiley +1 more source

