Results 161 to 170 of about 69,458 (313)
Non‐canonical PKG1 regulation in cardiovascular health and disease
It is well established that the cyclic GMP‐dependent protein kinase I (PKG1) is canonically activated by cyclic guanosine monophosphate (cGMP), enabling its regulation of vascular tone, cardiac function and smooth muscle homeostasis. However, diverse non‐canonical stimuli of PKG1 have also been identified.
Jie Su, Joseph Robert Burgoyne
wiley +1 more source
The role of platelet membrane proteins in the interaction of platelet-vWF-collagen.
Morio Aihara+7 more
openalex +2 more sources
C1qTNF–related protein-1 (CTRP-1): a vascular wall protein that inhibits collagen-induced platelet aggregation by blocking VWF binding to collagen [PDF]
Gerald Lasser+8 more
openalex +1 more source
This study investigates the intratumoral heterogeneity (ITH) in osteosarcoma by analyzing paired tumor tissue samples from the central and peripheral regions of six patients using single‐cell RNA sequencing. The findings reveal significant microenvironmental differences, with the central region enriched in immune cells and the peripheral region ...
Zhehao Dai+7 more
wiley +1 more source
Botrocetin/VWF-induced signaling through GPIb-IX-V produces TxA2 in an αIIbβ3- and aggregation-independent manner [PDF]
Junling Liu+4 more
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FKBP5 Mediates Alveolar Fibroblast Necroptosis During Acute Respiratory Distress Syndrome
Structure diagram of alveolar fibroblast activation in septic ARDS model. FKBP5‐mediated alveolar fibroblast necroptosis, leading to the activation of NF‐κB signalling and the secretion of cytokines and the recruitment of neutrophils, and further orchestrating the inflammatory environment of the alveolar epithelia in septic ARDS.
Dong Zhang+9 more
wiley +1 more source
Challenges and considerations of genetic testing in von Willebrand disease
von Willebrand disease (VWD) is the most common inherited bleeding disorder characterized by defects in the quantity or function of the von Willebrand factor (VWF).
Omid Seidizadeh+2 more
doaj
Fatal relapse of thrombotic thrombocytopaenic purpura after cardiac surgery in patient with congenital absence of vWF-cleaving protease activity [PDF]
Nikolina Bašić‐Jukić+2 more
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ABSTRACT Introduction Jacobsen syndrome, resulting from a terminal deletion of chromosome 11 (11q), may lead to an increased bleeding tendency due to low platelet counts or platelet dysfunction. Currently, information on bleeding tendency and platelet function in patients with nonterminal 11q‐aberrations such as larger deletions, interstitial 11q ...
Elise J. Huisman+10 more
wiley +1 more source