Topic · Pulmonary and Respiratory Medicine · Medicine
Blood properties and coagulation
OpenAlex topic; a paper is listed when OpenAlex scores it at least 0.5 for this topic.
38 papers
Proteomic evidence for amyloidogenic cross-seeding in fibrinaloid microclots
Douglas Bruce Kell, Etheresia Pretorius
The paper provides proteomic evidence that fibrinaloid microclots involve cross-seeding of non-fibrin proteins into amyloid structures, suggesting a complex mechanism beyond simple entrapment.
International Journal of Molecular Sciences · Oct 8, 2024Peer-reviewedBiochemistry
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
Jennifer E. Huffman, Jayna C. Nicholas, Julie M. Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek, Jennifer A. Brody, Florian Thibord, Laura A. Almasy, Traci M. Bartz, Lawrence F. Bielak, Russell Paul Bowler, Germán D. Carrasquilla, Daniel I. Chasman, Ming‐Huei Chen, , Yoav Ben‐Shlomo
This study uses whole genome sequencing to identify 18 novel genetic loci associated with plasma fibrinogen levels, including variants more common in African populations and linked to liver-related traits and disease.
Blood · Sep 3, 2024Peer-reviewedGenetic & Genomic Medicine
The chromatin-remodeling enzyme Smarca5 regulates erythrocyte aggregation via Keap1-Nrf2 signaling
Yanyan Ding, Yuzhe Li, Ziqian Zhao, Qiangfeng Cliff Zhang, Feng Liu
This study shows that Smarca5 regulates erythrocyte aggregation through Keap1-Nrf2 signaling in zebrafish, leading to venous thrombosis-like phenotypes.
eLife · Oct 26, 2021Peer-reviewedDevelopmental Biology
Association between erythrocyte dynamics and vessel remodelling in developmental vascular networks
Qi Zhou, Tijana Perovic, Ines Fechner, Lowell T. Edgar, Peter R. Hoskins, Holger Gerhardt, Timm Krüger, Miguel O. Bernabéu
The paper investigates how erythrocyte dynamics influence vascular remodelling in developing networks, finding that RBC depletion correlates with vessel regression and that plasma skimming drives this process.
Journal of The Royal Society Interface · Jun 1, 2021Peer-reviewedDevelopmental Biology
A novel fibrinogen gamma-chain mutation, p. γAla327Val, causes structural abnormality of D region and ultimately leads to congenital dysfibrinogenemia
Aiqiu Wei, Yangyang Wu, Liqun Xiang, Jie Yan, Peng Cheng, Donghong Deng, Faquan Lin
This study identifies a novel γAla327Val mutation in the FGG gene causing congenital dysfibrinogenemia by altering fibrinogen structure and function.
bioRxiv · Jan 29, 2020 · PreprintMolecular Biology
The plasma Factor XIII heterotetrameric complex structure: unexpected unequal pairing within a symmetric complex
Sneha Singh, Alexis Nazabal, Senthilvelrajan Kaniyappan, Jean‐Luc Pellequer, Alisa S. Wolberg, Diana Imhof, Johannes Oldenburg, Arijit Biswas
The paper determines the structure of the FXIII-A2B2 complex, revealing asymmetric subunit pairing critical for its assembly and activation.
Biomolecules · Nov 21, 2019Peer-reviewedMolecular Biology
Lipopolysaccharide-binding protein (LBP) can reverse the amyloid state of fibrin seen or induced in Parkinson’s disease: implications for its aetiology
Etheresia Pretorius, Martin Pagé, Sthembile Mbotwe, Douglas Bruce Kell
The paper shows that LBP prevents fibrin from adopting an amyloid form induced by LPS, suggesting a link between microbial products and Parkinson’s disease.
PLoS ONE · Mar 1, 2018Peer-reviewedNeuroscience