Results 181 to 190 of about 1,012,097 (266)

Autophagosome marker, LC3, is released extracellularly via several distinct pathways

FEBS Open Bio, EarlyView.
This study establishes a novel HiBiT‐tagging system for ultrasensitive detection of LC3, revealing multiple pathways for its extracellular secretion. It demonstrates that LC3 is released via both autophagy‐dependent and ‐independent mechanisms, including a novel route for nonlipidated LC3‐I.
Koki Saito, Masashi Arakawa, Koki Maeda, Eiji Morita   +3 more
wiley   +1 more source

Anesthetic Management for the Patient with Coagulation Factor X Deficiency.

, 1998
Koichi Mori, Kazunori Kawamura, Shinya Hori, Akira Tanaka   +3 more
openalex   +2 more sources

HTRS2023.P2.7 Burden of disease and impact on quality of life in hereditary factor X deficiency patients receiving prophylaxis: findings from the Hereditary Factor X Deficiency in America survey

, 2023
Denise Garner, Kim Clark, Shirley P. Huang, Richard H. Stanford, Brian R. Branchford   +4 more
openalex   +1 more source

Analysis of Treacher Collins syndrome 4‐associated mutations in Schizosaccharomyces pombe

FEBS Open Bio, EarlyView.
Fission yeast models carrying Treacher Collins syndrome type 4‐associated mutations reveal that impaired processivity of RNA polymerase I leads to defective rRNA transcription. This study highlights the essential role of a conserved arginine residue in Pol I elongation and provides mechanistic insight into the pathogenesis of ribosomopathies.
Kei Kawakami, Hiroaki Kato
wiley   +1 more source

HTRS2025.P1.47 Procoagulant Enhancement of Inherited Factor X Deficiency with Emicizumab

Research and Practice in Thrombosis and Haemostasis
Kyumin Lee, Annalisse DeSandre, Sebastian E. Leyes Porello, Rodney M. Camire, Benjamin J. Samelson-Jones   +4 more
doaj   +1 more source

Rare case of combined factor V and factor X deficiency in pregnancy: presenting as secondary postpartum haemorrhage in first pregnancy and successful outcome in second pregnancy

, 2012
Aniket Kakade, Tushar Panchanadikar, Yashwant S. Kulkarni   +2 more
openalex   +1 more source

Molecular defect (Gla+ 14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X" Vorarlberg").

, 2021
Herbert Watzke, Klaus Lechner, Harold R. Roberts, Sakamuri V. Reddy, Dean J. Welsch, Paul A. Friedman, Gert Mahr, Pudur Jagadeeswaran, Dougald M. Monroe, Katherine A. High   +9 more
openalex   +1 more source

Hands‐on protocol for preparing water‐soluble fractions from agri‐food samples for NMR‐based metabolomics analysis

FEBS Open Bio, EarlyView.
This research protocol outlines a workflow for nuclear magnetic resonance (NMR)‐based metabolomics in the agri‐food sector. Using two case studies—strawberry leaves (solid matrix) and wine (liquid matrix)—it details the procedures for sample preparation, data acquisition, and processing.
Andrea Fernández‐Veloso, Jaime Hiniesta‐Valero, Alejandra Guerra‐Castellano, Miguel A. De la Rosa, Irene Díaz‐Moreno   +4 more
wiley   +1 more source

Utility of factor X concentrate for the treatment of acquired factor X deficiency in systemic light-chain amyloidosis [PDF]

, 2014
Shameem Mahmood, Julie Blundell, Anja Drebes, Philip N. Hawkins, Ashutosh Wechalekar   +4 more
openalex   +1 more source

DDX3X induces mesenchymal transition of endothelial cells by disrupting BMPR2 signaling

FEBS Open Bio, EarlyView.
Elevated DDX3X expression led to downregulation of BMPR2, a key regulator of endothelial homeostasis and function. Our co‐immunoprecipitation assays further demonstrated a molecular interaction between DDX3X and BMPR2. Notably, DDX3X promoted lysosomal degradation of BMPR2, thereby impairing its downstream signaling and facilitating endothelial‐to ...
Yu Zhang, Jing Wang, De‐Hui Qian, Yang‐Fan Lv, Tian‐Le Cheng, Da‐Peng Wang, Jing Zhang, Ye Fan   +7 more
wiley   +1 more source