[HTML][HTML] MicroRNAs as prognostic biomarkers for (cancer–associated) venous thromboembolism

RJS Anijs, YN Nguyen, SC Cannegieter… - Journal of Thrombosis …, 2023 - Elsevier
MicroRNAs (miRNAs) are small noncoding RNAs with gene regulatory functions and are
commonly dysregulated in disease states. As miRNAs are relatively stable, easily measured …

Post-transcriptional control of haemostatic genes: mechanisms and emerging therapeutic concepts in thrombo-inflammatory disorders

S Danckwardt, DA Trégouët… - Cardiovascular …, 2023 - academic.oup.com
The haemostatic system is pivotal to maintaining vascular integrity. Multiple components
involved in blood coagulation have central functions in inflammation and immunity. A …

Role of microRNAs in hemophilia and thrombosis in humans

KI Jankowska, ZE Sauna, CD Atreya - International journal of molecular …, 2020 - mdpi.com
MicroRNAs (miRNA) play an important role in gene expression at the posttranscriptional
level by targeting the untranslated regions of messenger RNA (mRNAs). These small RNAs …

[HTML][HTML] Human platelet concentrates treated with microbicidal 405 nm light retain hemostasis activity

JW Jackson, PR Kaldhone, LA Parunov… - … of Photochemistry and …, 2024 - Elsevier
Chemical and UV light-based pathogen reduction technologies are currently in use for
human platelet concentrates (PCs) to enhance safety from transfusion-transmitted infections …

Endothelial dysfunction and atherosclerosis related miRNA‐expression in patients with haemophilia

S Noone, R Schubert, S Fichtlscherer, T Hilberg… - …, 2023 - Wiley Online Library
Introduction Elevated markers of endothelial dysfunction and inflammation indicate worse
endothelial function in the aging haemophilia population. MicroRNAs (miRNAs) regulate …

Whole F8 gene sequencing combined with splicing functional analyses led to a substantial increase of the molecular diagnosis yield for non‐severe haemophilia A

A Dericquebourg, M Fretigny, A Leuci… - …, 2023 - Wiley Online Library
Introduction Conventional genetic investigation fails to identify the F8 causal variant in 2.5%‐
10% of haemophilia A (HA) patients with non‐severe phenotypes. In these cases, F8 deep …

The challenge of genetically unresolved haemophilia A patients: Interest of the combination of whole F8 gene sequencing and functional assays

F Lassalle, Y Jourdy, L Jouan, L Swystun… - …, 2020 - Wiley Online Library
Background The causative variant remains unidentified in 2%–5% of haemophilia A (HA)
patients despite an exhaustive sequencing of the full F8 coding sequence, splice consensus …

RNA sequencing suggests that non‐coding RNAs play a role in the development of acquired haemophilia

AB Tigu, I Hotea, R Drula, AA Zimta… - Journal of Cellular …, 2023 - Wiley Online Library
Acquired haemophilia (AH) is a rare disorder characterized by bleeding in patients with no
personal or family history of coagulation/clotting‐related diseases. This disease occurs …

The role of microRNAs in defining LSECs cellular identity and in regulating F8 gene expression

MA Jamil, R Al-Rifai, N Nuesgen, J Altmüller… - Frontiers in …, 2024 - frontiersin.org
Introduction: Coagulation Factor VIII (FVIII) plays a pivotal role in the coagulation cascade,
and deficiencies in its levels, as seen in Hemophilia A, can lead to significant health …

Further Evidence That MicroRNAs Can Play a Role in Hemophilia A Disease Manifestation: F8 Gene Downregulation by miR-19b-3p and miR-186-5p

KI Jankowska, J McGill, B Pezeshkpoor… - Frontiers in Cell and …, 2020 - frontiersin.org
Hemophilia A (HA) is a F8 gene mutational disorder resulting in deficiency or dysfunctional
FVIII protein. However, surprisingly, in few cases, HA is manifested even without mutations …