Search results (208)
« Back to PublicationsCDIN1-Codanin-1 complex defective in congenital dyserythropoietic anaemia type I is an RNA nuclease.
Brolih S. et al, (2026), Nat Commun
Automated LLM Deployment and Evaluation: A Cloud-Native Approach Using LLM-as-a-Judge
Rafique A. and Marsden BD., (2025), IEEE International Conference on Cloud Computing Cloud, 448 - 450
Discovery and characterization of potent inhibitors of the RNA editing enzyme ADAR1
Pollard J. et al, (2024), EUROPEAN JOURNAL OF CANCER, 211, S37 - S37
Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank
Lassen FH. et al, (2024), EUROPEAN JOURNAL OF HUMAN GENETICS, 32, 851 - 852
USP18 A NOVEL REGULATOR OF MUSCLE CELL DIFFERENTIATION AND MATURATION, POTENTIALLY REGULATING REGENERATION IN DERMATOMYOSITIS
Olie CS. et al, (2023), CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 41, 446 - 446
A Multi-omics Approach at the Tissue and Single-Cell Level Provides New Insight into the Pathomechanisms of Uterine Fibroids and Associated Heavy Menstrual Bleeding
Philpott M. et al, (2023), REPRODUCTIVE SCIENCES, 30, 207A - 208A
Integrated Transcriptomic and Proteomic Profiling of Responses to Clinical and Novel Bisphosphonates Reveal Extraskeletal Effects and Protection Against Senescence
Lu J. et al, (2023), JOURNAL OF BONE AND MINERAL RESEARCH, 38, 426 - 426
Venus: Elucidating the impact of amino acid variants on protein function beyond structure destabilisation
Ferla M. et al, (2023), EUROPEAN JOURNAL OF HUMAN GENETICS, 31, 614 - 614
Normothermic machine perfusion following prior static cold storage has a similar molecular profile to continuous NMP, with more sensitivity to ex situ reperfusion injury
Dengu F. et al, (2023), TRANSPLANTATION, 107, 40 - 40
Elevator mechanism dynamics in a sodium-coupled dicarboxylate transporter
Kinz-Thompson C. et al, (2023), PROTEIN SCIENCE, 32
Interactome screening of C9orf72 dipeptide repeats reveals VCP sequestration and functional impairment by polyGA.
Božič J. et al, (2022), Brain, 145, 684 - 699
The first human importin-β-related disorder: syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8
Van Gucht I. et al, (2022), EUROPEAN JOURNAL OF HUMAN GENETICS, 30, 5 - 6
A Single-Cell Atlas of the Leiomyoma Vascular Capsule Reveals Activation of Endothelial and Immune Cells
Philpott M. et al, (2022), REPRODUCTIVE SCIENCES, 29, 205 - 205
USP19 Inhibition Affects Adipogenesis, Reflecting a Novel Target in Obesity and Female-Specific Cardiometabolic Traits
O'Brien DP. et al, (2022), REPRODUCTIVE SCIENCES, 29, 239 - 239
Targeted Delivery of Galunisertib Attenuates Fibrogenesis in an Integrated Ex Vivo Renal Transplant and Fibrosis Model
Van Leeuwen L. et al, (2022), TRANSPLANTATION, 106, S234 - S234