Beth G. Gibson
Newcastle Upon Tyne, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 13 publications
Properdin deficiency or anti-properdin treatment ameliorates disease in the C3 gain-of-function mouse model of atypical haemolytic uraemic syndrome.
Journal: Frontiers in immunology
Published: March 11, 2026
Biallelic pathogenic variants in EXOSC3 mediate renal thrombotic microangiopathy of the kidney.
Journal: Kidney international
Published: February 10, 2026
Contrast-Enhanced Ultrasound to Assess Kidney Quality During Ex Situ Normothermic Machine Perfusion.
Contrast-Enhanced Ultrasound to Assess Kidney Quality During Ex Situ Normothermic Machine Perfusion.
Journal: Transplant international : official journal of the European Society for Organ Transplantation
Published: December 29, 2024
Deep learning for automated boundary detection and segmentation in organ donation photography.
Journal: Innovative surgical sciences
Published: May 21, 2024
Contribution of animal models to the mechanistic understanding of Alternative Pathway and Amplification Loop (AP/AL)-driven Complement-mediated Diseases.
Journal: Immunological reviews
Published: October 07, 2022
Homodimeric Minimal Factor H: In Vivo Tracking and Extended Dosing Studies in Factor H Deficient Mice.
Journal: Frontiers in immunology
Published: August 03, 2021
Insights Into the Structure-Function Relationships of Dimeric C3d Fragments.
Journal: Frontiers in immunology
Published: May 24, 2021
Investigating Evolutionary Rate Variation in Bacteria.
Journal: Journal of molecular evolution
Published: November 12, 2018
Calcium activated nucleotidase 1 (CANT1) is critical for glycosaminoglycan biosynthesis in cartilage and endochondral ossification.
Journal: Matrix biology : journal of the International Society for Matrix Biology
Published: September 21, 2018
The distribution of bacterial doubling times in the wild.
Journal: Proceedings. Biological sciences
Published: April 09, 2018
The aggrecanopathies; an evolving phenotypic spectrum of human genetic skeletal diseases.
Journal: Orphanet journal of rare diseases
Published: January 09, 2016
Last Updated: 09/26/2026