Diverse range of our multidisciplinary projects focus on characterising molecular mechanisms which regulate endothelial cell properties and function in health and chronic diseases and development of fully humanised, and thus clinically relevant, in vitro models using these cells and enabling to mimic complex human systems.
This project aims to uncover mechanisms of resistance in kidney cancer. The project utilises state of the art co-culture models to deconvolute resistance mechanisms aiming to develop new treatments for this chronic disease.
This project aims to uncover mechanisms of resistance in melanoma. The project utilises state of the art co-culture models to deconvolute resistance mechanisms aiming to develop new treatments for this chronic disease.
This project aims to uncover the role of endothelial cells in chronic lung disease. The project develops a humanised model focused on accurately representing endothelial heterogeneity and characterising alterations to this heterogeneity in chronic lung disease. This work aims to develop new avenues for therapeutic management for chronic lung diseases.
This project aims to provide novel biological insights in pharmacological properties of human endothelial cells. This project utilises a mass spectrometry-based label-free quantitative proteomics pipeline in conjunction with High Performance Computer VIPER.
This project aims to isolate high purity genomic DNA from pancreatic cyst fluid samples and perform whole genome sequencing analysis of pancreatic cancer samples in comparison to the reference genome, to identify disease-related variants.
publications AND PRE-PRINTS
Novel protein Interaction Network of Human Calcitonin Receptor-like Receptor Revealed by Label-Free Quantitative Proteomics (Pre-Print)
Dimitrios Manolis, Shirin Hasan, Camille Ettelaie, Anthony Maraveyas, Darragh P. O’Brien, Benedikt M. Kessler, Holger Kramer, Leonid L. Nikitenko
Altered Heterogeneity of Ageing Lung Endothelium is a Hallmark of Idiopathic Pulmonary Fibrosis (Pre-Print)
Eamon C. Faulkner, Adam A. Moverley, Simon P. Hart, Leonid L. Nikitenko
MYPT1 is a non-canonical AKAP that tethers PKA to the MLCP signaling node (Pre-Print)
Jawad S Khalil, Paulo A. Saldanha, Connor M Blair, Jiayue Ling, Wei Ji, George S. Baillie, Khalid M Naseem, Leonid L Nikitenko, Francisco Rivero
Complex transcriptional profiles of the PPP1R12A gene in cells of the circulatory system as revealed by in silico analysis and reverse transcription PCR
Paulo A. Saldanha, Olapeju I. Bolan, Timothy M. Palmer, Leonid L. Nikitenko, Francisco Rivero
A Patients Guide to Pulmonary Fibrosis (2nd edition)
Karolina Jagielka, Eamon C. Faulkner, Simon P. Hart, Leonid L. Nikitenko
Low molecular weight heparin and direct oral anticoagulants influence tumour formation, growth, invasion and vascularisation by separate mechanisms
Sophie Featherby, Yu Pei Xiao, Camille Ettelaie, Leonid L. Nikitenko, John Greenman, Anthony Maraveyas
the LONDON PANCREAS WORKSHOP 2023
Endothelial Cell Biology Health *GDP PhD Cluster
Multi disciplinary group of which includes eight fundamental science and clinical academics supporting three PhD students at the University of Hull. The cluster focuses on Human endothelial cells in health and chronic disease through translational research and computational analysis pipelines.
Endothelial Cell Journal Club
The journal club is a student run bi-weekly meeting where we discuss and present relevant papers to keep us up to date on developments in the field and develop our presentation and peer reviewing skills.
The endothelial cell research fund (ECRF) is to support undergraduate and postgraduate students conducting research projects in the field of endothelial cell biology (travel, reagents etc.) and also including invitation of the external speakers for giving talks on endothelial cell research at the Endothelial Cell Journal Club Meetings and the University of Hull Biomed/CAM Seminars.
The account is now open and ready to receive donations. If you wish to support the ECR fund, please find enclosed the links to the online pages for either single gifts or direct debits:
In the Designation section the donor would need to choose "ECR Fund".