‘ESDN’, ‘EuroGrow’ & ‘SYBIL’ – 15+ years of EU network approaches for diagnosis and research of rare skeletal diseases Sheffield Abstract.
ESCEO13-IOF Congress in Rome, Italy, April 17-20
“How do rare genetic diseases contribute to the understanding of common bone diseases? – The contribution of chondrodysplasias to the understanding of osteoarthritis” Proposed programme ECCEO13 – PRECLINICAL SYMPO.
VI International Congress on Stress Proteins in Biology and Medicine in Sheffield, UK, August 18-22
“ARMET/MANF and CRELD2 are components of an ER stress response provoked by inappropriate formation of disulphide bonds: implications for genetic skeletal diseases”
ISDS 11th Biennial Meeting in Bologna, Italy, August 28-31
“Pseudoachondroplasia and multiple epiphyseal dysplasia; key disease triggers in representative genotypes” ISDS 2013 Abstract.
BSMB in Cardiff, UK, September 2-3
“Preliminary characterisation of Creld2 null mice suggest a possible role in cartilage development” BSMB Poster 2013.
Pan Pacific Connective Tissue Societies Symposium in Hong Kong, China, November 24-27
“A V156D matrilin-1 mouse model reveals limited intracellular retention of mutant protein that does not lead to short-limbed dwarfism” PPCTSS 2013 poster.
“Lessons from Rare Diseases of Cartilage” in Liverpool, UK, October 16.
“Disease mechanisms in chondrodysplasias” Liverpool 2013.