Browsing "Institute of Genetic Medicine" by Title

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Issue DateTitleAuthor(s)
2017The activation and disarming of Protease-activated receptor 2Falconer, Adrian.
2014Ageing in the zebrafish heartBurns, David
2014Analyses of Pax9 functions in the developing and adult mouse mammary glandWang, Liming
2013Analysis and interpretation of next-generation sequencing data for the identification of genetic variants involved in cardiovascular malformationHouniet, Darren Theo
2014Analysis of RNA binding proteins using stable cell linesKheirollahi Kouhestani, Mahsa
2019Biomarkers of mismatch repair deficiency in colorectal cancer and cancer predisposition syndromesGallon, Richard John
2018Can short sprints during moderate intensity exercise reduce the incidence of exercise mediated hypoglycaemia in individuals with type 1 diabetes?Chetty, Tarini
2015Catheter ablation in patients with atrial fibrillation : mapping refinements, outcome prediction and effect on quality of lifeRaine, Daniel Thomas
2019Characterisation of a zebrafish model of Wolfram SyndromeCairns, George Edward
2014Characterisation of cardiosphere derived cells :investigating hypoxic pre-conditioning on pro-angiogenic properties and tracking the cardiac fibroblast componentAmirrasouli, Muhammad Mehdi
2015Characterisation of limbal stem cellsShaharuddin, Bakiah Binti
2018Characterisation of MYB and TRKB as candidate targets in CYLD cutaneous syndromeSinclair, Naomi Kathryn
2018Characterisation of the epigenome of an in vitro model of chondrogenesisCheung, Kathleen
2018a Circulating cell free mitochondrial DNA copy number variation in neurodegenerative diseaseLowes, Hannah
2017Clinical and genetic characterisation of hereditary motor neuropathiesBansagi, Boglarka Krisztina
2014The clinical and genetic characteristics of congenital myasthenic syndromesChaouch, Amina
2011Clinical and histological implications of genotyping in Crohn’s diseaseHanson, Catherine Elisabeth
2019Clinical significance and regulation of cohesin depletion in mammalian oocytesCooney, Dan
2020A Col9a3 exon 3 skipping mouse as a novel model for multiple epiphyseal dysplasiaLecci, Syliva
2016Complement abnormalities in membranoproliferative glomerulonephritis and C3 glomerulopathyWong, Edwin Kwan Soon