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Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 109
Issue DateTitleAuthor(s)
2020Towards an understanding of the genetic aspects of hypoplastic left heart syndrome (HLHS)Al-Qahtani, Ahlam
2020Molecular genetic studies of inherited cystic kidney disease in OmanAl Alawi, Intisar Hamed
2020Optimisation of protocols for ex vivo expansion of limbal stem cells and their enrichmentBojic, Sanja
2019The role of endoglin in endothelial and mesenchymal cells during development, maintenance and repair of the heartSingh, Esha
2019The role of MYO9A at the neuromuscular junctionO'Connor, Emily Ann
2019The role of WT1 in nephron endowment and glomeruloscerosis (GS) / Chronic Kidney Disease (CKD) /Bin Ahmad, Ahzah Hadi
2019Investigating inherited renal disorders and identification of a novel cause of Joubert syndromeAlkanderi, Sumaya
2019Congenital myasthenic syndromes and the therapeutic modulation of the neuromuscular junctionMcMacken, Grace Maria
2019Quantitative magnetic resonance imaging in muscular dystrophiesMurphy, Alexander Peter
2019Clinical significance and regulation of cohesin depletion in mammalian oocytesCooney, Dan
2019Biomarkers of mismatch repair deficiency in colorectal cancer and cancer predisposition syndromesGallon, Richard John
2018Characterisation of MYB and TRKB as candidate targets in CYLD cutaneous syndromeSinclair, Naomi Kathryn
2018a Circulating cell free mitochondrial DNA copy number variation in neurodegenerative diseaseLowes, Hannah
2019Characterisation of a zebrafish model of Wolfram SyndromeCairns, George Edward
2019Studying arrythmogenic right ventricular cardiomyopathy : dysplasia using induced pluripotent stem cellsLee, David Charles
2018Genetic heterogeneity in collagen VI-related myopathyTorabi Farsani, Golara
2018Investigating the role of the extracellular matrix (ECM) on pluripotent stem cell differentiation towards retinal lineagesFelemban, Majed Abdulsamad A
2018Can short sprints during moderate intensity exercise reduce the incidence of exercise mediated hypoglycaemia in individuals with type 1 diabetes?Chetty, Tarini
2018The disease mechanisms of skeletal dysplasia caused by two aggrecan mutationsGibson, Beth Grace
2018A systematic comparison of integrated genomic platforms and bioinformatics pipelines for next generation sequencing in patients with rare neuromuscular diseaseAlrohaif, Hadil E. D. M.
Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 109