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Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 119
Issue DateTitleAuthor(s)
2020Tissue engineering approaches to study biomechanical sensing in pseudoachondroplasiaDe Las Heras Ruiz, Thais
2021Use of Serial Block Face-Scanning Electron Microscopy to Study the Ultrastructure of Vertebrate and Invertebrate BiologyCocks, Erin Twynham
2019Improving our understanding of autosomal dominant Retinitis Pigmentosa using PRPF31 patient-specific induced pluripotent stem cells (iPSCs)Goes Barbosa Buskin, Adriana
2020The Role of Non-Classical Monocytes and the CX3CL1/CX3CR1 Axis in the Immune Response to Myocardial Ischemia-ReperfusionMarsh, Sarah Alice
2020A Col9a3 exon 3 skipping mouse as a novel model for multiple epiphyseal dysplasiaLecci, Syliva
2020Genetic risk factors and disease mechanisms in mitochondrial optic neuropathyNesbitt, Sarah Elizabeth
2020Investigating the regulation of alternative splicing by Tra2 proteins and RBMX in triple negative breast cancer cellsHysenaj, Gerald
2020Investigating gene regulatory networks in aorti arch artery developmentStothard, Catherine Anne
2020Identification and characterisation of novel mechanisms affecting prostate cancer cell growthLivermore, Karen Elizabeth
2020Senescence as a potential therapeutic target for ischaemia-reperfusion injury following acute myocardial infarctionDookun, Emily
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
Collection's Items (Sorted by Submit Date in Descending order): 1 to 20 of 119