Collection's Items (Sorted by Submit Date in Descending order): 41 to 60 of 120
| Issue Date | Title | Author(s) |
| 2017 | Modelling severe paediatric aplastic anaemia using induced pluripotent stem cell technology | Melguizo Sanchis, Dario |
| 2017 | Genetic factors modulating mitochondrial DNA copy number | Brennan, Rebecca Ruth |
| 2017 | Clinical and genetic characterisation of hereditary motor neuropathies | Bansagi, Boglarka Krisztina |
| 2017 | The role of mechanical and chemical cues on corneal cells function | Zainal Abidin, Fadhilah Binti |
| 2017 | Exploring outcome measures for adults with myotonic dystrophy type 1 | Jimenez Moreno, Aura Cecilia |
| 2017 | Investigating the brain in mouse models of Duchenne muscular dystrophy | Bagdatlioglu, Emine |
| 2017 | The relationship between the cellular composition of the aortic adventitia and atherosclerosis | Curley, Natash |
| 2017 | A GFPT1 deficient mouse model of congenital myasthenic syndrome | Issop, Yasmin |
| 2017 | Pathophysiology of anoctaminopathy (LGMD2L) | Kirk, Calum Norman Robert |
| 2017 | Investigating the role of Rac1 in cardiovascular development | Dodds, Rebecca |
| 2017 | Investigating the potential role of recombination regulator PRDM9 in mitochondria / | McIlwaine, Emily |
| 2017 | Investigating the reversibility and tissue specificity of mitochondrial disorders | Bartsakoulia, Marina |
| 2017 | The activation and disarming of Protease-activated receptor 2 | Falconer, Adrian. |
| 2017 | Mechanisms and impact of Post-transcriptional Exon Shuffling (PTES) | Izuogu, Ginikachukwu Osagie |
| 2017 | Exosomal protein deficiencies : how abnormal RNA metabolism results in childhood-onset neurological diseases | Giunta, Michele |
| 2017 | Msx1 modulates the Pax9-null cardiovascular phenotype | Khasawneh, Ramada Rateb Abdel Karim |
| 2017 | Timing and regulation of cohesion depletion during mammalian oogenesis | Ballesteros Mejia, Randy Carlos |
| 2017 | The effect of pronuclear transfer on human preimplantation development | Richardson, Jessica Louise |
| 2017 | Investigating retinal pathology in patients carrying m.3243A>G mutation using human induced pluripotent stem cells | Chichagova, Valeria |
| 2016 | Diagnosing "his" infertility : men's experiences and reflections on the diagnosis of azoospermia | Karavolos, Stamatios |
Collection's Items (Sorted by Submit Date in Descending order): 41 to 60 of 120
