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Issue DateTitleAuthor(s)
2021Apc-mutant cells act as supercompetitors in intestinal tumour initiationNeerven, Sanne M. van; Groot, Nina E. de; Nijman, Lisanne E.; Scicluna, Brendon P.; Driel, Milou S. van; Lecca, Maria C.; Warmerdam, Daniël O.; Kakkar, Vaishali; Moreno, Leandro F.; Vieira Braga, Felipe A.; Sanches, Delano R.; Ramesh, Prashanthi; Ten Hoorn, Sanne; Aelvoet, Arthur S.; Boxel, Marouska F. van; Koens, Lianne; Krawczyk, Przemek M.; Koster, Jan; Dekker, Evelien; Medema, Jan Paul; Winton, Douglas J.; Bijlsma, Maarten F.; Morrissey, Edward; Léveillé, Nicolas; Vermeulen, Louis
2020Association between Vitamin D receptor polymorphisms and Systemic Lupus Erythematosus in a Maltese cohortGrech Meli, Jordan
2008Cognition in sepiapterin reductase deficiencyBalani, Sunaina
2012The effect of modifier genes on foetal haemoglobin in the Maltese population.Scerri, Gary
2012The effects of trans-regulatory loci on globin gene controlDaw, Amal Mohammed
2007Extended haplotype of the CTLA-4 Gene within the coeliac patients in the Maltese population.Muscat, Karen
2011From genome to epigenome : Ethical implications of epigenetic researchTanti, Robert (2011)
1995Genes as the common heritage of mankind : ethical issues in patenting lifeAgius, Emmanuel
2013Genetic analysis of olive (Olea europea L.) varietes in the Maltese islands using DNA markers: method development and technique evaluationMazzitelli, Oriana
2007The genetics of osteoporosisVidal, Christopher
2007Genome organisationBlundell, Renald
2008IFNGRI and TNFAIP3 in a Maltese family with a highly penetrant form of osteoporosisGatt, Claire
2010The influence of MU Opioid receptor polymorphism on ligand mediated signallingBajada, Edwina
2010The influence on the transcriptional regulation of chemokine receptor 3 (CCR3)Grech, Godwin M.
2012Investigating the frequency of the G23D mutation causing DHPR deficiency in the Maltese population.Tabone, Christine
1992Investigations on the gene for human antithrombin IIIGrima, Victoria (1992)
2008Linkage analysis in a familial case of idiopathic epilepsy and its implications in drug developmentCassar, Maria Louisa
2019Low-prevalence of NOD2 polymorphisms in a Maltese IBD cohortSchembri, J.; Pace, Nikolai Paul; Degenhardt, F.; Franke, A.; Ellul, P.
2014METTL23, a transcriptional partner of GABPA, is essential for human cognitionReiff, Rachel E.; Ali, Bassam R.; Baron, Byron; W. Yu, Timothy; Ben-Salem, Salma; E. Coulter, Michael; Schubert, Christian R.; Hill, R. Sean; Akawi, Nadia A.; Al-Younes, Banan; Kaya, Namik; Evrony, Gilad D.; Al-Saffar, Muna; Felie, Jillian M.; Partlow, Jennifer N.; Sunu, Christine M.; Schembri-Wismayer, Pierre; Alkuraya, Fowzan S.; Meyer, Brian F.; Walsh, Christopher A.; Al-Gazali, Lihadh; Mochida, Ganeshwaran H.
2017-03-23Molecular cytogenetic characterisation of a novel de novo ring chromosome 6 involving a terminal 6p deletion and terminal 6q duplication in the different arms of the same chromosomePace, Nikolai Paul; Frideriki, Maggouta; Twigden, Melissa; Borg, Isabella