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Showing results 21 to 40 of 46 < previous next >

Issue Date	Title	Author(s)
2008	IFNGRI and TNFAIP3 in a Maltese family with a highly penetrant form of osteoporosis	Gatt, Claire
2012	Infliximab, osteoporosis and osteopoenia in Crohn’s disease	Azzopardi, Neville; Ellul, Pierre; Saliba, Christian; LaFerla, Godfrey; Grech, Godfrey
2012	The influence of anti-asthma drugs on the transcriptional regulation of chemokine receptor 3 (CCR3)	Grech, Godfrey; Fenech, Anthony G.; Ellul-Micallef, Roger; Grech, Godwin M.
2010	The influence of MU Opioid receptor polymorphism on ligand mediated signalling	Bajada, Edwina
2010	The influence on the transcriptional regulation of chemokine receptor 3 (CCR3)	Grech, Godwin M.
2012	Investigating the frequency of the G23D mutation causing DHPR deficiency in the Maltese population.	Tabone, Christine
1992	Investigations on the gene for human antithrombin III	Grima, Victoria (1992)
2008	Linkage analysis in a familial case of idiopathic epilepsy and its implications in drug development	Cassar, Maria Louisa
2019	Low-prevalence of NOD2 polymorphisms in a Maltese IBD cohort	Schembri, J.; Pace, Nikolai Paul; Degenhardt, F.; Franke, A.; Ellul, P.
2014	METTL23, a transcriptional partner of GABPA, is essential for human cognition	Reiff, 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.
2017-03-23	Molecular 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 chromosome	Pace, Nikolai Paul; Frideriki, Maggouta; Twigden, Melissa; Borg, Isabella
2014	The Negative Elongation Factor Complex – a poorly understood multi-faceted transcript-processing complex	Baron, Byron
2011	Novel interactions of the GABPα transcription factor complex	Baron, Byron
2010	Osteogenic bioactivity and oestrogen growth factor response induced by extracts from Ceratonia siliqua	Vella, Kevin
2016	Osteoporosis / Osteopoenia in Crohn's disease patients expressing the ATG16L1 gene variants	Azzopardi, Neville
2015	Pharmacogenetic implications in clopidogrel therapy : a pharmacist-Ied management approach	Wirth, Francesca
2012	Pharmacogenomic reactivation of foetal heamoglobin.	Grech, Laura
2019	Phenotypic and genetic markers of disease severity in a Maltese IBD cohort	Schembri, J.; Pace, Nikolai Paul; Piscopo, N.; Degenhardt, F.; Franke, A.; Ellul, P.
2000	A population study of FMR1 mutations in Malta	Said, Edith
2020	Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene	Cooper-Knock, Johnathan; Zhang, Sai; Kenna, Kevin P.; Moll, Tobias; Franklin, John P.; Allen, Samantha; Ghahremani Nezhad, Helia; Iacoangeli, Alfredo; Yacovzada, Nancy Y.; Eitan, Chen; Hornstein, Eran; Elhaik, Eran; Celadova, Petra; Bose, Daniel; Farhan, Sali; Fishilevich, Simon; Lancet, Doron; Morrison, Karen E.; Shaw, Christopher E.; Al-Chalabi, Ammar; Veldink, Jan H.; Kirby, Janine; Snyder, Michael P.; Shaw, Pamela J.; Cauchi, Ruben J.; Project MinE ALS Sequencing Consortium

Showing results 21 to 40 of 46 < previous next >