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European Journal of Biochemistry|August 5, 2004
Neuroserpin Portland (Ser52Arg) is trapped as an inactive intermediate that rapidly forms polymers: implications for the epilepsy seen in the dementia FENIBDidier Belorgey, Lynda K Sharp, Damian C Crowther, et al.
Experimental and Molecular Pathology|February 9, 2012
Prion-induced toxicity in PrP transgenic DrosophilaAlana M Thackray, Farooq Muhammad, Chang Zhang, et al.
European Journal of Human Genetics : EJHG|December 25, 2003
Practical genetics: alpha-1-antitrypsin deficiency and the serpinopathiesDamian C Crowther, Didier Belorgey, Elena Miranda, et al.
Free Radical Biology & Medicine|April 21, 2016
Expression of the alternative oxidase mitigates beta-amyloid production and toxicity in model systemsRiyad El-Khoury, Eveliina Kaulio, Katariina A Lassila, et al.
Biochemistry|March 8, 2014
Retro-inversal of intracellular selected β-amyloid-interacting peptides: implications for a novel Alzheimer's disease treatmentNicola Acerra, Neil M Kad, Douglas A Griffith, et al.
Human Molecular Genetics|February 13, 2008
The intracellular accumulation of polymeric neuroserpin explains the severity of the dementia FENIBElena Miranda, Ian MacLeod, Mark J Davies, et al.
Integrative Biology : Quantitative Biosciences From Nano to Macro|June 24, 2011
The iFly tracking system for an automated locomotor and behavioural analysis of Drosophila melanogasterKai J Kohlhoff, Thomas R Jahn, David A Lomas, et al.
The Journal of Biological Chemistry|June 25, 2009
Endoplasmic reticulum-associated degradation (ERAD) and autophagy cooperate to degrade polymerogenic mutant serpinsHeike Kroeger, Elena Miranda, Ian MacLeod, et al.
The Lancet. Neurology|December 15, 2012
Endoplasmic reticulum dysfunction in neurological diseaseBenoit D Roussel, Antonina J Kruppa, Elena Miranda, et al.
Methods in Enzymology|June 21, 2011
Modeling serpin conformational diseases in Drosophila melanogasterThomas R Jahn, Elke Malzer, John Roote, et al.
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