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Neurobiology of Disease|February 18, 2006
Selectively increased sensitivity of cerebellar granule cells to AMPA receptor-mediated excitotoxicity in a mouse model of Batten diseaseAttila D Kovács, Jill M Weimer, David A PearceExpert Opinion on Medical Diagnostics|March 16, 2013
Diagnosis of neuronal ceroid lipofuscinosis: mutation detection strategiesAmanda L Getty, Paul G Rothberg, David A PearceHuman Molecular Genetics|March 30, 2013
The role of nonsense-mediated decay in neuronal ceroid lipofuscinosisJake N Miller, Chun-Hung Chan, David A PearceHuman Molecular Genetics|March 8, 2007
Absence of Btn1p in the yeast model for juvenile Batten disease may cause arginine to become toxic to yeast cellsSeasson Phillips Vitiello, Devin M Wolfe, David A PearceHuman Molecular Genetics|August 6, 2008
Transcript and in silico analysis of CLN3 in juvenile neuronal ceroid lipofuscinosis and associated mouse modelsChun-Hung Chan, Hannah M Mitchison, David A PearceHuman Molecular Genetics|September 11, 2014
The novel Cln1(R151X) mouse model of infantile neuronal ceroid lipofuscinosis (INCL) for testing nonsense suppression therapyJake N Miller, Attila D Kovács, David A PearceJournal of Child Neurology|July 24, 2013
A novel c.1135_1138delCTGT mutation in CLN3 leads to juvenile neuronal ceroid lipofuscinosisArlene V Drack, Jake N Miller, David A PearceJournal of Child Neurology|July 11, 2013
Seizure susceptibility, phenotype, and resultant growth delay in the nclf and mnd mouse models of neuronal ceroid lipofuscinosesElizabeth Kriscenski-Perry, Attila D Kovács, David A PearceInvestigative Ophthalmology & Visual Science|August 27, 2003
Optic nerve degeneration in a murine model of juvenile ceroid lipofuscinosisRebecca M Sappington, David A Pearce, David J CalkinsJournal of Neuroscience Research|July 20, 2007
Progressive oxidative damage in the central nervous system of a murine model for juvenile Batten diseaseJared W Benedict, Crosby A Sommers, David A PearcePageof 18