|
Jolly, R D; Brown, S; Das, A M et al. (2002) Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease). Neurochem Int 40:565-71
|
|
Hughes, S M; Moroni-Rawson, P; Jolly, R D et al. (2001) Submitochondrial distribution and delayed proteolysis of subunit c of the H+-transporting ATP-synthase in ovine ceroid-lipofuscinosis. Electrophoresis 22:1785-94
|
|
Broom, M F; Zhou, C; Broom, J E et al. (1998) Ovine neuronal ceroid lipofuscinosis: a large animal model syntenic with the human neuronal ceroid lipofuscinosis variant CLN6. J Med Genet 35:717-21
|
|
Jolly, R D (1997) The ovine model of neuronal ceroid lipofuscinosis (NCL): its contribution to understanding the pathogenesis of Batten disease. Neuropediatrics 28:60-2
|
|
Palmer, D N; Jolly, R D; van Mil, H C et al. (1997) Different patterns of hydrophobic protein storage in different forms of neuronal ceroid lipofuscinosis (NCL, Batten disease). Neuropediatrics 28:45-8
|
|
Jolly, R D; Walkley, S U (1997) Lysosomal storage diseases of animals: an essay in comparative pathology. Vet Pathol 34:527-48
|
|
Palmer, D N; Tyynela, J; van Mil, H C et al. (1997) Accumulation of sphingolipid activator proteins (SAPs) A and D in granular osmiophilic deposits in miniature Schnauzer dogs with ceroid-lipofuscinosis. J Inherit Metab Dis 20:74-84
|
|
Palmer, D N; Bayliss, S L; Westlake, V J (1995) Batten disease and the ATP synthase subunit c turnover pathway: raising antibodies to subunit c. Am J Med Genet 57:260-5
|
|
Jolly, R D; Palmer, D N (1995) The neuronal ceroid-lipofuscinoses (Batten disease): comparative aspects. Neuropathol Appl Neurobiol 21:50-60
|
|
Moroni-Rawson, P; Palmer, D N; Jolly, R D et al. (1995) Variant proteins in ovine ceroid-lipofuscinosis. Am J Med Genet 57:279-84
|
Showing the most recent 10 out of 43 publications
