294 results on '"Jolly, R. D."'
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2. Mucopolysaccharidosis type VI in a Miniature Poodle-type dog caused by a deletion in the arylsulphatase B gene
3. Lysosomal storage of a mitochondrial protein in Batten’s disease (ceroid lipofuscinosis)
4. Intracisternal enzyme replacement therapy in lysosomal storage diseases: dispersal pathways, regional enzyme concentrations and the effect of posttreatment posture
5. Intracisternal enzyme replacement therapy in lysosomal storage diseases: routes of absorption into brain
6. Accumulation of sphingolipid activator proteins (SAPs) A and D in granular osmiophilic deposits in miniature Schnauzer dogs with ceroid-lipofuscinosis
7. Batten disease (ceroid-lipofuscinosis): The enigma of subunit c of mitochondrial ATP synthase accumulation
8. Ceroid, lipofuscin and the ceroid-lipofuscinoses (Batten Disease)
9. Bovine ceroid-lipofuscinosis (Batten's disease): The major component stored is the DCCD-reactive proteolipid, subunit c, of mitochondrial ATP synthase
10. Lipopigments in Veterinary Pathology: Pathogenesis and Terminology
11. Glycoconjugates in Storage Cytosomes from Ceroid-Lipofuscinosis (Batten’s Disease) and in Lipofuscin from Old-Age Brain
12. Lysosomal Storage of the DCCD Reactive Proteolipid Subunit of Mitochondrial ATP Synthase in Human and Ovine Ceroid Lipofuscinoses
13. Familial episodic ataxia in lambs is potentially associated with a mutation in the fibroblast growth factor 14 (FGF14) gene
14. Round-table discussion of animal models of ceroid-lipofuscinosis (Batten Disease)
15. Autofluorescence emission spectra of neuronal lipopigment in animal and human ceroidoses (ceroid-lipofuscinoses)
16. The subependymal plate and associated ependyma in the dog. An ultrastructural study
17. Pathology of Mucopolysaccharidosis IIIA in Huntaway Dogs
18. Histological diagnosis of mucopolysaccharidosis IIIA in a wire-haired dachshund
19. Ovine neuronal ceroid lipofuscinosis: a large animal model syntenic with the human neuronal ceroid lipofuscinosis variant CLN6.
20. Lysosomal Storage Diseases of Animals: An Essay in Comparative Pathology
21. Comparative biology of the neuronal ceroid‐lipofuscinoses (NCL): An overview
22. The neuronal ceroid-Iipofuscinoses (Batten disease): comparative aspects
23. Canine ceroid-lipofuscinoses: A review and classification
24. Characterization of the expressed genes for subunit c of mitochondrial ATP synthase in sheep with ceroid lipofuscinosis
25. The sequence of the major protein stored in ovine ceroid lipofuscinosis is identical with that of the dicyclohexylcarbodiimide-reactive proteolipid of mitochondrial ATP synthase
26. Congenital brain oedema of Hereford calves.
27. Carcinoma of the small intestine in sheep.
28. Different Patterns of Hydrophobic Protein Storage in Different Forms of Neuronal Ceroid Lipofuscinosis (NCL, Batten Disease).
29. CEROID-LIPOFUSCINOSIS (BATTEN'S DISEASE): PATHOGENESIS AND SEQUENTIAL NEUROPATHOLOGICAL CHANGES IN THE OVINE MODEL.
30. STRINGHALT IN HORSES: A DISTAL AXONOPATHY.
31. CEROID-LIPOFUSCINOSIS (BATTEN'S DISEASE): PATHOGENESIS OF BLINDNESS IN THE OVINE MODEL.
32. OVINE CEROID-LIPOFUSCINOSIS: A MODEL OF BATTEN'S DISEASE.
33. LYSOSOMAL STORAGE DISEASES.
34. Lipofuscin in bovine muscle and brain: a model for studying age pigment.
35. Mannosidosis: Ocular lesions in the bovine model.
36. The pathology of an inherited cataract of sheep.
37. Persistent lymphocytosis and virus-like particles in lymphocytes of sheep inoculated with cell-free extracts derived from ovine malignant lymphomas.
38. Mannosidosis-pathogenesis of lesions in exocrine cells.
39. STORAGE DISEASES OF DOMESTIC ANIMALS.
40. Some Observations on Surface Lipids of Virulent and Attenuated Strains of Corynebacterium ovis.
41. The pathology of the central nervous system in pseudolipidosis of Angus calves.
42. Mitochondrial dysfunction in the neuronal ceroid-lipofuscinoses (Batten disease)
43. Progressive myelopathy and neuropathy in New Zealand Huntaway dogs
44. β-Mannosidosis in a Salem calf: A new storage disease of cattle
45. Bovine ceroid-lipofuscinosis: Pathology of blindness
46. The catabolism of mammalian glycoproteins. Comparison of the storage products in bovine, feline and human mannosidosis
47. Enzyme Replacement Therapy—An Experiment of Nature in a Chimeric Mannosidosis Calf
48. The nature of the residual α-mannosidase in plasma in bovine mannosidosis
49. Mannosidosis in Angus cattle. The enzymic defect
50. Ceroid lipofuscinosis in sheep. II. The major component of the lipopigment in liver, kidney, pancreas, and brain is low molecular weight protein.
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