Literature DB >> 6772982

Ovine ceroid-lipofuscinosis: a model of Batten's disease.

R D Jolly, A Janmaat, D M West, I Morrison.   

Abstract

An inherited neurological disease of sheep was characterized by the intracellular accumulation of autofluorescent lipopigments in neurones and a wide variety of other cells within the body. The staining, fluorescent, ultrastructural and physical characteristics of the storage material were similar to those found in a heterogeneous group of storage diseases of children known as Batten's disease or the ceroid-lipofuscinoses. The ovine disease did not exactly fit any of the main human entities, but had features in common with both the late infantile and juvenile forms. It was concluded that this was a useful model for studying the pathogenesis of this type of storage disease and for therapeutic trials. A flock of sheep is maintained for this purpose.

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Year:  1980        PMID: 6772982     DOI: 10.1111/j.1365-2990.1980.tb00290.x

Source DB:  PubMed          Journal:  Neuropathol Appl Neurobiol        ISSN: 0305-1846            Impact factor:   8.090


  17 in total

1.  Neurovisceral ceroid-lipofuscinosis in blind Devon cattle.

Authors:  P A Harper; K H Walker; P J Healy; W J Hartley; A J Gibson; J S Smith
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

2.  Quantitative analysis of retinal outer segments in ovine ceroid-lipofuscinosis.

Authors:  D Armstrong; R Jolly
Journal:  Vet Res Commun       Date:  1986-01       Impact factor: 2.459

3.  Neuronal ceroidosis (ceroid-lipofuscinosis) in a Blue Heeler dog.

Authors:  D Y Cho; H W Leipold; R Rudolph
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

Review 4.  Hereditary ceroid-lipofuscinosis: methylated amino acids in storage body proteins.

Authors:  M L Katz
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

5.  Autofluorescence emission spectra of neuronal lipopigment in animal and human ceroidoses (ceroid-lipofuscinoses).

Authors:  J H Dowson; D Armstrong; N Koppang; B D Lake; R D Jolly
Journal:  Acta Neuropathol       Date:  1982       Impact factor: 17.088

6.  Amacrine and horizontal cell dysfunction in adult ceroid-lipofuscinosis (Kufs disease) and anatomical correlates in the ovine model.

Authors:  D Armstrong; M Benedetto; D Samuelson
Journal:  Int Ophthalmol       Date:  1985-04       Impact factor: 2.031

7.  Characterization of the expressed genes for subunit c of mitochondrial ATP synthase in sheep with ceroid lipofuscinosis.

Authors:  S M Medd; J E Walker; R D Jolly
Journal:  Biochem J       Date:  1993-07-01       Impact factor: 3.857

8.  Mitochondrial ATP synthase subunit c stored in hereditary ceroid-lipofuscinosis contains trimethyl-lysine.

Authors:  M L Katz; C L Gao; J A Tompkins; R T Bronson; D T Chin
Journal:  Biochem J       Date:  1995-09-15       Impact factor: 3.857

9.  Juvenile ceroid lipofuscinosis. Evidence for methylated lysine in neural storage body protein.

Authors:  M L Katz; M Rodrigues
Journal:  Am J Pathol       Date:  1991-02       Impact factor: 4.307

10.  Manifestation of neuronal ceroid lipofuscinosis in Australian Merino sheep: observations on altered behaviour and growth.

Authors:  Greg M Cronin; Danai F Beganovic; Amanda L Sutton; DavidJ Palmer; Peter C Thomson; Imke Tammen
Journal:  Appl Anim Behav Sci       Date:  2016-02-01       Impact factor: 2.448

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