Literature DB >> 20978939

Gaucher disease in sheep.

Litsa Karageorgos1, Malcolm J Lancaster, Judith S Nimmo, John J Hopwood.   

Abstract

Gaucher disease, an autosomal recessive lysosomal storage disorder caused by mutations in the β-glucocerebrosidase gene, was recently discovered in sheep on a "Southdown" sheep stud in Victoria, Australia. Clinical signs include neuropathy, thickened leathery skin, and ichthyosis, with lambs unable to stand from birth. Affected lambs were found to be deficient in glucocerebrosidase activity, and mutational analysis found them to be homozygous for the missense mutations c.1142G>A (p.C381Y) and c.1400C>T (p.P467L). In addition, four silent mutations were detected (c.777C>A [p.Y259Y], c1203A>G [p.Q401Q], c.1335T>C [p.I445I], c.1464C>G [p.L488L]). The human equivalent [C342Y] to the C381Y mutation leads to an acute neuronopathic phenotype in patients. Identification of an acute neuronopathic form of Gaucher disease in sheep provides a large animal model that will enable studies of pathology and evaluation of therapies to treat this common lysosomal storage disorder.

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Year:  2010        PMID: 20978939     DOI: 10.1007/s10545-010-9230-3

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  16 in total

1.  Identification of two novel mutations, L105R and C342R, in Type I Gaucher disease.

Authors:  F Y M Choy; A Vaags; K Wong; D Macgregor; B Fernandez; C Prasad
Journal:  Clin Genet       Date:  2002-03       Impact factor: 4.438

Review 2.  Hematologically important mutations: Gaucher disease.

Authors:  Ernest Beutler; Terri Gelbart; C Ronald Scott
Journal:  Blood Cells Mol Dis       Date:  2005-09-26       Impact factor: 3.039

3.  Correlation among genotype, phenotype, and biochemical markers in Gaucher disease: implications for the prediction of disease severity.

Authors:  Phillip D Whitfield; Paul Nelson; Peter C Sharp; Colleen A Bindloss; Caroline Dean; Elaine M Ravenscroft; Beverley A Fong; Michael J Fietz; John J Hopwood; Peter J Meikle
Journal:  Mol Genet Metab       Date:  2002-01       Impact factor: 4.797

4.  Neurovisceral glucocerebroside storage (Gaucher's disease) in a dog.

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Journal:  Vet Pathol       Date:  1973       Impact factor: 2.221

5.  Histiocytosis in two pigs and a cow: conditions resembling lipid storage disorders in man.

Authors:  A T Sandison; L J Anderson
Journal:  J Pathol       Date:  1970-03       Impact factor: 7.996

6.  The human glucocerebrosidase gene and pseudogene: structure and evolution.

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Journal:  Genomics       Date:  1989-01       Impact factor: 5.736

7.  Epidermal abnormalities may distinguish type 2 from type 1 and type 3 of Gaucher disease.

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Journal:  Pediatr Res       Date:  1996-01       Impact factor: 3.756

8.  Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies.

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Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

Review 9.  Gaucher disease: mutation and polymorphism spectrum in the glucocerebrosidase gene (GBA).

Authors:  Kathleen S Hruska; Mary E LaMarca; C Ronald Scott; Ellen Sidransky
Journal:  Hum Mutat       Date:  2008-05       Impact factor: 4.878

10.  Gaucher's disease: a case history with extensive lipid storage in the brain.

Authors:  R W Leech; R M Shuman; W D Putnam; F Rance; T T Jewett
Journal:  Am J Clin Pathol       Date:  1985-04       Impact factor: 2.493

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Journal:  Transgenic Res       Date:  2016-01-28       Impact factor: 2.788

Review 2.  Identification and characterization of pharmacological chaperones to correct enzyme deficiencies in lysosomal storage disorders.

Authors:  Kenneth J Valenzano; Richie Khanna; Allan C Powe; Robert Boyd; Gary Lee; John J Flanagan; Elfrida R Benjamin
Journal:  Assay Drug Dev Technol       Date:  2011-06       Impact factor: 1.738

3.  Engineering Large Animal Species to Model Human Diseases.

Authors:  Christopher S Rogers
Journal:  Curr Protoc Hum Genet       Date:  2016-07-01

Review 4.  Animal models for Gaucher disease research.

Authors:  Tamar Farfel-Becker; Einat B Vitner; Anthony H Futerman
Journal:  Dis Model Mech       Date:  2011-10-04       Impact factor: 5.758

5.  Rapid and Progressive Regional Brain Atrophy in CLN6 Batten Disease Affected Sheep Measured with Longitudinal Magnetic Resonance Imaging.

Authors:  Stephen J Sawiak; Sunthara Rajan Perumal; Skye R Rudiger; Loren Matthews; Nadia L Mitchell; Clive J McLaughlan; C Simon Bawden; David N Palmer; Timothy Kuchel; A Jennifer Morton
Journal:  PLoS One       Date:  2015-07-10       Impact factor: 3.240

Review 6.  The Translational Benefits of Sheep as Large Animal Models of Human Neurological Disorders.

Authors:  Samantha J Murray; Nadia L Mitchell
Journal:  Front Vet Sci       Date:  2022-02-15

7.  Ex vivo susceptibility-weighted imaging anatomy of canine brain-comparison of imaging and histological sections.

Authors:  Germain Arribarat; Benjamin Cartiaux; Samuel Boucher; Charles Montel; Hélène Gros-Dagnac; Yoann Fave; Patrice Péran; Giovanni Mogicato; Alexandra Deviers
Journal:  Front Neuroanat       Date:  2022-09-02       Impact factor: 3.543

8.  Volumetric assessment and longitudinal changes of subcortical structures in formalinized Beagle brains.

Authors:  Francesca Del Signore; Germain Arribarat; Leonardo Della Salda; Giovanni Mogicato; Alexandra Deviers; Benjamin Cartiaux; Massimo Vignoli; Patrice Peran; Francesco de Pasquale
Journal:  PLoS One       Date:  2022-10-07       Impact factor: 3.752

Review 9.  Large animal models of rare genetic disorders: sheep as phenotypically relevant models of human genetic disease.

Authors:  Ashish R Pinnapureddy; Cherie Stayner; John McEwan; Olivia Baddeley; John Forman; Michael R Eccles
Journal:  Orphanet J Rare Dis       Date:  2015-09-02       Impact factor: 4.123

  9 in total

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