Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease.
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Characterization of a human core-specific lysosomal {alpha}1,6-mannosidase involved in N-glycan catabolism.The substrate-specificity of human lysosomal alpha-D-mannosidase in relation to genetic alpha-mannosidosisCerebellar alterations and gait defects as therapeutic outcome measures for enzyme replacement therapy in α-mannosidosis.Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.Mucopolysaccharidoses and mucolipidoses.Molecular definition of bovine argininosuccinate synthetase deficiency.Spectrum of mutations in alpha-mannosidosis.Glycopeptide storage in skin fibroblasts cultured from a patient with alpha-mannosidase deficiency.Mannosidosis: assignment of the lysosomal alpha-mannosidase B gene to chromosome 19 in man.Animal model of human disease: mannosidosis of children, other inherited lysosomal storage diseases.A review of gene therapy in canine and feline models of lysosomal storage disorders.Large animal models of neurological disorders for gene therapy.A canine model of human alpha-L-iduronidase deficiency.The nature of the residual alpha-mannosidase in plasma in bovine mannosidosis.Identification of 83 novel alpha-mannosidosis-associated sequence variants: functional analysis of MAN2B1 missense mutations.Human α-mannosidase produced in transgenic tobacco plants is processed in human α-mannosidosis cell lines.Neurochemistry of the mucopolysaccharidoses: brain lipids and lysosomal enzymes in patients with four types of mucopolysaccharidosis and in normal controls.Evidence that the mutant enzyme in fibroblasts of a patient with mannosidosis does not crossreact with antiserum raised against normal acidic alpha-D-mannosidase.Neurochemistry of the mucopolysaccharidoses: brain glycosaminoglycans in normals and four types of mucopolysaccharidoses.Mannosidosis and its control in Angus and Murray Grey cattle.Mannosidosis in Angus cattle. The enzymic defect.Lysosomal storage diseases of animals: an essay in comparative pathology.Uptake of iodinated human kidney alpha-D-mannosidase by rat liver- Association with membrane elements and stability in vivo and in vitro.A serological investigation into the acidic alpha-D-mannosidase in normal Angus cattle and in a calf with mannosidosis.Purification and properties of alpha-D-mannosidase from the germinated seeds of Medicago sativa (alfalfa).Purification of bovine lysosomal alpha-mannosidase, characterization of its gene and determination of two mutations that cause alpha-mannosidosis.Purification of feline lysosomal alpha-mannosidase, determination of its cDNA sequence and identification of a mutation causing alpha-mannosidosis in Persian cats.Biochemical studies on a case of feline mannosidosis.Immunological characterization of human liver alpha-D-mannosidase.Characterization of human liver alpha-D-mannosidase purified by affinity chromatography.Characterization of the mutant alpha-mannosidase in bovine mannosidosis.Heterozygotes for mannosidosis in Angus and Murray Grey cattle.A urinary pentasaccharide in bovine mannosidosis.Mitogenic effect of alpha-mannosidase on lymphocytes.Mannosidosis in Galloway calves.Functional analysis of an alpha-1,2-mannosidase from Magnaporthe oryzae.Characterization of alpha-mannosidase in feline mannosidosis.The pathology of bovine mannosidosis.Lesions in bovine progressive degenerative myeloencephalopathy ("Weaver") of Brown Swiss cattle.Mannosidosis in Angus cattle: partial characterization of two mannose containing oligosaccharides.
P2860
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P2860
Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease.
description
1972 nî lūn-bûn
@nan
1972年の論文
@ja
1972年論文
@yue
1972年論文
@zh-hant
1972年論文
@zh-hk
1972年論文
@zh-mo
1972年論文
@zh-tw
1972年论文
@wuu
1972年论文
@zh
1972年论文
@zh-cn
name
Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease.
@en
type
label
Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease.
@en
prefLabel
Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease.
@en
P2093
P2860
P356
P1433
P1476
Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease.
@en
P2093
P2860
P356
10.1042/BJ1280069
P407
P577
1972-06-01T00:00:00Z