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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-mannosidosisHigh resolution MRI anatomy of the cat brain at 3 Tesla.Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.Spectrum of mutations in alpha-mannosidosis.A review of gene therapy in canine and feline models of lysosomal storage disorders.Structural analysis of the major urinary oligosaccharides in feline alpha-mannosidosis.Large animal models of neurological disorders for gene therapy.In utero transplantation of monocytic cells in cats with alpha-mannosidosis.Ectopic dendrites occur only on cortical pyramidal cells containing elevated GM2 ganglioside in alpha-mannosidosis.A canine model of human alpha-L-iduronidase deficiency.Linkage mapping of the bovine lysosomal alpha-mannosidase (MANB) gene.Identification of 83 novel alpha-mannosidosis-associated sequence variants: functional analysis of MAN2B1 missense mutations.Effects of swainsonine on rat liver and kidney: biochemical and morphological studiesLysosomal storage diseases of animals: an essay in comparative pathology.Skeletal-muscle alpha-glucosidases in bovine generalized glycogenosis type II.Substrate specificity of the bovine and feline neutral alpha-mannosidasesGM1 gangliosidosis (type 1) in a cat.Inhibition of alpha-L-fucosidase by derivatives of deoxyfuconojirimycin and deoxymannojirimycin.Glycoprotein metabolism in normal and beta-mannosidase-deficient cultured goat skin fibroblasts.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.The enzymic defect and storage products in canine fucosidosisThe catabolism of mammalian glycoproteins. Comparison of the storage products in bovine, feline and human mannosidosis.Effective gene therapy for an inherited CNS disease in a large animal model.Mannosidosis in Galloway calves.Functional analysis of an alpha-1,2-mannosidase from Magnaporthe oryzae.Swainsonine affects the processing of glycoproteins in vivo.Characterization of alpha-mannosidase in feline mannosidosis.Spontaneous lysosomal storage disease caused by Sida carpinifolia (Malvaceae) poisoning in cattle.Specific inhibition of human beta-D-glucuronidase and alpha-L-iduronidase by a trihydroxy pipecolic acid of plant origin.Alpha-Mannosidosis: Therapeutic Strategies.
P2860
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P2860
description
1980 nî lūn-bûn
@nan
1980年の論文
@ja
1980年論文
@yue
1980年論文
@zh-hant
1980年論文
@zh-hk
1980年論文
@zh-mo
1980年論文
@zh-tw
1980年论文
@wuu
1980年论文
@zh
1980年论文
@zh-cn
name
Biochemical studies on a case of feline mannosidosis.
@en
Biochemical studies on a case of feline mannosidosis.
@nl
type
label
Biochemical studies on a case of feline mannosidosis.
@en
Biochemical studies on a case of feline mannosidosis.
@nl
prefLabel
Biochemical studies on a case of feline mannosidosis.
@en
Biochemical studies on a case of feline mannosidosis.
@nl
P2093
P2860
P356
P1433
P1476
Biochemical studies on a case of feline mannosidosis.
@en
P2093
Blakemore WF
Burditt LJ
Winchester BG
P2860
P304
P356
10.1042/BJ1890467
P407
P577
1980-09-01T00:00:00Z