about
P688
Murine mucopolysaccharidosis type I: targeted disruption of the murine alpha-L-iduronidase geneEvidence of a progressive motor dysfunction in Mucopolysaccharidosis type I mice.Progression of multiple behavioral deficits with various ages of onset in a murine model of Hurler syndrome.Mucopolysaccharidosis type I, unique structure of accumulated heparan sulfate and increased N-sulfotransferase activity in mice lacking α-l-iduronidase.Glycosaminoglycan-mediated loss of cathepsin K collagenolytic activity in MPS I contributes to osteoclast and growth plate abnormalities.Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutation.Effect of neonatal administration of a retroviral vector expressing alpha-L-iduronidase upon lysosomal storage in brain and other organs in mucopolysaccharidosis I mice.Extracellular matrix disruption is an early event in the pathogenesis of skeletal disease in mucopolysaccharidosis I.
P921
Q28504642-D27F8B79-AEB1-438C-B353-C9509D3D015AQ30452225-FD1500C5-7B5A-44B1-AFF9-5C149C6A0E11Q30491775-A17A52B0-F5CA-4C69-AEED-351706FB9018Q35423844-173A1E42-D1ED-492E-A5B2-9C6CB6701499Q37413691-7A12FDD6-3CA6-4132-AD2C-C18ED10942B7Q37480537-01C19BE5-2C56-4EE6-B246-5DCD41C850D8Q45170206-B025B1D5-4CC0-4C4E-B03E-EA64F7D2DEDAQ46139975-7005ACFA-06CC-4CF9-93B7-E46C9E950749
P921
description
mouse protein (annotated by UniProtKB/Swiss-Prot P48441)
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proteinë
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proteïne
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بروتين في فأر المنازل
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name
Alpha-L-iduronidase
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type
label
Alpha-L-iduronidase
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prefLabel
Alpha-L-iduronidase
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