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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2-3
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pubmed:dateCreated |
1995-8-14
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pubmed:databankReference | |
pubmed:abstractText |
Mucopolysaccharidosis IIID results from the deficiency of N-acetylglucosamine 6-sulfatase activity. A Nubian goat with this lysosomal storage disease has been identified. As a first step in developing this animal model for testing treatment methods, we cloned and sequenced the caprine N-acetylglucosamine 6-sulfatase cDNA coding region. Overall there is 88% nucleotide homology between the goat and human sequence and 94% homology of the deduced amino acid sequence. The human and two ruminant species differ by the presence of an imperfect trinucleotide (CCG) repeat in the ruminant signal sequence.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0006-3002
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
9
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pubmed:volume |
1271
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
369-73
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:7605804-Amino Acid Sequence,
pubmed-meshheading:7605804-Animals,
pubmed-meshheading:7605804-Base Sequence,
pubmed-meshheading:7605804-Cloning, Molecular,
pubmed-meshheading:7605804-DNA, Complementary,
pubmed-meshheading:7605804-Goats,
pubmed-meshheading:7605804-Molecular Sequence Data,
pubmed-meshheading:7605804-Mucopolysaccharidosis III,
pubmed-meshheading:7605804-Sequence Homology, Amino Acid,
pubmed-meshheading:7605804-Sequence Homology, Nucleic Acid,
pubmed-meshheading:7605804-Sulfatases
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pubmed:year |
1995
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pubmed:articleTitle |
Cloning and sequence analysis of caprine N-acetylglucosamine 6-sulfatase cDNA.
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pubmed:affiliation |
Department of Pathology, Michigan State University, East Lansing 48824-1314, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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