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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1995-6-29
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pubmed:databankReference | |
pubmed:abstractText |
Amphiphysin is a protein peripherally associated with synaptic vesicles. It is expressed in many neurons, certain endocrine cell types, and spermatocytes. Autoantibodies against amphiphysin occur in patients afflicted with a rare neurologic autoimmune disease, paraneoplastic Stiff-Man syndrome. To provide a basis for the understanding of anti-amphiphysin autoimmunity, we have cloned cDNAs and determined the primary structure of human amphiphysin. Comparison with chicken amphiphysin defines domains of low and high amino acid sequence conservation. As a candidate for heritable disorders of the nervous system, endocrine tissues or male fertility, the human amphiphysin gene was mapped to chromosome 7, region p13-p14.
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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 |
Feb
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pubmed:issn |
0964-6906
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
4
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
265-8
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:7757077-Animals,
pubmed-meshheading:7757077-Autoantigens,
pubmed-meshheading:7757077-Base Sequence,
pubmed-meshheading:7757077-Chickens,
pubmed-meshheading:7757077-Chromosome Mapping,
pubmed-meshheading:7757077-Chromosomes, Human, Pair 7,
pubmed-meshheading:7757077-Cloning, Molecular,
pubmed-meshheading:7757077-Cricetinae,
pubmed-meshheading:7757077-DNA, Complementary,
pubmed-meshheading:7757077-Genes, Dominant,
pubmed-meshheading:7757077-Humans,
pubmed-meshheading:7757077-Molecular Sequence Data,
pubmed-meshheading:7757077-Nerve Tissue Proteins,
pubmed-meshheading:7757077-Sequence Homology, Amino Acid,
pubmed-meshheading:7757077-Stiff-Person Syndrome
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pubmed:year |
1995
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pubmed:articleTitle |
Primary structure of human amphiphysin, the dominant autoantigen of paraneoplastic stiff-man syndrome, and mapping of its gene (AMPH) to chromosome 7p13-p14.
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pubmed:affiliation |
Institut für Physiologische Chemie, Medizinische Fakultät, Ruhr-Universität Bochum, Germany.
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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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