Literature DB >> 7757077

Primary structure of human amphiphysin, the dominant autoantigen of paraneoplastic stiff-man syndrome, and mapping of its gene (AMPH) to chromosome 7p13-p14.

R Yamamoto1, X Li, S Winter, U Francke, M W Kilimann.   

Abstract

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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Year:  1995        PMID: 7757077     DOI: 10.1093/hmg/4.2.265

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  5 in total

1.  Stiff-man syndrome.

Authors:  H U Rehman
Journal:  Postgrad Med J       Date:  1998-11       Impact factor: 2.401

Review 2.  Autoimmune stiff person syndrome and related myelopathies: understanding of electrophysiological and immunological processes.

Authors:  Goran Rakocevic; Mary Kay Floeter
Journal:  Muscle Nerve       Date:  2012-05       Impact factor: 3.217

3.  The crystal structure of the BAR domain from human Bin1/amphiphysin II and its implications for molecular recognition.

Authors:  Eva Casal; Luca Federici; Wei Zhang; Juan Fernandez-Recio; Eva-Maria Priego; Ricardo Nuñez Miguel; James B DuHadaway; George C Prendergast; Ben F Luisi; Ernest D Laue
Journal:  Biochemistry       Date:  2006-10-31       Impact factor: 3.162

4.  Amphiphysin I but not dynamin I nor synaptojanin mRNA expression increased after repeated methamphetamine administration in the rat cerebrum and cerebellum.

Authors:  Mitsuko Hamamura; Jiro Okouchi; Hidetoshi Ozawa; Yoshihiko Kimuro; Akiko Iwaki; Yasuyuki Fukumaki
Journal:  J Neural Transm (Vienna)       Date:  2012-12-08       Impact factor: 3.575

5.  Genetic mapping of the human amphiphysin gene (AMPH) at 7p14-p13 excludes its involvement in retinitis pigmentosa 9 or dominant cystoid macular dystrophy.

Authors:  R Yamamoto; X Li; U Francke; M W Kilimann
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

  5 in total

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