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Author Report for: Oshima A

No contact information in database for Oshima A

    Title: Complete sequencing and characterization of 21,243 full-length human cDNAs
    Ota T, Suzuki Y, Nishikawa T, Otsuki T, Sugiyama T, Irie R, Wakamatsu A, Hayashi K, Sato H and Sugano S <144 more author(s)>
    Ref: Nat Genet, 36:40, 2004 : PubMed


    Title: Protective protein gene mutations in galactosialidosis
    Shimmoto M, Fukuhara Y, Itoh K, Oshima A, Sakuraba H, Suzuki Y
    Ref: J Clinical Investigation, 91:2393, 1993 : PubMed


    Title: A new point mutation of protective protein gene in two Japanese siblings with juvenile galactosialidosis.
    Fukuhara Y, Takano T, Shimmoto M, Oshima A, Takeda E, Kuroda Y, Sakuraba H, Suzuki Y
    Ref: Brain Dysfunction, 5:319, 1992 : PubMed


    Title: Galactosialidosis: clinical and molecular analysis of 19 Japanese patients.
    Takano T, Shimmoto M, Fukuhara Y, Itoh K, Kase R, Takiyama N, Kobayashi T, Oshima A, Sakuraba H, Suzuki Y
    Ref: Brain Dysfunction, 4:271, 1991 : PubMed


    Title: Galactosialidosis: simultaneous deficiency of esterase, carboxy-terminal deamidase and acid carboxypeptidase activities
    Kase R, Itoh K, Takiyama N, Oshima A, Sakuraba H, Suzuki Y
    Ref: Biochemical & Biophysical Research Communications, 172:1175, 1990 : PubMed


    Title: Japanese-type adult galactosialidosis: a unique and common splice junction mutation causing exon skipping in the protective protein/carboxypeptidase gene
    Shimmoto M, Takano T, Fukuhara Y, Oshima A, Sakuraba H, Suzuki Y
    Ref: Proc Jpn Acad, 66B:217, 1990 : PubMed


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