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Journal Abstract Search

174 related items for PubMed ID: 7937874

  • 1. Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.
    McNally EM, Yoshida M, Mizuno Y, Ozawa E, Kunkel LM.
    Proc Natl Acad Sci U S A; 1994 Oct 11; 91(21):9690-4. PubMed ID: 7937874
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  • 3. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy.
    Bueno MR, Moreira ES, Vainzof M, Chamberlain J, Marie SK, Pereira L, Akiyama J, Roberds SL, Campbell KP, Zatz M.
    Hum Mol Genet; 1995 Jul 11; 4(7):1163-7. PubMed ID: 8528203
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  • 4. Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.
    Kawai H, Akaike M, Endo T, Adachi K, Inui T, Mitsui T, Kashiwagi S, Fujiwara T, Okuno S, Shin S.
    J Clin Invest; 1995 Sep 11; 96(3):1202-7. PubMed ID: 7657792
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  • 6. [Adhalin gene mutations in malignant limb-girdle muscular dystrophy and clinical features in adhalin-deficient muscular dystrophy].
    Endo T, Akaike M, Kawai H, Matsumura K, Saito S.
    Rinsho Shinkeigaku; 1996 Mar 11; 36(3):415-22. PubMed ID: 8741343
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  • 8. Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin.
    Ljunggren A, Duggan D, McNally E, Boylan KB, Gama CH, Kunkel LM, Hoffman EP.
    Ann Neurol; 1995 Sep 11; 38(3):367-72. PubMed ID: 7668821
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  • 9. Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy.
    Noguchi S, McNally EM, Ben Othmane K, Hagiwara Y, Mizuno Y, Yoshida M, Yamamoto H, Bönnemann CG, Gussoni E, Denton PH, Kyriakides T, Middleton L, Hentati F, Ben Hamida M, Nonaka I, Vance JM, Kunkel LM, Ozawa E.
    Science; 1995 Nov 03; 270(5237):819-22. PubMed ID: 7481775
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  • 10. Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12.
    Lim LE, Duclos F, Broux O, Bourg N, Sunada Y, Allamand V, Meyer J, Richard I, Moomaw C, Slaughter C.
    Nat Genet; 1995 Nov 03; 11(3):257-65. PubMed ID: 7581448
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  • 11. Laminin abnormality in severe childhood autosomal recessive muscular dystrophy.
    Yamada H, Tomé FM, Higuchi I, Kawai H, Azibi K, Chaouch M, Roberds SL, Tanaka T, Fujita S, Mitsui T.
    Lab Invest; 1995 Jun 03; 72(6):715-22. PubMed ID: 7783429
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  • 13. Mouse adhalin: primary structure and expression during late stages of muscle differentiation in vitro.
    Liu L, Vachon PH, Kuang W, Xu H, Wewer UM, Kylsten P, Engvall E.
    Biochem Biophys Res Commun; 1997 Jun 09; 235(1):227-35. PubMed ID: 9196068
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  • 16. [Adhalin(alpha-sarcoglycan) gene mutations in patients with malignant limb-girdle muscular dystrophy (MLGMD) (Miyoshi)].
    Endo T, Kawai H.
    Nihon Rinsho; 1997 Dec 09; 55(12):3159-64. PubMed ID: 9436428
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  • 18. Primary structure and muscle-specific expression of the 50-kDa dystrophin-associated glycoprotein (adhalin).
    Roberds SL, Anderson RD, Ibraghimov-Beskrovnaya O, Campbell KP.
    J Biol Chem; 1993 Nov 15; 268(32):23739-42. PubMed ID: 8226900
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  • 19. Absence of gamma-sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12.
    Jung D, Leturcq F, Sunada Y, Duclos F, Tomé FM, Moomaw C, Merlini L, Azibi K, Chaouch M, Slaughter C, Fardeau M, Kaplan JC, Campbell KP.
    FEBS Lett; 1996 Feb 26; 381(1-2):15-20. PubMed ID: 8641426
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