These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

106 related articles for article (PubMed ID: 7758576)

  • 1. Adhalin mRNA and cDNA sequence are normal in the cardiomyopathic hamster.
    Roberds SL; Campbell KP
    FEBS Lett; 1995 May; 364(3):245-9. PubMed ID: 7758576
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 235(1):227-35. PubMed ID: 9196068
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 96(3):1202-7. PubMed ID: 7657792
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy.
    Roberds SL; Leturcq F; Allamand V; Piccolo F; Jeanpierre M; Anderson RD; Lim LE; Lee JC; Tomé FM; Romero NB
    Cell; 1994 Aug; 78(4):625-33. PubMed ID: 8069911
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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; 36(3):415-22. PubMed ID: 8741343
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 38(3):367-72. PubMed ID: 7668821
    [TBL] [Abstract][Full Text] [Related]  

  • 7. mRNA expression and cDNA sequences of beta- and gamma-sarcoglycans are normal in cardiomyopathic hamster heart.
    Hanada H; Yoshida T; Pan Y; Iwata Y; Nishimura M; Shigekawa M
    Biol Pharm Bull; 1997 Feb; 20(2):134-7. PubMed ID: 9057973
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical heterogeneity of adhalin deficiency.
    Morandi L; Barresi R; Di Blasi C; Jung D; Sunada Y; Confalonieri V; Dworzak F; Mantegazza R; Antozzi C; Jarre L; Pini A; Gobbi G; Bianchi C; Cornelio F; Campbell KP; Mora M
    Ann Neurol; 1996 Feb; 39(2):196-202. PubMed ID: 8967751
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 11(3):257-65. PubMed ID: 7581448
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 91(21):9690-4. PubMed ID: 7937874
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular pathogenesis of muscle degeneration in the delta-sarcoglycan-deficient hamster.
    Straub V; Duclos F; Venzke DP; Lee JC; Cutshall S; Leveille CJ; Campbell KP
    Am J Pathol; 1998 Nov; 153(5):1623-30. PubMed ID: 9811355
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 268(32):23739-42. PubMed ID: 8226900
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex.
    Sakamoto A; Ono K; Abe M; Jasmin G; Eki T; Murakami Y; Masaki T; Toyo-oka T; Hanaoka F
    Proc Natl Acad Sci U S A; 1997 Dec; 94(25):13873-8. PubMed ID: 9391120
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 4(7):1163-7. PubMed ID: 8528203
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Increased expression of the gene for alpha-interferon-inducible protein in cardiomyopathic hamster heart.
    Denovan-Wright EM; Ferrier GR; Robertson HA; Howlett SE
    Biochem Biophys Res Commun; 2000 Jan; 267(1):103-8. PubMed ID: 10623582
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy.
    Durbeej M; Sawatzki SM; Barresi R; Schmainda KM; Allamand V; Michele DE; Campbell KP
    Proc Natl Acad Sci U S A; 2003 Jul; 100(15):8910-5. PubMed ID: 12851463
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy.
    Eymard B; Romero NB; Leturcq F; Piccolo F; Carrié A; Jeanpierre M; Collin H; Deburgrave N; Azibi K; Chaouch M; Merlini L; Thémar-Noël C; Penisson I; Mayer M; Tanguy O; Campbell KP; Kaplan JC; Tomé FM; Fardeau M
    Neurology; 1997 May; 48(5):1227-34. PubMed ID: 9153448
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity.
    Piccolo F; Roberds SL; Jeanpierre M; Leturcq F; Azibi K; Beldjord C; Carrié A; Récan D; Chaouch M; Reghis A
    Nat Genet; 1995 Jun; 10(2):243-5. PubMed ID: 7663524
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Electron microscopic observations of triple immunogold labelling for dystrophin, beta-dystroglycan and adhalin in human skeletal myofibers.
    Inoue M; Wakayama Y; Murahashi M; Shibuya S; Jimi T; Kojima H; Oniki H
    Acta Neuropathol; 1996 Dec; 92(6):569-75. PubMed ID: 8960314
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The frequency of patients with adhalin deficiency in a muscular dystrophy patient population].
    Hayashi YK; Arahata K
    Nihon Rinsho; 1997 Dec; 55(12):3165-8. PubMed ID: 9436429
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.