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 *

226 related articles for article (PubMed ID: 8900232)

  • 21. [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]  

  • 22. A first missense mutation in the delta sarcoglycan gene associated with a severe phenotype and frequency of limb-girdle muscular dystrophy type 2F (LGMD2F) in Brazilian sarcoglycanopathies.
    Moreira ES; Vainzof M; Marie SK; Nigro V; Zatz M; Passos-Bueno MR
    J Med Genet; 1998 Nov; 35(11):951-3. PubMed ID: 9832045
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
    Nigro V; de Sá Moreira E; Piluso G; Vainzof M; Belsito A; Politano L; Puca AA; Passos-Bueno MR; Zatz M
    Nat Genet; 1996 Oct; 14(2):195-8. PubMed ID: 8841194
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene.
    McNally EM; Ly CT; Kunkel LM
    FEBS Lett; 1998 Jan; 422(1):27-32. PubMed ID: 9475163
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile.
    Bönnemann CG; Wong J; Jones KJ; Lidov HG; Feener CA; Shapiro F; Darras BT; Kunkel LM; North KN
    Neuromuscul Disord; 2002 Mar; 12(3):273-80. PubMed ID: 11801399
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy.
    Sewry CA; Taylor J; Anderson LV; Ozawa E; Pogue R; Piccolo F; Bushby K; Dubowitz V; Muntoni F
    Neuromuscul Disord; 1996 Dec; 6(6):467-74. PubMed ID: 9027857
    [TBL] [Abstract][Full Text] [Related]  

  • 27. alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations.
    Duggan DJ; Fanin M; Pegoraro E; Angelini C; Hoffman EP
    J Neurol Sci; 1996 Sep; 140(1-2):30-9. PubMed ID: 8866424
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Sarcoglycans in muscular dystrophy.
    Hack AA; Groh ME; McNally EM
    Microsc Res Tech; 2000 Feb 1-15; 48(3-4):167-80. PubMed ID: 10679964
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy.
    Jung D; Duclos F; Apostol B; Straub V; Lee JC; Allamand V; Venzke DP; Sunada Y; Moomaw CR; Leveille CJ; Slaughter CA; Crawford TO; McPherson JD; Campbell KP
    J Biol Chem; 1996 Dec; 271(50):32321-9. PubMed ID: 8943294
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families.
    Dinçer P; Akçören Z; Demir E; Richard I; Sancak O; Kale G; Ozme S; Karaduman A; Tan E; Urtizberea JA; Beckmann JS; Topaloğlu H
    J Med Genet; 2000 May; 37(5):361-7. PubMed ID: 10807695
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy.
    Ginjaar HB; van der Kooi AJ; Ceelie H; Kneppers AL; van Meegen M; Barth PG; Busch HF; Wokke JH; Anderson LV; Bönnemann CG; Jeanpierre M; Bolhuis PA; Moorman AF; de Visser M; Bakker E; Ommen GJ
    J Neurol; 2000 Jul; 247(7):524-9. PubMed ID: 10993494
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
    Vainzof M; Passos-Bueno MR; Canovas M; Moreira ES; Pavanello RC; Marie SK; Anderson LV; Bonnemann CG; McNally EM; Nigro V; Kunkel LM; Zatz M
    Hum Mol Genet; 1996 Dec; 5(12):1963-9. PubMed ID: 8968750
    [TBL] [Abstract][Full Text] [Related]  

  • 33. New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency.
    Higuchi I; Iwaki H; Kawai H; Endo T; Kunishige M; Fukunaga H; Nakagawa M; Arimura K; Osame M
    J Neurol Sci; 1997 Dec; 153(1):100-5. PubMed ID: 9455986
    [TBL] [Abstract][Full Text] [Related]  

  • 34. On symptomatic heterozygous alpha-sarcoglycan gene mutation carriers.
    Fischer D; Aurino S; Nigro V; Schröder R
    Ann Neurol; 2003 Nov; 54(5):674-8. PubMed ID: 14595658
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern Italy.
    Fanin M; Hoffman EP; Angelini C; Pegoraro E
    Hum Mutat; 2000; 16(1):13-7. PubMed ID: 10874299
    [TBL] [Abstract][Full Text] [Related]  

  • 37. epsilon-Sarcoglycan, a broadly expressed homologue of the gene mutated in limb-girdle muscular dystrophy 2D.
    Ettinger AJ; Feng G; Sanes JR
    J Biol Chem; 1997 Dec; 272(51):32534-8. PubMed ID: 9405466
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Loss of sarcolemma nNOS in sarcoglycan-deficient muscle.
    Crosbie RH; Barresi R; Campbell KP
    FASEB J; 2002 Nov; 16(13):1786-91. PubMed ID: 12409321
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Adhalin(alpha-sarcoglycan) gene mutations in patients with malignant limb-girdle muscular dystrophy (MLGMD) (Miyoshi)].
    Endo T; Kawai H
    Nihon Rinsho; 1997 Dec; 55(12):3159-64. PubMed ID: 9436428
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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; 381(1-2):15-20. PubMed ID: 8641426
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.