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 *

145 related articles for article (PubMed ID: 10874299)

  • 21. Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation.
    Kefi M; Amouri R; Driss A; Ben Hamida C; Ben Hamida M; Kunkel LM; Hentati F
    Neuromuscul Disord; 2003 Dec; 13(10):779-87. PubMed ID: 14678800
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Expression of gamma -sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex.
    Barresi R; Moore SA; Stolle CA; Mendell JR; Campbell KP
    J Biol Chem; 2000 Dec; 275(49):38554-60. PubMed ID: 10993904
    [TBL] [Abstract][Full Text] [Related]  

  • 23. LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3.
    Bönnemann CG; Wong J; Ben Hamida C; Hamida MB; Hentati F; Kunkel LM
    Neuromuscul Disord; 1998 May; 8(3-4):193-7. PubMed ID: 9631401
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Sarcoglycanopathies are responsible for 68% of severe autosomal recessive limb-girdle muscular dystrophy in the Brazilian population.
    Vainzof M; Passos-Bueno MR; Pavanello RC; Marie SK; Oliveira AS; Zatz M
    J Neurol Sci; 1999 Mar; 164(1):44-9. PubMed ID: 10385046
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. [Gene analysis in patients with muscular dystrophy: alpha-sarcoglycan (adhalin) gene mutations in patients with malignant limb-girdle muscular dystrophy].
    Akaike M; Kawai H
    Rinsho Byori; 1997 Feb; 45(2):136-40. PubMed ID: 9120997
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. 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]  

  • 29. [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]  

  • 30. Specific assembly pathway of sarcoglycans is dependent on beta- and delta-sarcoglycan.
    Shi W; Chen Z; Schottenfeld J; Stahl RC; Kunkel LM; Chan YM
    Muscle Nerve; 2004 Mar; 29(3):409-19. PubMed ID: 14981741
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy.
    Pegoraro E; Fanin M; Angelini C; Hoffman EP
    Neuromuscul Disord; 1999 Jul; 9(5):323-5. PubMed ID: 10407854
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Extraocular muscle is spared despite the absence of an intact sarcoglycan complex in gamma- or delta-sarcoglycan-deficient mice.
    Porter JD; Merriam AP; Hack AA; Andrade FH; McNally EM
    Neuromuscul Disord; 2001 Mar; 11(2):197-207. PubMed ID: 11257478
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate.
    Duclos F; Broux O; Bourg N; Straub V; Feldman GL; Sunada Y; Lim LE; Piccolo F; Cutshall S; Gary F; Quetier F; Kaplan JC; Jackson CE; Beckmann JS; Campbell KP
    Neuromuscul Disord; 1998 Feb; 8(1):30-8. PubMed ID: 9565988
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Overexpression of gamma-sarcoglycan induces severe muscular dystrophy. Implications for the regulation of Sarcoglycan assembly.
    Zhu X; Hadhazy M; Groh ME; Wheeler MT; Wollmann R; McNally EM
    J Biol Chem; 2001 Jun; 276(24):21785-90. PubMed ID: 11287429
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Deficiency of the 50 kDa dystrophin-associated-glycoprotein (adhalin) in an Indian autosomal recessive limb girdle muscular dystrophy patient : immunochemical analysis and clinical aspects.
    Handa V; Mital A; Gupta M; Goyle S
    Neurol India; 2001 Mar; 49(1):19-24. PubMed ID: 11303236
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.
    Araishi K; Sasaoka T; Imamura M; Noguchi S; Hama H; Wakabayashi E; Yoshida M; Hori T; Ozawa E
    Hum Mol Genet; 1999 Sep; 8(9):1589-98. PubMed ID: 10441321
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D).
    Carrié A; Piccolo F; Leturcq F; de Toma C; Azibi K; Beldjord C; Vallat JM; Merlini L; Voit T; Sewry C; Urtizberea JA; Romero N; Tomé FM; Fardeau M; Sunada Y; Campbell KP; Kaplan JC; Jeanpierre M
    J Med Genet; 1997 Jun; 34(6):470-5. PubMed ID: 9192266
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.