BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 10682317)

  • 1. Fukuyama-type congenital muscular dystrophy: the first human disease to be caused by an ancient retrotransposal integration.
    Toda T; Kobayashi K
    J Mol Med (Berl); 1999 Dec; 77(12):816-23. PubMed ID: 10682317
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Fukuyama congenital muscular dystrophy story.
    Toda T; Kobayashi K; Kondo-Iida E; Sasaki J; Nakamura Y
    Neuromuscul Disord; 2000 Mar; 10(3):153-9. PubMed ID: 10734260
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.
    Kobayashi K; Nakahori Y; Miyake M; Matsumura K; Kondo-Iida E; Nomura Y; Segawa M; Yoshioka M; Saito K; Osawa M; Hamano K; Sakakihara Y; Nonaka I; Nakagome Y; Kanazawa I; Nakamura Y; Tokunaga K; Toda T
    Nature; 1998 Jul; 394(6691):388-92. PubMed ID: 9690476
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD).
    Kondo-Iida E; Kobayashi K; Watanabe M; Sasaki J; Kumagai T; Koide H; Saito K; Osawa M; Nakamura Y; Toda T
    Hum Mol Genet; 1999 Nov; 8(12):2303-9. PubMed ID: 10545611
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Fukuyama-type congenital muscular dystrophy].
    Toda T
    Rinsho Shinkeigaku; 2000 Dec; 40(12):1297-9. PubMed ID: 11464484
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Hint and luck for identification of a gene for Fukuyama muscular dystrophy, fukutin].
    Toda T
    Rinsho Shinkeigaku; 2007 Nov; 47(11):743-8. PubMed ID: 18210789
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A rapid diagnostic method for a retrotransposal insertional mutation into the FCMD gene in Japanese patients with Fukuyama congenital muscular dystrophy.
    Kato R; Kawamura J; Sugawara H; Niikawa N; Matsumoto N
    Am J Med Genet A; 2004 May; 127A(1):54-57. PubMed ID: 15103718
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Age and origin of the FCMD 3'-untranslated-region retrotransposal insertion mutation causing Fukuyama-type congenital muscular dystrophy in the Japanese population.
    Colombo R; Bignamini AA; Carobene A; Sasaki J; Tachikawa M; Kobayashi K; Toda T
    Hum Genet; 2000 Dec; 107(6):559-67. PubMed ID: 11153909
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Fukutin gene retrotransposal insertion in a non-Japanese Fukuyama congenital muscular dystrophy (FCMD) patient.
    Xiong H; Wang S; Kobayashi K; Jiang Y; Wang J; Chang X; Yuan Y; Liu J; Toda T; Fukuyama Y; Wu X
    Am J Med Genet A; 2009 Nov; 149A(11):2403-8. PubMed ID: 19842201
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Founder SVA retrotransposal insertion in Fukuyama-type congenital muscular dystrophy and its origin in Japanese and Northeast Asian populations.
    Watanabe M; Kobayashi K; Jin F; Park KS; Yamada T; Tokunaga K; Toda T
    Am J Med Genet A; 2005 Nov; 138(4):344-8. PubMed ID: 16222679
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical and genetic analysis of a Korean patient with Fukuyama congenital muscular dystrophy.
    Lee J; Lee BL; Lee M; Kim JH; Kim JW; Ki CS
    J Neurol Sci; 2009 Jun; 281(1-2):122-4. PubMed ID: 19324374
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)].
    Toda T; Kobayashi K
    Nihon Rinsho; 1997 Dec; 55(12):3169-75. PubMed ID: 9436430
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.
    Toda T; Yoshioka M; Nakahori Y; Kanazawa I; Nakamura Y; Nakagome Y
    Ann Neurol; 1995 Jan; 37(1):99-101. PubMed ID: 7818265
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenotypic spectrum of Fukutinopathy: most severe phenotype of Fukutinopathy.
    Yoshioka M
    Brain Dev; 2009 Jun; 31(6):419-22. PubMed ID: 18834683
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD).
    Kobayashi K; Nakahori Y; Mizuno K; Miyake M; Kumagai T; Honma A; Nonaka I; Nakamura Y; Tokunaga K; Toda T
    Hum Genet; 1998 Sep; 103(3):323-7. PubMed ID: 9799088
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Broader clinical spectrum of Fukuyama-type congenital muscular dystrophy manifested by haplotype analysis.
    Yoshioka M; Toda T; Kuroki S; Hamano K
    J Child Neurol; 1999 Nov; 14(11):711-5. PubMed ID: 10593547
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin.
    Kobayashi K; Sasaki J; Kondo-Iida E; Fukuda Y; Kinoshita M; Sunada Y; Nakamura Y; Toda T
    FEBS Lett; 2001 Feb; 489(2-3):192-6. PubMed ID: 11165248
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.
    Toda T; Miyake M; Kobayashi K; Mizuno K; Saito K; Osawa M; Nakamura Y; Kanazawa I; Nakagome Y; Tokunaga K; Nakahori Y
    Am J Hum Genet; 1996 Dec; 59(6):1313-20. PubMed ID: 8940277
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fukutin protein is expressed in neurons of the normal developing human brain but is reduced in Fukuyama-type congenital muscular dystrophy brain.
    Saito Y; Mizuguchi M; Oka A; Takashima S
    Ann Neurol; 2000 Jun; 47(6):756-64. PubMed ID: 10852541
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic.
    Ranta S; Pihko H; Santavuori P; Tahvanainen E; de la Chapelle A
    Neuromuscul Disord; 1995 May; 5(3):221-5. PubMed ID: 7633187
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.