BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 17428346)

  • 1. Two novel missense mutations in the myostatin gene identified in Japanese patients with Duchenne muscular dystrophy.
    Nishiyama A; Takeshima Y; Saiki K; Narukage A; Oyazato Y; Yagi M; Matsuo M
    BMC Med Genet; 2007 Apr; 8():19. PubMed ID: 17428346
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Altered expression of myostatin gene in the progressive muscular dystrophy patients].
    Zhang Y; Chen Y; Chen JW; Zhu DH
    Yi Chuan Xue Bao; 2005 Aug; 32(8):779-83. PubMed ID: 16231730
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Genotype-phenotype discordance in a Duchenne muscular dystrophy patient due to a novel mutation: insights into the shock absorber function of dystrophin].
    López-Hernández LB; van Heusden D; Soriano-Ursúa MA; Figuera-Villanueva L; Vázquez-Cárdenas NA; Canto P; Gómez-Díaz B; Coral-Vázquez RM
    Rev Neurol; 2011 Jun; 52(12):720-4. PubMed ID: 21594857
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.
    Hofstra RM; Mulder IM; Vossen R; de Koning-Gans PA; Kraak M; Ginjaar IB; van der Hout AH; Bakker E; Buys CH; van Ommen GJ; van Essen AJ; den Dunnen JT
    Hum Mutat; 2004 Jan; 23(1):57-66. PubMed ID: 14695533
    [TBL] [Abstract][Full Text] [Related]  

  • 5. DMD pseudoexon mutations: splicing efficiency, phenotype, and potential therapy.
    Gurvich OL; Tuohy TM; Howard MT; Finkel RS; Medne L; Anderson CB; Weiss RB; Wilton SD; Flanigan KM
    Ann Neurol; 2008 Jan; 63(1):81-9. PubMed ID: 18059005
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Wide ranges of serum myostatin concentrations in Duchenne muscular dystrophy patients.
    Awano H; Takeshima Y; Okizuka Y; Saiki K; Yagi M; Matsuo M
    Clin Chim Acta; 2008 May; 391(1-2):115-7. PubMed ID: 18284920
    [No Abstract]   [Full Text] [Related]  

  • 7. DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy.
    Hamed S; Sutherland-Smith A; Gorospe J; Kendrick-Jones J; Hoffman E
    Clin Genet; 2005 Jul; 68(1):69-79. PubMed ID: 15952989
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic polymorphism in muscle biopsies of Duchenne and Becker muscular dystrophy patients.
    Anand A; Prabhakar S; Kaul D
    Neurol India; 1999 Sep; 47(3):218-23. PubMed ID: 10514583
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis.
    Murugan S; Chandramohan A; Lakshmi BR
    Indian J Med Res; 2010 Sep; 132():303-11. PubMed ID: 20847377
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Point mutation and polymorphism in Duchenne/Becker muscular dystrophy (D/BMD) patients.
    Chaturvedi LS; Mukherjee M; Srivastava S; Mittal RD; Mittal B
    Exp Mol Med; 2001 Dec; 33(4):251-6. PubMed ID: 11795488
    [TBL] [Abstract][Full Text] [Related]  

  • 11. MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients.
    Todorova A; Todorov T; Georgieva B; Lukova M; Guergueltcheva V; Kremensky I; Mitev V
    Neuromuscul Disord; 2008 Aug; 18(8):667-70. PubMed ID: 18653336
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional improvement of dystrophic muscle by myostatin blockade.
    Bogdanovich S; Krag TO; Barton ER; Morris LD; Whittemore LA; Ahima RS; Khurana TS
    Nature; 2002 Nov; 420(6914):418-21. PubMed ID: 12459784
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.
    Takeshima Y; Yagi M; Okizuka Y; Awano H; Zhang Z; Yamauchi Y; Nishio H; Matsuo M
    J Hum Genet; 2010 Jun; 55(6):379-88. PubMed ID: 20485447
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.
    Al-Jumah M; Majumdar R; Al-Rajeh S; Chaves-Carballo E; Salih MM; Awada A; Al-Shahwan S; Al-Uthaim S
    Saudi Med J; 2002 Dec; 23(12):1478-82. PubMed ID: 12518196
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A missense mutant myostatin causes hyperplasia without hypertrophy in the mouse muscle.
    Nishi M; Yasue A; Nishimatu S; Nohno T; Yamaoka T; Itakura M; Moriyama K; Ohuchi H; Noji S
    Biochem Biophys Res Commun; 2002 Apr; 293(1):247-51. PubMed ID: 12054591
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Co-occurrence of mutations in both dystrophin- and androgen-receptor genes is a novel cause of female Duchenne muscular dystrophy.
    Katayama Y; Tran VK; Hoan NT; Zhang Z; Goji K; Yagi M; Takeshima Y; Saiki K; Nhan NT; Matsuo M
    Hum Genet; 2006 Jun; 119(5):516-9. PubMed ID: 16528518
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Study of the gene deletions and the immunofluorescence of muscle in patients with DMD/BMD].
    Dong YH; Lu PY; Wei C; Wang HB; Zhao BH
    Zhongguo Ying Yong Sheng Li Xue Za Zhi; 2005 Nov; 21(4):453-6. PubMed ID: 21180173
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of point mutations in Turkish DMD/BMD families using multiplex-single stranded conformation analysis (SSCA).
    Eraslan S; Kayserili H; Apak MY; Kirdar B
    Eur J Hum Genet; 1999; 7(7):765-70. PubMed ID: 10573008
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Screening of dystrophin gene deletions in Malaysian patients with Duchenne muscular dystrophy.
    Marini M; Salmi AA; Watihayati MS; SMardziah MD; Zahri MK; Hoh BP; Ankathil R; Lai PS; Zilfalil BA
    Med J Malaysia; 2008 Mar; 63(1):31-4. PubMed ID: 18935728
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Early onset of inflammation and later involvement of TGFbeta in Duchenne muscular dystrophy.
    Chen YW; Nagaraju K; Bakay M; McIntyre O; Rawat R; Shi R; Hoffman EP
    Neurology; 2005 Sep; 65(6):826-34. PubMed ID: 16093456
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.