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 *

144 related articles for article (PubMed ID: 9611069)

  • 1. Skewed X inactivation in manifesting carriers of Duchenne muscular dystrophy.
    Yoshioka M; Yorifuji T; Mituyoshi I
    Clin Genet; 1998 Feb; 53(2):102-7. PubMed ID: 9611069
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.
    Sumita DR; Vainzof M; Campiotto S; Cerqueira AM; Cánovas M; Otto PA; Passos-Bueno MR; Zatz M
    Am J Med Genet; 1998 Dec; 80(4):356-61. PubMed ID: 9856563
    [TBL] [Abstract][Full Text] [Related]  

  • 3. X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes.
    Azofeifa J; Voit T; Hübner C; Cremer M
    Hum Genet; 1995 Aug; 96(2):167-76. PubMed ID: 7635465
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Skewed X-chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy.
    Viggiano E; Picillo E; Ergoli M; Cirillo A; Del Gaudio S; Politano L
    J Gene Med; 2017 Apr; 19(4):. PubMed ID: 28316128
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy.
    Lupski JR; Garcia CA; Zoghbi HY; Hoffman EP; Fenwick RG
    Am J Med Genet; 1991 Sep; 40(3):354-64. PubMed ID: 1683155
    [TBL] [Abstract][Full Text] [Related]  

  • 6. X-inactivation patterns in carriers of X-linked myotubular myopathy.
    Kristiansen M; Knudsen GP; Tanner SM; McEntagart M; Jungbluth H; Muntoni F; Sewry C; Gallati S; Ørstavik KH; Wallgren-Pettersson C
    Neuromuscul Disord; 2003 Aug; 13(6):468-71. PubMed ID: 12899873
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Comparison of X-chromosome inactivation in Duchenne muscle/myocardium-manifesting carriers, non-manifesting carriers and related daughters.
    Viggiano E; Picillo E; Cirillo A; Politano L
    Clin Genet; 2013 Sep; 84(3):265-70. PubMed ID: 23110537
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical features and skewed X-chromosome inactivation in female carriers of X-linked recessive spinal and bulbar muscular atrophy.
    Ishihara H; Kanda F; Nishio H; Sumino K; Chihara K
    J Neurol; 2001 Oct; 248(10):856-60. PubMed ID: 11697521
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei.
    Pegoraro E; Schimke RN; Garcia C; Stern H; Cadaldini M; Angelini C; Barbosa E; Carroll J; Marks WA; Neville HE; Marks H; Appleton S; Toriello H; Wessel HB; Donnelly J; Bernes SM; Taber JW; Weiss L; Hoffman EP
    Neurology; 1995 Apr; 45(4):677-90. PubMed ID: 7723955
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers.
    Matthews PM; Benjamin D; Van Bakel I; Squier MV; Nicholson LV; Sewry C; Barnes PR; Hopkin J; Brown R; Hilton-Jones D
    Neuromuscul Disord; 1995 May; 5(3):209-20. PubMed ID: 7633186
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Manifesting carriers of Duchenne muscular dystrophy over two generations].
    Itagaki Y; Saida K; Nishitani H; Matsuo M; Nishio H
    Rinsho Shinkeigaku; 1993 Apr; 33(4):377-81. PubMed ID: 8103723
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy.
    Richards CS; Watkins SC; Hoffman EP; Schneider NR; Milsark IW; Katz KS; Cook JD; Kunkel LM; Cortada JM
    Am J Hum Genet; 1990 Apr; 46(4):672-81. PubMed ID: 2180286
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Symptomatic female carriers of Duchenne muscular dystrophy (DMD): genetic and clinical characterization.
    Giliberto F; Radic CP; Luce L; Ferreiro V; de Brasi C; Szijan I
    J Neurol Sci; 2014 Jan; 336(1-2):36-41. PubMed ID: 24135430
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.
    Lose F; Duffy DL; Kay GF; Kedda MA; Spurdle AB; ;
    J Natl Cancer Inst; 2008 Nov; 100(21):1519-29. PubMed ID: 18957670
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of new paternal dystrophin gene mutations in isolated cases of dystrophinopathy in females.
    Pegoraro E; Schimke RN; Arahata K; Hayashi Y; Stern H; Marks H; Glasberg MR; Carroll JE; Taber JW; Wessel HB
    Am J Hum Genet; 1994 Jun; 54(6):989-1003. PubMed ID: 8198142
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype.
    Brioschi S; Gualandi F; Scotton C; Armaroli A; Bovolenta M; Falzarano MS; Sabatelli P; Selvatici R; D'Amico A; Pane M; Ricci G; Siciliano G; Tedeschi S; Pini A; Vercelli L; De Grandis D; Mercuri E; Bertini E; Merlini L; Mongini T; Ferlini A
    BMC Med Genet; 2012 Aug; 13():73. PubMed ID: 22894145
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Brother/sister siblings affected with Hunter disease: evidence for skewed X chromosome inactivation.
    Sukegawa K; Matsuzaki T; Fukuda S; Masuno M; Fukao T; Kokuryu M; Iwata S; Tomatsu S; Orii T; Kondo N
    Clin Genet; 1998 Feb; 53(2):96-101. PubMed ID: 9611068
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.
    Allen RC; Zoghbi HY; Moseley AB; Rosenblatt HM; Belmont JW
    Am J Hum Genet; 1992 Dec; 51(6):1229-39. PubMed ID: 1281384
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A female carrier of a novel DMD mutation with slightly skewed X-chromosome inactivation shows a suspected case of Becker muscular dystrophy in a Chinese family.
    Chen J; Zheng H; Wang Z; Wang J; He F; Zhang C; Xiong F
    Mol Genet Genomics; 2021 May; 296(3):541-549. PubMed ID: 33566169
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Skewed X-inactivation in carriers of X-linked dyskeratosis congenita.
    Vulliamy TJ; Knight SW; Dokal I; Mason PJ
    Blood; 1997 Sep; 90(6):2213-6. PubMed ID: 9310472
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.