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 *

85 related articles for article (PubMed ID: 3565471)

  • 1. Metaphase chromosome folds and X-inactivation.
    Butler MG; Joseph GM; Dev VG
    Am J Med Genet; 1987 Mar; 26(3):565-8. PubMed ID: 3565471
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The human inactivated X chromosome folds in early metaphase, prometaphase, and prophase.
    Van Dyke DL; Worsham M; Weiss L
    Hum Genet; 1987 Sep; 77(1):57-9. PubMed ID: 3623560
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Bends in human mitotic metaphase chromosomes, including a bend marking the X-inactivation center.
    Flejter WL; Van Dyke DL; Weiss L
    Am J Hum Genet; 1984 Jan; 36(1):218-26. PubMed ID: 6582784
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A practical metaphase marker of the inactive X chromosome.
    Van Dyke DL; Flejter WL; Worsham MJ; Roberson JR; Higgins JV; Herr HM; Knuutila S; Wang N; Babu VR; Weiss L
    Am J Hum Genet; 1986 Jul; 39(1):88-95. PubMed ID: 3463206
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Location of the X inactivation center in primates and other mammals.
    Flejter WL; Van Dyke DL; Weiss L
    Hum Genet; 1986 Sep; 74(1):63-6. PubMed ID: 3759086
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
    Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
    Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
    [TBL] [Abstract][Full Text] [Related]  

  • 7. X chromosome inactivation in bone marrow cells of adult mice carrying Searle's X-autosome translocation: occurrence of the early-replicating inactive X chromosome.
    Takagi N; Endo S; Sugawara O
    Cytogenet Cell Genet; 1984; 38(1):62-9. PubMed ID: 6705567
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Inhibition of condensation in the late-replicating X chromosome induced by 5-azadeoxycytidine in human lymphocyte cultures.
    Haaf T; Ott G; Schmid M
    Hum Genet; 1988 May; 79(1):18-23. PubMed ID: 2452785
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular characterization of a deleted X chromosome (Xq13.3-Xq21.31) exhibiting random X inactivation.
    Migeon BR; Stetten G; Tuck-Muller C; Axelman J; Jani M; Dungy D
    Somat Cell Mol Genet; 1995 Mar; 21(2):113-20. PubMed ID: 7570183
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Inactivation centers in the human X chromosome.
    Nakagome Y
    Am J Hum Genet; 1982 Mar; 34(2):182-94. PubMed ID: 6985472
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Position of late and early replicating human X chromosomes at somatic metaphase.
    Dosik D; Babu KA; Verma RS
    J Hered; 1984; 75(2):155-6. PubMed ID: 6201527
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2.
    Tümer Z; Tommerup N; Tønnesen T; Kreuder J; Craig IW; Horn N
    Hum Genet; 1992 Mar; 88(6):668-72. PubMed ID: 1348049
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Karyotype-phenotype correlation in females with X chromosome abnormalities.
    Kosmaidou-Aravidou Z
    Ann N Y Acad Sci; 1997 Jun; 816():373-7. PubMed ID: 9238290
    [TBL] [Abstract][Full Text] [Related]  

  • 14. X-chromosome deletions in embryo-derived (EK) cell lines associated with lack of X-chromosome inactivation.
    Rastan S; Robertson EJ
    J Embryol Exp Morphol; 1985 Dec; 90():379-88. PubMed ID: 3834036
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genetic counselling in carriers of reciprocal chromosomal translocations involving short arm of chromosome X.
    Panasiuk B; Usinskiené R; Kostyk E; Rybałko A; Stasiewicz-Jarocka B; Krzykwa B; Pieńkowska-Grela B; Kucinskas V; Michalova K; Midro AT
    Ann Genet; 2004; 47(1):11-28. PubMed ID: 15050871
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of X inactivation: loss of one X inactivation center in a case with mos45,X,-21, +der(21)t(X;21) (p21.3;p11.2)/46,X,t(X;21) (p21.3;p11.2).
    Ishikiriyama S; Iai M; Tanabe Y
    Am J Med Genet; 1993 Aug; 47(1):41-4. PubMed ID: 8368250
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Non-random X-chromosome inactivation in mouse X-autosome translocation embryos--location of the inactivation centre.
    Rastan S
    J Embryol Exp Morphol; 1983 Dec; 78():1-22. PubMed ID: 6198418
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Heteropycnosis of an underreplicating chromosome.
    Zacharias H
    Chromosoma; 1990 Apr; 99(1):24-35. PubMed ID: 2340756
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of an autoimmune serum containing antibodies against the Barr body.
    Hong B; Reeves P; Panning B; Swanson MS; Yang TP
    Proc Natl Acad Sci U S A; 2001 Jul; 98(15):8703-8. PubMed ID: 11438711
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assessment of X bends in patients with atypical X chromosome phenotypes.
    Munn CA; Wenger SL; Steele MW
    Ann Genet; 1991; 34(2):120-4. PubMed ID: 1746882
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.