BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

131 related articles for article (PubMed ID: 1783379)

  • 1. Inactivation of the Rps4 gene on the mouse X chromosome.
    Zinn AR; Bressler SL; Beer-Romero P; Adler DA; Chapman VM; Page DC; Disteche CM
    Genomics; 1991 Dec; 11(4):1097-101. PubMed ID: 1783379
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Relationship between the monosomy X phenotype and Y-linked ribosomal protein S4 (Rps4) in several species of mammals: a molecular evolutionary analysis of Rps4 homologs.
    Omoe K; Endo A
    Genomics; 1996 Jan; 31(1):44-50. PubMed ID: 8808278
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome.
    Fisher EM; Beer-Romero P; Brown LG; Ridley A; McNeil JA; Lawrence JB; Willard HF; Bieber FR; Page DC
    Cell; 1990 Dec; 63(6):1205-18. PubMed ID: 2124517
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rps4 maps near the inactivation center on the mouse X chromosome.
    Hamvas RM; Zinn A; Keer JT; Fisher EM; Beer-Romero P; Brown SD; Page DC
    Genomics; 1992 Feb; 12(2):363-7. PubMed ID: 1740345
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression level of Rps4 mRNA in 39,X mice and 40,XX mice.
    Omoe K; Endo A
    Cytogenet Cell Genet; 1994; 67(1):52-4. PubMed ID: 8187552
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes.
    Zinn AR; Alagappan RK; Brown LG; Wool I; Page DC
    Mol Cell Biol; 1994 Apr; 14(4):2485-92. PubMed ID: 8139551
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Functional equivalence of human X- and Y-encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome.
    Watanabe M; Zinn AR; Page DC; Nishimoto T
    Nat Genet; 1993 Jul; 4(3):268-71. PubMed ID: 8358435
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Maintenance of X inactivation of the Rps4, Zfx, and Ube1 genes in a mouse in vitro system.
    Bressler SL; Lee KH; Adler DA; Chapman VM; Disteche CM
    Somat Cell Mol Genet; 1993 Jan; 19(1):29-37. PubMed ID: 7681608
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An evaluation of the inactive mouse X chromosome in somatic cell hybrids.
    Salido EC; Passage MB; Yen PH; Shapiro LJ; Mohandas TK
    Somat Cell Mol Genet; 1993 Jan; 19(1):65-71. PubMed ID: 8460399
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expression of RPS4X in fibroblasts from patients with structural aberrations of the X chromosome.
    Just W; Geerkens C; Held KR; Vogel W
    Hum Genet; 1992 May; 89(2):240-2. PubMed ID: 1587534
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ullrich-Turner syndrome is not caused by haploinsufficiency of RPS4X.
    Geerkens C; Just W; Held KR; Vogel W
    Hum Genet; 1996 Jan; 97(1):39-44. PubMed ID: 8557258
    [TBL] [Abstract][Full Text] [Related]  

  • 12. X-chromosome inactivation may explain the difference in viability of XO humans and mice.
    Ashworth A; Rastan S; Lovell-Badge R; Kay G
    Nature; 1991 May; 351(6325):406-8. PubMed ID: 2034290
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evolution of RPS4Y.
    Bergen AW; Pratt M; Mehlman PT; Goldman D
    Mol Biol Evol; 1998 Nov; 15(11):1412-9. PubMed ID: 12572605
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated.
    Jegalian K; Page DC
    Nature; 1998 Aug; 394(6695):776-80. PubMed ID: 9723615
    [TBL] [Abstract][Full Text] [Related]  

  • 15. How do genes that escape from X-chromosome inactivation contribute to Turner syndrome?
    Peeters SB; Korecki AJ; Baldry SEL; Yang C; Tosefsky K; Balaton BP; Simpson EM; Brown CJ
    Am J Med Genet C Semin Med Genet; 2019 Mar; 181(1):28-35. PubMed ID: 30779428
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of genes encoding translation initiation factor eIF-2gamma in mouse and human: sex chromosome localization, escape from X-inactivation and evolution.
    Ehrmann IE; Ellis PS; Mazeyrat S; Duthie S; Brockdorff N; Mattei MG; Gavin MA; Affara NA; Brown GM; Simpson E; Mitchell MJ; Scott DM
    Hum Mol Genet; 1998 Oct; 7(11):1725-37. PubMed ID: 9736774
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel X gene with a widely transcribed Y-linked homologue escapes X-inactivation in mouse and human.
    Agulnik AI; Mitchell MJ; Mattei MG; Borsani G; Avner PA; Lerner JL; Bishop CE
    Hum Mol Genet; 1994 Jun; 3(6):879-84. PubMed ID: 7951230
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The IL-9 receptor gene, located in the Xq/Yq pseudoautosomal region, has an autosomal origin, escapes X inactivation and is expressed from the Y.
    Vermeesch JR; Petit P; Kermouni A; Renauld JC; Van Den Berghe H; Marynen P
    Hum Mol Genet; 1997 Jan; 6(1):1-8. PubMed ID: 9002663
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous gene.
    Geerkens C; Vetter U; Just W; Fedarko NS; Fisher LW; Young MF; Termine JD; Robey PG; Wöhrle D; Vogel W
    Hum Genet; 1995 Jul; 96(1):44-52. PubMed ID: 7607653
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The murine Xe169 gene escapes X-inactivation like its human homologue.
    Wu J; Salido EC; Yen PH; Mohandas TK; Heng HH; Tsui LC; Park J; Chapman VM; Shapiro LJ
    Nat Genet; 1994 Aug; 7(4):491-6. PubMed ID: 7951318
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.