• /
  • Publications

Keyword Connections

Connections to Genes, X-Linked are shown below. Double-click or tap a node for more information.

Please note that publication matches are limited to 40 in this view. If you expected more, please view all publication matches for Genes, X-Linked.


Members

  • No matching connections

Resources

  • No matching connections

Communities

  • No matching connections

Publications

  • Landscape of X chromosome inactivation across human tissues.
    Tukiainen T, Villani AC, Yen A, Rivas MA, Marshall JL, Satija R, Aguirre M, Gauthier L, Fleharty M, Kirby A, Cummings BB, Castel SE, Karczewski KJ, Aguet F, Byrnes A, GTEx Consortium, Laboratory, Data Analysis &Coordinating Center (LDACC)—Analysis Working Group, Statistical Methods groups—Analysis Working Group, Enhancing GTEx (eGTEx) groups, NIH Common Fund, NIH/NCI, NIH/NHGRI, NIH/NIMH, NIH/NIDA, Biospecimen Collection Source Site—NDRI, Biospecimen Collection Source Site—RPCI, Biospecimen Core Resource—VARI, Brain Bank Repository—University of Miami Brain Endowment Bank, Leidos Biomedical—Project Management, ELSI Study, Genome Browser Data Integration &Visualization—EBI, Genome Browser Data Integration &Visualization—UCSC Genomics Institute, University of California Santa Cruz, Lappalainen T, Regev A, Ardlie KG, Hacohen N, MacArthur DG
    (2017) Nature 550: 244-248
  • A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.
    Celestino-Soper PB, Violante S, Crawford EL, Luo R, Lionel AC, Delaby E, Cai G, Sadikovic B, Lee K, Lo C, Gao K, Person RE, Moss TJ, German JR, Huang N, Shinawi M, Treadwell-Deering D, Szatmari P, Roberts W, Fernandez B, Schroer RJ, Stevenson RE, Buxbaum JD, Betancur C, Scherer SW, Sanders SJ, Geschwind DH, Sutcliffe JS, Hurles ME, Wanders RJ, Shaw CA, Leal SM, Cook EH, Goin-Kochel RP, Vaz FM, Beaudet AL
    (2012) Proc Natl Acad Sci U S A 109: 7974-81
  • Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regeneration.
    Melcon G, Kozlov S, Cutler DA, Sullivan T, Hernandez L, Zhao P, Mitchell S, Nader G, Bakay M, Rottman JN, Hoffman EP, Stewart CL
    (2006) Hum Mol Genet 15: 637-51
  • Comprehensive evaluation of the contribution of X chromosome genes to platinum sensitivity.
    Gamazon ER, Im HK, O'Donnell PH, Ziliak D, Stark AL, Cox NJ, Dolan ME, Huang RS
    (2011) Mol Cancer Ther 10: 472-80
Hints: (1) double-click or double-tap to navigate to a node. (2) Grab a node and move it to arrange the graph.