Search Results - "Swaggart, Kayleigh A."

  • Showing 1 - 12 results of 12
Refine Results
  1. 1
  2. 2

    Making a Genetic Diagnosis in a Level IV Neonatal Intensive Care Unit Population: Who, When, How, and at What Cost? by Swaggart, Kayleigh A., Swarr, Daniel T., Tolusso, Leandra K., He, Hua, Dawson, D. Brian, Suhrie, Kristen R.

    Published in The Journal of pediatrics (01-10-2019)
    “…To investigate the prevalence of genetic disease and its economic impact in a level IV neonatal intensive care unit (NICU) by identifying and describing…”
    Get full text
    Journal Article
  3. 3
  4. 4

    Modifiers of heart and muscle function: where genetics meets physiology by Swaggart, Kayleigh A., McNally, Elizabeth M.

    Published in Experimental physiology (01-04-2014)
    “…New Findings What is the topic of this review? Genetic modifiers act on many different physiological aspects of muscle disease. Understanding and identifying…”
    Get full text
    Journal Article
  5. 5

    Myoferlin is required for insulin-like growth factor response and muscle growth by Demonbreun, Alexis R, Posey, Avery D, Heretis, Konstantina, Swaggart, Kayleigh A, Earley, Judy U, Pytel, Peter, McNally, Elizabeth M

    Published in The FASEB journal (01-04-2010)
    “…Insulin-like growth factor (IGF) is a potent stimulus of muscle growth. Myoferlin is a membrane-associated protein important for muscle development and…”
    Get full text
    Journal Article
  6. 6

    The superhealing MRL background improves muscular dystrophy by Heydemann, Ahlke, Swaggart, Kayleigh A, Kim, Gene H, Holley-Cuthrell, Jenan, Hadhazy, Michele, McNally, Elizabeth M

    Published in Skeletal muscle (05-12-2012)
    “…Mice from the MRL or "superhealing" strain have enhanced repair after acute injury to the skin, cornea, and heart. We now tested an admixture of the MRL genome…”
    Get full text
    Journal Article
  7. 7

    Detecting endogenous retrovirus-driven tissue-specific gene transcription by Pavlicev, Mihaela, Hiratsuka, Kaori, Swaggart, Kayleigh A, Dunn, Caitlin, Muglia, Louis

    Published in Genome biology and evolution (01-04-2015)
    “…Transposable elements (TEs) comprise approximately half of the human genome, and several independent lines of investigation have demonstrated their role in…”
    Get full text
    Journal Article
  8. 8

    Dusp6 is a genetic modifier of growth through enhanced ERK activity by Vo, Andy H, Swaggart, Kayleigh A, Woo, Anna, Gao, Quan Q, Demonbreun, Alexis R, Fallon, Katherine S, Quattrocelli, Mattia, Hadhazy, Michele, Page, Patrick G T, Chen, Zugen, Eskin, Ascia, Squire, Kevin, Nelson, Stanley F, McNally, Elizabeth M

    Published in Human molecular genetics (15-01-2019)
    “…Abstract Like other single-gene disorders, muscular dystrophy displays a range of phenotypic heterogeneity even with the same primary mutation. Identifying…”
    Get full text
    Journal Article
  9. 9

    Muscle hypertrophy induced by myostatin inhibition accelerates degeneration in dysferlinopathy by Lee, Yun-Sil, Lehar, Adam, Sebald, Suzanne, Liu, Min, Swaggart, Kayleigh A, Talbot, Jr, C Conover, Pytel, Peter, Barton, Elisabeth R, McNally, Elizabeth M, Lee, Se-Jin

    Published in Human molecular genetics (15-10-2015)
    “…Myostatin is a secreted signaling molecule that normally acts to limit muscle growth. As a result, there is extensive effort directed at developing drugs…”
    Get full text
    Journal Article
  10. 10

    Genomics of preterm birth by Swaggart, Kayleigh A, Pavlicev, Mihaela, Muglia, Louis J

    “…The molecular mechanisms controlling human birth timing at term, or resulting in preterm birth, have been the focus of considerable investigation, but limited…”
    Get full text
    Journal Article
  11. 11

    Distinct genetic regions modify specific muscle groups in muscular dystrophy by Swaggart, Kayleigh A, Heydemann, Ahlke, Palmer, Abraham A, McNally, Elizabeth M

    Published in Physiological genomics (07-01-2011)
    “…Phenotypic expression in the muscular dystrophies is variable, even with the identical mutation, providing strong evidence that genetic modifiers influence…”
    Get full text
    Journal Article
  12. 12

    Expression and Nucleotide Diversity of the Maize RIK Gene by Buckner, Brent, Swaggart, Kayleigh A., Wong, Cheryl C., Smith, Heath A., Aurand, Kelsey M., Scanlon, Michael J., Schnable, Patrick S., Janick-Buckner, Diane

    Published in The Journal of heredity (01-07-2008)
    “…The K homology (KH) domain is a conserved sequence present in a wide variety of RNA-binding proteins. The rough sheath2–interacting KH domain (RIK) protein of…”
    Get full text
    Journal Article