Search Results - "Gapp, K."

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  1. 1

    Epigenetic germline inheritance in mammals: looking to the past to understand the future by Gapp, K., Bohacek, J.

    Published in Genes, brain and behavior (01-03-2018)
    “…Life experiences can induce epigenetic changes in mammalian germ cells, which can influence the developmental trajectory of the offspring and impact health and…”
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    Journal Article
  2. 2

    Alterations in sperm long RNA contribute to the epigenetic inheritance of the effects of postnatal trauma by Gapp, K., van Steenwyk, G., Germain, P. L., Matsushima, W., Rudolph, K. L. M., Manuella, F., Roszkowski, M., Vernaz, G., Ghosh, T., Pelczar, P., Mansuy, I. M., Miska, E. A.

    Published in Molecular psychiatry (01-09-2020)
    “…Psychiatric diseases have a strong heritable component known to not be restricted to DNA sequence-based genetic inheritance alone but to also involve…”
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  3. 3

    Pathological brain plasticity and cognition in the offspring of males subjected to postnatal traumatic stress by Bohacek, J, Farinelli, M, Mirante, O, Steiner, G, Gapp, K, Coiret, G, Ebeling, M, Durán-Pacheco, G, Iniguez, A L, Manuella, F, Moreau, J-L, Mansuy, I M

    Published in Molecular psychiatry (01-05-2015)
    “…Traumatic stress in early-life increases the risk for cognitive and neuropsychiatric disorders later in life. Such early stress can also impact the progeny…”
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  4. 4

    Epigenetic regulation in neurodevelopment and neurodegenerative diseases by Gapp, K, Woldemichael, B.T, Bohacek, J, Mansuy, I.M

    Published in Neuroscience (04-04-2014)
    “…Highlights ► The involvement of epigenetic processes in neurodevelopment. ► Their contribution to neurodegenerative diseases. ► Their study in animal models…”
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  5. 5

    Advancing BSNs by 2020: Innovative Educational Progression for Success by Roberts, Melina S., Gapp, DeAnna K., Burns-Coral, Mary, Greaves, Valerie D., Williams, Michael L.

    Published in Nursing education perspectives (01-09-2020)
    “…Abstract As we approach 2020, with limited time to meet the Institute of Medicine goal of 80 percent baccalaureate in nursing by 2020, there is a need for…”
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  6. 6
  7. 7

    Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function by Maclachlan, Annabel, Dolan, Gerry, Grimley, Charlotte, Watson, Steve P., Morgan, Neil V., on behalf of the UK GAPP Study Group

    Published in Platelets (Edinburgh) (18-08-2017)
    “…Here, we describe a mother and son with a lifelong bleeding tendency and posttraumatic bleeding who were recruited to the UK Genotyping and Phenotyping of…”
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