Search Results - "Myers, Cena"

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    Dynamic control of deactivation gating by a soluble amino-terminal domain in HERG K(+) channels by Wang, J, Myers, C D, Robertson, G A

    Published in The Journal of general physiology (01-06-2000)
    “…K(+) channels encoded by the human ether-à-go-go-related gene (HERG) are distinguished from most other voltage-gated K(+) channels by an unusually slow…”
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    Journal Article
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    Nucleoplasmin facilitates reprogramming and in vivo development of bovine nuclear transfer embryos by Betthauser, Jeffery M., Pfister-Genskow, Martha, Xu, Hongzhi, Golueke, Paul J., Lacson, Jenine C., Koppang, Richard W., Myers, Cena, Liu, Bing, Hoeschele, Ina, Eilertsen, Kenneth J., Leno, Gregory H.

    Published in Molecular reproduction and development (01-08-2006)
    “…Successful cloning by somatic cell nuclear transfer (NT) involves an oocyte‐driven transition in gene expression from an inherited somatic pattern, to an…”
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    Multiple Murine Double Minute Gene 2 (MDM2) Proteins Are Induced by Ultraviolet Light by Saucedo, L J, Myers, C D, Perry, M E

    Published in The Journal of biological chemistry (19-03-1999)
    “…The mdm2 ( m urine d ouble m inute 2 ) oncogene encodes several proteins, the largest of which (p90) binds to and inactivates the p53 tumor suppressor protein…”
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    Interaction with GM130 during HERG Ion Channel Trafficking by Roti, Elon C. Roti, Myers, Cena D., Ayers, Rebecca A., Boatman, Dorothy E., Delfosse, Samantha A., Chan, Edward K.L., Ackerman, Michael J., January, Craig T., Robertson, Gail A.

    Published in The Journal of biological chemistry (06-12-2002)
    “…Many mutations in the Human Ether-à-go-go-Related Gene (HERG) cause type 2 congenital long QT syndrome (LQT2) by disrupting trafficking of theHERG -encoded…”
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    Interaction with GM130 during HERG Ion Channel Trafficking. Disruption by Type 2 Congenital Long QT Syndrome Mutations by Roti, ECR, Myers, C D, Ayers, R A, Boatman, DE, Delfosse, SA, Chan, EKL, Ackerman, MJ, January, C T, Robertson, G A

    Published in The Journal of biological chemistry (06-12-2002)
    “…Many mutations in the Human Ether-a-go-go-Related Gene (HERG) cause type 2 congenital long QT syndrome (LQT2) by disrupting trafficking of the HERG-encoded…”
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    Journal Article
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