Search Results - Gardner, Alison

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  1. 1
    C-Linker Accounts for Differential Sensitivity of ERG1 and ERG2 K(+) Channels to RPR260243-Induced Slow Deactivation

    C-Linker Accounts for Differential Sensitivity of ERG1 and ERG2 K(+) Channels to RPR260243-Induced Slow Deactivation by Gardner, Alison, Sanguinetti, Michael C.

    Published 2015
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  2. 2
    Comparative mortality for children at one hospital in Kenya staffed with pediatric emergency medicine specialists

    Comparative mortality for children at one hospital in Kenya staffed with pediatric emergency medicine specialists by Gardner, Alison, Fraile, Katherine, Shirk, Arianna

    Published 2020
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  3. 3
    Cooperative subunit interactions mediate fast C-type inactivation of hERG1 K(+) channels

    Cooperative subunit interactions mediate fast C-type inactivation of hERG1 K(+) channels by Wu, Wei, Gardner, Alison, Sanguinetti, Michael C

    Published 2014
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  4. 4
    Concatenated hERG1 Tetramers Reveal Stoichiometry of Altered Channel Gating by RPR-260243

    Concatenated hERG1 Tetramers Reveal Stoichiometry of Altered Channel Gating by RPR-260243 by Wu, Wei, Gardner, Alison, Sanguinetti, Michael C.

    Published 2015
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  5. 5
    The Link between Inactivation and High-Affinity Block of hERG1 Channels

    The Link between Inactivation and High-Affinity Block of hERG1 Channels by Wu, Wei, Gardner, Alison, Sanguinetti, Michael C.

    Published 2015
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  6. 6
    Structural basis of ion permeation gating in Slo2.1 K(+) channels

    Structural basis of ion permeation gating in Slo2.1 K(+) channels by Garg, Priyanka, Gardner, Alison, Garg, Vivek, Sanguinetti, Michael C.

    Published 2013
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  7. 7
    Stoichiometry of altered hERG1 channel gating by small molecule activators

    Stoichiometry of altered hERG1 channel gating by small molecule activators by Wu, Wei, Sachse, Frank B., Gardner, Alison, Sanguinetti, Michael C.

    Published 2014
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  8. 8
    Ginsenoside Rg3, a Gating Modifier of EAG Family K(+) Channels

    Ginsenoside Rg3, a Gating Modifier of EAG Family K(+) Channels by Wu, Wei, Gardner, Alison, Sachse, Frank B., Sanguinetti, Michael C.

    Published 2016
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  9. 9
    Molecular mechanisms of Slo2 K(+) channel closure

    Molecular mechanisms of Slo2 K(+) channel closure by Giese, M. Hunter, Gardner, Alison, Hansen, Angela, Sanguinetti, Michael C.

    Published 2016
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  10. 10
    Identification of a Domain That Mediates Association of Platelet-activating Factor Acetylhydrolase with High Density Lipoprotein

    Identification of a Domain That Mediates Association of Platelet-activating Factor Acetylhydrolase with High Density Lipoprotein by Gardner, Alison A., Reichert, Ethan C., Topham, Matthew K., Stafforini, Diana M.

    Published 2008
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  11. 11
    Is there a Mendelian transmission ratio distortion of the c.429_452dup(24bp) polyalanine tract ARX mutation?

    Is there a Mendelian transmission ratio distortion of the c.429_452dup(24bp) polyalanine tract ARX mutation? by Shoubridge, Cheryl, Gardner, Alison, Schwartz, Charles E, Hackett, Anna, Field, Michael, Gecz, Jozef

    Published 2012
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  12. 12
    Molecular Basis of Altered hERG1 Channel Gating Induced by Ginsenoside Rg3

    Molecular Basis of Altered hERG1 Channel Gating Induced by Ginsenoside Rg3 by Gardner, Alison, Wu, Wei, Thomson, Steven, Zangerl-Plessl, Eva-Maria, Stary-Weinzinger, Anna, Sanguinetti, Michael C.

    Published 2017
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  13. 13
    Randomized Comparison of Cooked and Noncooked Diets in Patients Undergoing Remission Induction Therapy for Acute Myeloid Leukemia

    Randomized Comparison of Cooked and Noncooked Diets in Patients Undergoing Remission Induction Therapy for Acute Myeloid Leukemia by Gardner, Alison, Mattiuzzi, Gloria, Faderl, Stefan, Borthakur, Gautam, Garcia-Manero, Guillermo, Pierce, Sherry, Brandt, Mark, Estey, Elihu

    Published 2008
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  14. 14
    Aberrant CBFA2T3B gene promoter methylation in breast tumors

    Aberrant CBFA2T3B gene promoter methylation in breast tumors by Bais, Anthony J, Gardner, Alison E, McKenzie, Olivia LD, Callen, David F, Sutherland, Grant R, Kremmidiotis, Gabriel

    Published 2004
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  15. 15
    Deficiency of phospholipase A(2) group 7 decreases intestinal polyposis and colon tumorigenesis in Apc (Min/+) mice

    Deficiency of phospholipase A(2) group 7 decreases intestinal polyposis and colon tumorigenesis in Apc (Min/+) mice by Xu, Changxin, Reichert, Ethan C., Nakano, Tomoyuki, Lohse, Mariah, Gardner, Alison A., Revelo, Mónica P., Topham, Matthew K., Stafforini, Diana M.

    Published 2013
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  16. 16
    Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism

    Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism by van Eyk, Clare L., Corbett, Mark A., Gardner, Alison, van Bon, Bregje W., Broadbent, Jessica L., Harper, Kelly, MacLennan, Alastair H., Gecz, Jozef

    Published 2018
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  17. 17
    Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females

    Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females by Jackson, Matilda R, Loring, Karagh E, Homan, Claire C, Thai, Monica HN, Määttänen, Laura, Arvio, Maria, Jarvela, Irma, Shaw, Marie, Gardner, Alison, Gecz, Jozef, Shoubridge, Cheryl

    Published 2019
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  18. 18
    The unequal impact of Covid‐19 on the lives and rights of the children of modern slavery survivors, children in exploitation and children at risk of entering exploitation

    The unequal impact of Covid‐19 on the lives and rights of the children of modern slavery survivors, children in exploitation and children at risk of entering exploitation by Jiménez, Erika, Brotherton, Vicky, Gardner, Alison, Wright, Nicola, Browne, Hannah, Esiovwa, Nancy, Dang, Minh, Wyman, Emily, Bravo‐Balsa, Liana, Lucas, Benjamin, Gul, Mohsen, Such, Elizabeth, Trodd, Zoe

    Published 2022
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  19. 19
    Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations

    Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations by Field, Michael, Scheffer, Ingrid E, Gill, Deepak, Wilson, Meredith, Christie, Louise, Shaw, Marie, Gardner, Alison, Glubb, Georgie, Hobson, Lynne, Corbett, Mark, Friend, Kathryn, Willis-Owen, Saffron, Gecz, Jozef

    Published 2012
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  20. 20
    A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24

    A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24 by Corbett, Mark A., Bahlo, Melanie, Jolly, Lachlan, Afawi, Zaid, Gardner, Alison E., Oliver, Karen L., Tan, Stanley, Coffey, Amy, Mulley, John C., Dibbens, Leanne M., Simri, Walid, Shalata, Adel, Kivity, Sara, Jackson, Graeme D., Berkovic, Samuel F., Gecz, Jozef

    Published 2010
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