Výsledky vyhledávání - Gardner, Alison

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females Autor 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

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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 Autor 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

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Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations Autor 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

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A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24 Autor 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

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