檢索結果 - Verity A. Letts

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  1. 1
    Isolation of the yeast structural gene for the membrane-associated enzyme phosphatidylserine synthase.

    Isolation of the yeast structural gene for the membrane-associated enzyme phosphatidylserine synthase. 由 Verity A. Letts, Lisa S. Klig, M S Bae-Lee, George Carman, Susan A. Henry

    出版 1983
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  2. 2
    Yeast mutant defective in phosphatidylcholine synthesis

    Yeast mutant defective in phosphatidylcholine synthesis 由 Miriam L. Greenberg, Lisa S. Klig, Verity A. Letts, Brenda S. Loewy, Susan A. Henry

    出版 1983
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  3. 3
    Biochemical and Biophysical Evidence for γ2 Subunit Association with Neuronal Voltage-activated Ca2+Channels

    Biochemical and Biophysical Evidence for γ2 Subunit Association with Neuronal Voltage-activated Ca2+Channels 由 Myoung‐Goo Kang, Chien‐Chang Chen, Ricardo Felix, Verity A. Letts, Wayne N. Frankel, Yasuo Mori, Kevin P. Campbell

    出版 2001
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  4. 4
    A Missense Mutation in a Highly Conserved Alternate Exon of Dynamin-1 Causes Epilepsy in Fitful Mice

    A Missense Mutation in a Highly Conserved Alternate Exon of Dynamin-1 Causes Epilepsy in Fitful Mice 由 Rebecca M. Boumil, Verity A. Letts, Monica C. Roberts, Christine Lenz, Connie L. Mahaffey, Zhongwei Zhang, Tobias Moser, Wayne N. Frankel

    出版 2010
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  5. 5
    Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4

    Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4 由 Barbara Beyer, Charlotte Deleuze, Verity A. Letts, Connie L. Mahaffey, Rebecca M. Boumil, Timothy A. Lew, John R. Huguenard, Wayne N. Frankel

    出版 2008
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  6. 6
    Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice

    Heterozygous mutations of the voltage-gated sodium channel SCN8A are associated with spike-wave discharges and absence epilepsy in mice 由 Ligia A. Papale, Barbara Beyer, Julie Miller Jones, Lisa M. Sharkey, Sérgio Tufik, Michael P. Epstein, Verity A. Letts, Miriam H. Meisler, Wayne N. Frankel, Andrew Escayg

    出版 2009
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  7. 7
    Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the<i>Cacna2d2</i>Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells

    Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the<i>Cacna2d2</i>Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells 由 J. Elaine Barclay, Nuria Balaguero, Marina Mione, Susan L. Ackerman, Verity A. Letts, Jens Brodbeck, Carles Cantı́, Alon Meir, Karen M. Page, Kenro Kusumi, Edward Perez‐Reyes, Eric S. Lander, Wayne N. Frankel, R. Mark Gardiner, Annette Dolphin, Michele Rees

    出版 2001
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  8. 8
    Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency

    Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency 由 Sarah A. Dugger, Ryan S. Dhindsa, Gabriela Louise de Almeida Sampaio, Andrew K. Ressler, Elizabeth E. Rafikian, Sabrina Petri, Verity A. Letts, Jia Jie Teoh, Junqiang Ye, Sophie Colombo, Yueqing Peng, Mu Yang, Michael J. Boland, Wayne N. Frankel, David B. Goldstein

    出版 2023
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