نتائج البحث - 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. حسب Verity A. Letts, Lisa S. Klig, M S Bae-Lee, George Carman, Susan A. Henry

    منشور في 1983
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  2. 2
    Yeast mutant defective in phosphatidylcholine synthesis

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

    منشور في 1983
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    Artigo
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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 حسب Myoung‐Goo Kang, Chien‐Chang Chen, Ricardo Felix, Verity A. Letts, Wayne N. Frankel, Yasuo Mori, Kevin P. Campbell

    منشور في 2001
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    Artigo
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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 حسب Rebecca M. Boumil, Verity A. Letts, Monica C. Roberts, Christine Lenz, Connie L. Mahaffey, Zhongwei Zhang, Tobias Moser, Wayne N. Frankel

    منشور في 2010
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    Artigo
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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 حسب Barbara Beyer, Charlotte Deleuze, Verity A. Letts, Connie L. Mahaffey, Rebecca M. Boumil, Timothy A. Lew, John R. Huguenard, Wayne N. Frankel

    منشور في 2008
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    Artigo
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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 حسب 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

    منشور في 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 حسب 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

    منشور في 2001
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    Artigo
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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 حسب 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

    منشور في 2023
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    Artigo
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