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1

Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats por Wayne N. Frankel

Publicado 2009

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2

Identification of the Mouse Neuromuscular Degeneration Gene and Mapping of a Second Site Suppressor Allele por Gregory A. Cox, Connie L. Mahaffey, Wayne N. Frankel

Publicado 1998

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Altered Calcium Channel Currents in Purkinje Cells of the Neurological Mutant Mouseleaner por Nancy M. Lorenzon, Cathleen Lutz, Wayne N. Frankel, Kurt G. Beam

Publicado 1998

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4

A Null Mutation in Inositol Polyphosphate 4-Phosphatase Type I Causes Selective Neuronal Loss in Weeble Mutant Mice por Arne Nystuen, Marie E. Legare, Leonard D. Shultz, Wayne N. Frankel

Publicado 2001

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5

Loss of MeCP2 From Forebrain Excitatory Neurons Leads to Cortical Hyperexcitation and Seizures por Wen Zhang, Matthew Peterson, Barbara Beyer, Wayne N. Frankel, Zhongwei Zhang

Publicado 2014

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6

Genetic analysis of endogenous xenotropic murine leukemia viruses: association with two common mouse mutations and the viral restriction locus Fv-1 por Wayne N. Frankel, Jonathan P. Stoye, Benjamin A. Taylor, John M. Coffin

Publicado 1989

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7

Mls-1 is encoded by the long terminal repeat open reading frame of the mouse mammary tumor provirus Mtv-7. por Ulrich Beutner, Wayne N. Frankel, M S Cote, John M. Coffin, B T Huber

Publicado 1992

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8

A linkage map of endogenous murine leukemia proviruses. por Wayne N. Frankel, Jonathan P. Stoye, Benjamin A. Taylor, John M. Coffin

Publicado 1990

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9

A Spontaneous Mutation InvolvingKcnq2(Kv7.2) Reduces M-Current Density and Spike Frequency Adaptation in Mouse CA1 Neurons por James F. Otto, Yan Yang, Wayne N. Frankel, H. Steve White, Karen S. Wilcox

Publicado 2006

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Mutation Rate and Predicted Phenotypic Target Sizes in Ethylnitrosourea-Treated Mice por Dorothy Concepcion, Kevin L. Seburn, Gen Wen, Wayne N. Frankel, Bruce A. Hamilton

Publicado 2004

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11

Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus por Nicole A. Hawkins, Melinda S. Martin, Wayne N. Frankel, Jennifer A. Kearney, Andrew Escayg

Publicado 2010

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12

Auditory brainstem responses in 10 inbred strains of mice por Xiaoming Zhou, Philip H.-S. Jen, Kevin L. Seburn, Wayne N. Frankel, Qing Yin Zheng

Publicado 2006

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13

Gait analysis detects early changes in transgenic SOD1(G93A) mice por Christine M. Wooley, Roger B. Sher, Ajit Kale, Wayne N. Frankel, Gregory A. Cox, Kevin L. Seburn

Publicado 2005

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14

Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase. por Cathy Bowes, T Li, Wayne N. Frankel, Michael Danciger, John M. Coffin, M L Applebury, Debora B. Farber

Publicado 1993

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15

Complex Seizure Disorder Caused by Brunol4 Deficiency in Mice por Yan Yang, Connie L. Mahaffey, Nathalie G. Bérubé, Terry P. Maddatu, Gregory A. Cox, Wayne N. Frankel

Publicado 2007

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16

Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2 por Jennifer A. Kearney, Yan Yang, Barbara Beyer, Sarah K. Bergren, Lieve Claes, Peter DeJonghe, Wayne N. Frankel

Publicado 2006

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17

A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice por Shinichi Tokuda, Connie L. Mahaffey, B. Monks, Christian Faulkner, Morris J. Birnbaum, Steve C. Danzer, Wayne N. Frankel

Publicado 2010

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18

Expression of the Neuronal tRNA n-Tr20 Regulates Synaptic Transmission and Seizure Susceptibility por Mridu Kapur, Archan Ganguly, Gábor Nagy, Scott I. Adamson, Jeffrey H. Chuang, Wayne N. Frankel, Susan L. Ackerman

Publicado 2020

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19

CELF4 Regulates Translation and Local Abundance of a Vast Set of mRNAs, Including Genes Associated with Regulation of Synaptic Function por Jacy L. Wagnon, Michael Briese, Wenzhi Sun, Connie L. Mahaffey, Tomaž Curk, Gregor Rot, Jernej Ule, Wayne N. Frankel

Publicado 2012

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20

A new mode of corticothalamic transmission revealed in the Gria4−/− model of absence epilepsy por Jeanne T. Paz, Astra S. Bryant, Kathy Peng, Lief E. Fenno, Ofer Yizhar, Wayne N. Frankel, Karl Deisseroth, John R. Huguenard

Publicado 2011

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Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats por Wayne N. Frankel

Identification of the Mouse Neuromuscular Degeneration Gene and Mapping of a Second Site Suppressor Allele por Gregory A. Cox, Connie L. Mahaffey, Wayne N. Frankel

Altered Calcium Channel Currents in Purkinje Cells of the Neurological Mutant Mouse<i>leaner</i> por Nancy M. Lorenzon, Cathleen Lutz, Wayne N. Frankel, Kurt G. Beam

A Null Mutation in Inositol Polyphosphate 4-Phosphatase Type I Causes Selective Neuronal Loss in Weeble Mutant Mice por Arne Nystuen, Marie E. Legare, Leonard D. Shultz, Wayne N. Frankel

Loss of MeCP2 From Forebrain Excitatory Neurons Leads to Cortical Hyperexcitation and Seizures por Wen Zhang, Matthew Peterson, Barbara Beyer, Wayne N. Frankel, Zhongwei Zhang

Genetic analysis of endogenous xenotropic murine leukemia viruses: association with two common mouse mutations and the viral restriction locus Fv-1 por Wayne N. Frankel, Jonathan P. Stoye, Benjamin A. Taylor, John M. Coffin

Mls-1 is encoded by the long terminal repeat open reading frame of the mouse mammary tumor provirus Mtv-7. por Ulrich Beutner, Wayne N. Frankel, M S Cote, John M. Coffin, B T Huber

A linkage map of endogenous murine leukemia proviruses. por Wayne N. Frankel, Jonathan P. Stoye, Benjamin A. Taylor, John M. Coffin

A Spontaneous Mutation Involving<i>Kcnq2</i>(<i>Kv7.2</i>) Reduces M-Current Density and Spike Frequency Adaptation in Mouse CA1 Neurons por James F. Otto, Yan Yang, Wayne N. Frankel, H. Steve White, Karen S. Wilcox

Mutation Rate and Predicted Phenotypic Target Sizes in Ethylnitrosourea-Treated Mice por Dorothy Concepcion, Kevin L. Seburn, Gen Wen, Wayne N. Frankel, Bruce A. Hamilton

Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus por Nicole A. Hawkins, Melinda S. Martin, Wayne N. Frankel, Jennifer A. Kearney, Andrew Escayg

Auditory brainstem responses in 10 inbred strains of mice por Xiaoming Zhou, Philip H.-S. Jen, Kevin L. Seburn, Wayne N. Frankel, Qing Yin Zheng

Gait analysis detects early changes in transgenic SOD1(G93A) mice por Christine M. Wooley, Roger B. Sher, Ajit Kale, Wayne N. Frankel, Gregory A. Cox, Kevin L. Seburn

Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase. por Cathy Bowes, T Li, Wayne N. Frankel, Michael Danciger, John M. Coffin, M L Applebury, Debora B. Farber

Complex Seizure Disorder Caused by Brunol4 Deficiency in Mice por Yan Yang, Connie L. Mahaffey, Nathalie G. Bérubé, Terry P. Maddatu, Gregory A. Cox, Wayne N. Frankel

Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2 por Jennifer A. Kearney, Yan Yang, Barbara Beyer, Sarah K. Bergren, Lieve Claes, Peter DeJonghe, Wayne N. Frankel

A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice por Shinichi Tokuda, Connie L. Mahaffey, B. Monks, Christian Faulkner, Morris J. Birnbaum, Steve C. Danzer, Wayne N. Frankel

Expression of the Neuronal tRNA n-Tr20 Regulates Synaptic Transmission and Seizure Susceptibility por Mridu Kapur, Archan Ganguly, Gábor Nagy, Scott I. Adamson, Jeffrey H. Chuang, Wayne N. Frankel, Susan L. Ackerman

CELF4 Regulates Translation and Local Abundance of a Vast Set of mRNAs, Including Genes Associated with Regulation of Synaptic Function por Jacy L. Wagnon, Michael Briese, Wenzhi Sun, Connie L. Mahaffey, Tomaž Curk, Gregor Rot, Jernej Ule, Wayne N. Frankel

A new mode of corticothalamic transmission revealed in the Gria4−/− model of absence epilepsy por Jeanne T. Paz, Astra S. Bryant, Kathy Peng, Lief E. Fenno, Ofer Yizhar, Wayne N. Frankel, Karl Deisseroth, John R. Huguenard

Resultados de búsqueda - Wayne N. Frankel

Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats por Wayne N. Frankel

Identification of the Mouse Neuromuscular Degeneration Gene and Mapping of a Second Site Suppressor Allele por Gregory A. Cox, Connie L. Mahaffey, Wayne N. Frankel

Altered Calcium Channel Currents in Purkinje Cells of the Neurological Mutant Mouse<i>leaner</i> por Nancy M. Lorenzon, Cathleen Lutz, Wayne N. Frankel, Kurt G. Beam

A Null Mutation in Inositol Polyphosphate 4-Phosphatase Type I Causes Selective Neuronal Loss in Weeble Mutant Mice por Arne Nystuen, Marie E. Legare, Leonard D. Shultz, Wayne N. Frankel

Loss of MeCP2 From Forebrain Excitatory Neurons Leads to Cortical Hyperexcitation and Seizures por Wen Zhang, Matthew Peterson, Barbara Beyer, Wayne N. Frankel, Zhongwei Zhang

Genetic analysis of endogenous xenotropic murine leukemia viruses: association with two common mouse mutations and the viral restriction locus Fv-1 por Wayne N. Frankel, Jonathan P. Stoye, Benjamin A. Taylor, John M. Coffin

Mls-1 is encoded by the long terminal repeat open reading frame of the mouse mammary tumor provirus Mtv-7. por Ulrich Beutner, Wayne N. Frankel, M S Cote, John M. Coffin, B T Huber

A linkage map of endogenous murine leukemia proviruses. por Wayne N. Frankel, Jonathan P. Stoye, Benjamin A. Taylor, John M. Coffin

A Spontaneous Mutation Involving<i>Kcnq2</i>(<i>Kv7.2</i>) Reduces M-Current Density and Spike Frequency Adaptation in Mouse CA1 Neurons por James F. Otto, Yan Yang, Wayne N. Frankel, H. Steve White, Karen S. Wilcox

Mutation Rate and Predicted Phenotypic Target Sizes in Ethylnitrosourea-Treated Mice por Dorothy Concepcion, Kevin L. Seburn, Gen Wen, Wayne N. Frankel, Bruce A. Hamilton

Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus por Nicole A. Hawkins, Melinda S. Martin, Wayne N. Frankel, Jennifer A. Kearney, Andrew Escayg

Auditory brainstem responses in 10 inbred strains of mice por Xiaoming Zhou, Philip H.-S. Jen, Kevin L. Seburn, Wayne N. Frankel, Qing Yin Zheng

Gait analysis detects early changes in transgenic SOD1(G93A) mice por Christine M. Wooley, Roger B. Sher, Ajit Kale, Wayne N. Frankel, Gregory A. Cox, Kevin L. Seburn

Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase. por Cathy Bowes, T Li, Wayne N. Frankel, Michael Danciger, John M. Coffin, M L Applebury, Debora B. Farber

Complex Seizure Disorder Caused by Brunol4 Deficiency in Mice por Yan Yang, Connie L. Mahaffey, Nathalie G. Bérubé, Terry P. Maddatu, Gregory A. Cox, Wayne N. Frankel

Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2 por Jennifer A. Kearney, Yan Yang, Barbara Beyer, Sarah K. Bergren, Lieve Claes, Peter DeJonghe, Wayne N. Frankel

A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice por Shinichi Tokuda, Connie L. Mahaffey, B. Monks, Christian Faulkner, Morris J. Birnbaum, Steve C. Danzer, Wayne N. Frankel

Expression of the Neuronal tRNA n-Tr20 Regulates Synaptic Transmission and Seizure Susceptibility por Mridu Kapur, Archan Ganguly, Gábor Nagy, Scott I. Adamson, Jeffrey H. Chuang, Wayne N. Frankel, Susan L. Ackerman

CELF4 Regulates Translation and Local Abundance of a Vast Set of mRNAs, Including Genes Associated with Regulation of Synaptic Function por Jacy L. Wagnon, Michael Briese, Wenzhi Sun, Connie L. Mahaffey, Tomaž Curk, Gregor Rot, Jernej Ule, Wayne N. Frankel

A new mode of corticothalamic transmission revealed in the Gria4−/− model of absence epilepsy por Jeanne T. Paz, Astra S. Bryant, Kathy Peng, Lief E. Fenno, Ofer Yizhar, Wayne N. Frankel, Karl Deisseroth, John R. Huguenard

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