檢索結果 - Gregory A. Cox

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  1. 1
    Identification of the Mouse Neuromuscular Degeneration Gene and Mapping of a Second Site Suppressor Allele

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

    出版 1998
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  2. 2
    Haploinsufficiency of<i>AFG3L2</i>, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration

    Haploinsufficiency of<i>AFG3L2</i>, the Gene Responsible for Spinocerebellar Ataxia Type 28, Causes Mitochondria-Mediated Purkinje Cell Dark Degeneration 由 Francesca Maltecca, Raffaella Magnoni, Federica Cerri, Gregory A. Cox, Angelo Quattrini, Giorgio Casari

    出版 2009
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  3. 3
    Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6

    Severe disturbance in the Ca2+ signaling in astrocytes from mouse models of human infantile neuroaxonal dystrophy with mutated Pla2g6 由 Mikhail Strokin, Kevin L. Seburn, Gregory A. Cox, K. A. Martens, Georg Reiser

    出版 2012
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  4. 4
    An Active Dominant Mutation of Glycyl-tRNA Synthetase Causes Neuropathy in a Charcot-Marie-Tooth 2D Mouse Model

    An Active Dominant Mutation of Glycyl-tRNA Synthetase Causes Neuropathy in a Charcot-Marie-Tooth 2D Mouse Model 由 Kevin L. Seburn, Leslie A. Nangle, Gregory A. Cox, Paul Schimmel, Robert W. Burgess

    出版 2006
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  5. 5
    Forced expression of dystrophin deletion constructs reveals structure-function correlations.

    Forced expression of dystrophin deletion constructs reveals structure-function correlations. 由 Jill A. Rafael, Gregory A. Cox, Kathleen Corrado, Daniel Jung, Kevin P. Campbell, Jeffrey S. Chamberlain

    出版 1996
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  6. 6
    Biochemical and genetic evidence for a role of IGHMBP2 in the translational machinery

    Biochemical and genetic evidence for a role of IGHMBP2 in the translational machinery 由 Mariangels De Planell-Saguer, David G. Schroeder, Marı́a Celina Rodicio, Gregory A. Cox, Zissimos P. Mourelatos

    出版 2009
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  7. 7
    Gait analysis detects early changes in transgenic SOD1(G93A) mice

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

    出版 2005
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  8. 8
    The deacetylase HDAC4 controls myocyte enhancing factor‐2‐dependent structural gene expression in response to neural activity

    The deacetylase HDAC4 controls myocyte enhancing factor‐2‐dependent structural gene expression in response to neural activity 由 Todd J. Cohen, Tomasa Barrientos, Zachary C. Hartman, Sean M. Garvey, Gregory A. Cox, Tso‐Pang Yao

    出版 2008
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  9. 9
    Complex Seizure Disorder Caused by Brunol4 Deficiency in Mice

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

    出版 2007
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  10. 10
    Development-on-chip: <i>in vitro</i> neural tube patterning with a microfluidic device

    Development-on-chip: <i>in vitro</i> neural tube patterning with a microfluidic device 由 Christopher J. Demers, Prabakaran Soundararajan, Phaneendra Chennampally, Gregory A. Cox, James Briscoe, Scott D. Collins, R. L. Smith

    出版 2016
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  11. 11
    Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders

    Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders 由 Wen Zhang, Lifeng Zhang, Bo Liang, David G. Schroeder, Zhongwei Zhang, Gregory A. Cox, Yun Li, Da‐Ting Lin

    出版 2016
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  12. 12
    The Histone Deacetylase HDAC4 Connects Neural Activity to Muscle Transcriptional Reprogramming

    The Histone Deacetylase HDAC4 Connects Neural Activity to Muscle Transcriptional Reprogramming 由 Todd J. Cohen, David Waddell, Tomasa Barrientos, Zhonghua Lu, Guoping Feng, Gregory A. Cox, Sue C. Bodine, Tso-Pang Yao

    出版 2007
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  13. 13
    Genetic interaction between the m -AAA protease isoenzymes reveals novel roles in cerebellar degeneration

    Genetic interaction between the m -AAA protease isoenzymes reveals novel roles in cerebellar degeneration 由 Paola Martinelli, Veronica La Mattina, Andrea Bernacchia, Raffaella Magnoni, Federica Cerri, Gregory A. Cox, Angelo Quattrini, Giorgio Casari, Elena I. Rugarli

    出版 2009
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  14. 14
    MARF1 Regulates Essential Oogenic Processes in Mice

    MARF1 Regulates Essential Oogenic Processes in Mice 由 You‐Qiang Su, Koji Sugiura, Fengyun Sun, Janice K. Pendola, Gregory A. Cox, Mary Ann Handel, John C. Schimenti, John J. Eppig

    出版 2012
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  15. 15
    Corticospinal Motor Neurons Are Susceptible to Increased ER Stress and Display Profound Degeneration in the Absence of UCHL1 Function

    Corticospinal Motor Neurons Are Susceptible to Increased ER Stress and Display Profound Degeneration in the Absence of UCHL1 Function 由 Javier H. Jara, Barış Genç, Gregory A. Cox, Martha C. Bohn, Raymond P. Roos, Jeffrey D. Macklis, Emel Ulupınar, P. Hande Özdi̇nler

    出版 2015
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  16. 16
    Sodium/Hydrogen Exchanger Gene Defect in Slow-Wave Epilepsy Mutant Mice

    Sodium/Hydrogen Exchanger Gene Defect in Slow-Wave Epilepsy Mutant Mice 由 Gregory A. Cox, Cathleen Lutz, Chao-Ling Yang, Daniel Biemesderfer, Roderick T. Bronson, Audrey Qiuyan Fu, Peter S. Aronson, Jeffrey L. Noebels, Wayne N. Frankel

    出版 1997
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  17. 17
    A Direct HDAC4-MAP Kinase Crosstalk Activates Muscle Atrophy Program

    A Direct HDAC4-MAP Kinase Crosstalk Activates Muscle Atrophy Program 由 Moon-Chang Choi, Todd J. Cohen, Tomasa Barrientos, Bin Wang, Ming Li, Bryan J. Simmons, Jeong Soo Yang, Gregory A. Cox, Yingming Zhao, Tso-Pang Yao

    出版 2012
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  18. 18
    Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy

    Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy 由 Satomi Mitsuhashi, Hideyuki Hatakeyama, Minako Karahashi, Tomoko Koumura, Ikuya Nonaka, Yukiko Hayashi, S. Noguchi, Roger B. Sher, Yasuhito Nakagawa, Giovanni Manfredi, Yu‐ichi Goto, Gregory A. Cox, Ichizo Nishino

    出版 2011
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  19. 19
    A Rostrocaudal Muscular Dystrophy Caused by a Defect in Choline Kinase Beta, the First Enzyme in Phosphatidylcholine Biosynthesis

    A Rostrocaudal Muscular Dystrophy Caused by a Defect in Choline Kinase Beta, the First Enzyme in Phosphatidylcholine Biosynthesis 由 Roger B. Sher, Chieko Aoyama, Kimberly A. Huebsch, Shaonin Ji, János Kerner, Yan Yang, Wayne N. Frankel, Charles L. Hoppel, Philip A. Wood, Dennis E. Vance, Gregory A. Cox

    出版 2005
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  20. 20
    Convergence of mammalian RQC and C-end rule proteolytic pathways via alanine tailing

    Convergence of mammalian RQC and C-end rule proteolytic pathways via alanine tailing 由 Anna Thrun, Aitor Garzia, Yu Kigoshi-Tansho, Pratik Rajendra Patil, Charles S. Umbaugh, Teresa Dallinger, Jia Liu, Sylvia Kreger, Annarita Patrizi, Gregory A. Cox, Thomas Tuschl, Claudio A.P. Joazeiro

    出版 2021
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