Rezultati - Gregory A. Cox

Refine Results
  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 od Gregory A. Cox, Connie L. Mahaffey, Wayne N. Frankel

    Izdano 1998
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od Francesca Maltecca, Raffaella Magnoni, Federica Cerri, Gregory A. Cox, Angelo Quattrini, Giorgio Casari

    Izdano 2009
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od Mikhail Strokin, Kevin L. Seburn, Gregory A. Cox, K. A. Martens, Georg Reiser

    Izdano 2012
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od Kevin L. Seburn, Leslie A. Nangle, Gregory A. Cox, Paul Schimmel, Robert W. Burgess

    Izdano 2006
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  5. 5
    Forced expression of dystrophin deletion constructs reveals structure-function correlations.

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

    Izdano 1996
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od Mariangels De Planell-Saguer, David G. Schroeder, Marı́a Celina Rodicio, Gregory A. Cox, Zissimos P. Mourelatos

    Izdano 2009
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  7. 7
    Gait analysis detects early changes in transgenic SOD1(G93A) mice

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

    Izdano 2005
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od Todd J. Cohen, Tomasa Barrientos, Zachary C. Hartman, Sean M. Garvey, Gregory A. Cox, Tso‐Pang Yao

    Izdano 2008
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  9. 9
    Complex Seizure Disorder Caused by Brunol4 Deficiency in Mice

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

    Izdano 2007
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od Christopher J. Demers, Prabakaran Soundararajan, Phaneendra Chennampally, Gregory A. Cox, James Briscoe, Scott D. Collins, R. L. Smith

    Izdano 2016
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  11. 11
    Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders

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

    Izdano 2016
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  12. 12
    The Histone Deacetylase HDAC4 Connects Neural Activity to Muscle Transcriptional Reprogramming

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

    Izdano 2007
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od Paola Martinelli, Veronica La Mattina, Andrea Bernacchia, Raffaella Magnoni, Federica Cerri, Gregory A. Cox, Angelo Quattrini, Giorgio Casari, Elena I. Rugarli

    Izdano 2009
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  14. 14
    MARF1 Regulates Essential Oogenic Processes in Mice

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

    Izdano 2012
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od Javier H. Jara, Barış Genç, Gregory A. Cox, Martha C. Bohn, Raymond P. Roos, Jeffrey D. Macklis, Emel Ulupınar, P. Hande Özdi̇nler

    Izdano 2015
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  16. 16
    Sodium/Hydrogen Exchanger Gene Defect in Slow-Wave Epilepsy Mutant Mice

    Sodium/Hydrogen Exchanger Gene Defect in Slow-Wave Epilepsy Mutant Mice od 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

    Izdano 1997
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  17. 17
    A Direct HDAC4-MAP Kinase Crosstalk Activates Muscle Atrophy Program

    A Direct HDAC4-MAP Kinase Crosstalk Activates Muscle Atrophy Program od 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

    Izdano 2012
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  18. 18
    Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy

    Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy od 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

    Izdano 2011
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od 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

    Izdano 2005
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  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 od 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

    Izdano 2021
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:

Iskalna orodja: