Hasil Pencarian - Craig Blackstone

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  1. 1
    A Larger BAT Improves Metabolism but Whiffs on Safety

    A Larger BAT Improves Metabolism but Whiffs on Safety oleh Craig Blackstone

    Diterbitkan 2017-10-01
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  2. 2
    Keeping in shape

    Keeping in shape oleh Craig Blackstone, William A Prinz

    Diterbitkan 2016-09-01
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  3. 3
    FAM21 directs SNX27–retromer cargoes to the plasma membrane by preventing transport to the Golgi apparatus

    FAM21 directs SNX27–retromer cargoes to the plasma membrane by preventing transport to the Golgi apparatus oleh Seongju Lee, Jaerak Chang, Craig Blackstone

    Diterbitkan 2016-03-01
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  4. 4
    Clinical Trial Designs and Measures in Hereditary Spastic Paraplegias

    Clinical Trial Designs and Measures in Hereditary Spastic Paraplegias oleh Brian Trummer, Brian Trummer, Dietrich Haubenberger, Craig Blackstone

    Diterbitkan 2018-12-01
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  5. 5
    Spastin-interacting protein NA14/SSNA1 functions in cytokinesis and axon development.

    Spastin-interacting protein NA14/SSNA1 functions in cytokinesis and axon development. oleh Uma Goyal, Benoît Renvoisé, Jaerak Chang, Craig Blackstone

    Diterbitkan 2014-01-01
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  6. 6
    Editorial: Hereditary Spastic Paraplegias: At the Crossroads of Molecular Pathways and Clinical Options

    Editorial: Hereditary Spastic Paraplegias: At the Crossroads of Molecular Pathways and Clinical Options oleh Andrea Martinuzzi, Craig Blackstone, Cahir J. O'Kane, Giovanni Stevanin

    Diterbitkan 2021-06-01
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  7. 7
    Vesicle trafficking and pathways to neurodegeneration

    Vesicle trafficking and pathways to neurodegeneration oleh Craig Blackstone, Fiona Elwood, Helene Plun-Favreau, Patrick A. Lewis

    Diterbitkan 2021-08-01
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  8. 8
    Loss of the Mitochondrial Fission GTPase Drp1 Contributes to Neurodegeneration in a <i>Drosophila</i> Model of Hereditary Spastic Paraplegia

    Loss of the Mitochondrial Fission GTPase Drp1 Contributes to Neurodegeneration in a <i>Drosophila</i> Model of Hereditary Spastic Paraplegia oleh Philippa C. Fowler, Dwayne J. Byrne, Craig Blackstone, Niamh C. O'Sullivan

    Diterbitkan 2020-09-01
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  9. 9
    Srv2 Is a Pro-fission Factor that Modulates Yeast Mitochondrial Morphology and Respiration by Regulating Actin Assembly

    Srv2 Is a Pro-fission Factor that Modulates Yeast Mitochondrial Morphology and Respiration by Regulating Actin Assembly oleh Ying-Chieh Chen, Tzu-Hao Cheng, Wei-Ling Lin, Chang-Lin Chen, Wei Yuan Yang, Craig Blackstone, Chuang-Rung Chang

    Diterbitkan 2019-01-01
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  10. 10
    Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegia

    Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegia oleh Yongchao Mou, Yi Dong, Zhenyu Chen, Kyle R. Denton, Michael O. Duff, Craig Blackstone, Su-Chun Zhang, Xue-Jun Li

    Diterbitkan 2020-12-01
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  11. 11
    Clueless/CLUH regulates mitochondrial fission by promoting recruitment of Drp1 to mitochondria

    Clueless/CLUH regulates mitochondrial fission by promoting recruitment of Drp1 to mitochondria oleh Huan Yang, Caroline Sibilla, Raymond Liu, Jina Yun, Bruce A. Hay, Craig Blackstone, David C. Chan, Robert J. Harvey, Ming Guo

    Diterbitkan 2022-03-01
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  12. 12
    Liver X receptor-agonist treatment rescues degeneration in a Drosophila model of hereditary spastic paraplegia

    Liver X receptor-agonist treatment rescues degeneration in a Drosophila model of hereditary spastic paraplegia oleh Dwayne J. Byrne, M. Elena Garcia-Pardo, Nelson B. Cole, Belguun Batnasan, Sophia Heneghan, Anood Sohail, Craig Blackstone, Niamh C. O’Sullivan

    Diterbitkan 2022-03-01
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  13. 13
    Neuronal Cx3cr1 Deficiency Protects against Amyloid β-Induced Neurotoxicity.

    Neuronal Cx3cr1 Deficiency Protects against Amyloid β-Induced Neurotoxicity. oleh Jenny Dworzak, Benoît Renvoisé, Johnny Habchi, Emma V Yates, Christophe Combadière, Tuomas P Knowles, Christopher M Dobson, Craig Blackstone, Ole Paulsen, Philip M Murphy

    Diterbitkan 2015-01-01
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  14. 14
    Chenodeoxycholic acid rescues axonal degeneration in induced pluripotent stem cell-derived neurons from spastic paraplegia type 5 and cerebrotendinous xanthomatosis patients

    Chenodeoxycholic acid rescues axonal degeneration in induced pluripotent stem cell-derived neurons from spastic paraplegia type 5 and cerebrotendinous xanthomatosis patients oleh Yongchao Mou, Ghata Nandi, Sukhada Mukte, Eric Chai, Zhenyu Chen, Jorgen E. Nielsen, Troels T. Nielsen, Chiara Criscuolo, Craig Blackstone, Matthew J. Fraidakis, Xue-Jun Li

    Diterbitkan 2023-04-01
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  15. 15
    An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15

    An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15 oleh Geert Vander Stichele, Alexandra Durr, Grace Yoon, Rebecca Schüle, Craig Blackstone, Giovanni Esposito, Connor Buffel, Inês Oliveira, Christian Freitag, Stephane van Rooijen, Stéphanie Hoffmann, Leen Thielemans, Belinda S. Cowling

    Diterbitkan 2022-03-01
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  16. 16
    A Conserved Role for Atlastin GTPases in Regulating Lipid Droplet Size

    A Conserved Role for Atlastin GTPases in Regulating Lipid Droplet Size oleh Robin W. Klemm, Justin P. Norton, Ronald A. Cole, Chen S. Li, Seong H. Park, Matthew M. Crane, Liying Li, Diana Jin, Alexandra Boye-Doe, Tina Y. Liu, Yoko Shibata, Hang Lu, Tom A. Rapoport, Robert V. Farese, Jr., Craig Blackstone, Yi Guo, Ho Yi Mak

    Diterbitkan 2013-05-01
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  17. 17
    Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases.

    Correction: Whole-Exome Sequencing Identifies Homozygous Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial -AAA Proteases. oleh Tyler Mark Pierson, David Adams, Florian Bonn, Paola Martinelli, Praveen F. Cherukuri, Jamie K. Teer, Nancy F. Hansen, Pedro Cruz, James C. Mullikin, Robert W. Blakesley, Gretchen Golas, Justin Kwan, Anthony Sandler, Karin Fuentes Fajardo, Thomas Markello, Cynthia Tifft, Craig Blackstone, Elena I. Rugarli, Thomas Langer, William A. Gahl, Camilo Toro

    Diterbitkan 2013-02-01
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  18. 18
    Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases.

    Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. oleh Tyler Mark Pierson, David Adams, Florian Bonn, Paola Martinelli, Praveen F Cherukuri, Jamie K Teer, Nancy F Hansen, Pedro Cruz, James C Mullikin For The Nisc Comparative Sequencing Program, Robert W Blakesley, Gretchen Golas, Justin Kwan, Anthony Sandler, Karin Fuentes Fajardo, Thomas Markello, Cynthia Tifft, Craig Blackstone, Elena I Rugarli, Thomas Langer, William A Gahl, Camilo Toro

    Diterbitkan 2011-10-01
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  19. 19
    AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia

    AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia oleh Salimata Diarra, Saikat Ghosh, Lassana Cissé, Thomas Coulibaly, Abdoulaye Yalcouyé, George Harmison, Salimata Diallo, Seybou H. Diallo, Oumar Coulibaly, Alice Schindler, Cheick A.K. Cissé, Alassane B. Maiga, Salia Bamba, Oumar Samassekou, Mustafa K. Khokha, Emily K. Mis, Saquib A. Lakhani, Frank X. Donovan, Steve Jacobson, Craig Blackstone, Cheick O. Guinto, Guida Landouré, Juan S. Bonifacino, Kenneth H. Fischbeck, Christopher Grunseich

    Diterbitkan 2024-08-01
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