نتائج البحث - Thomas A. Ravenscroft

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  1. 1
    Genetics of <scp>FTLD</scp>: overview and what else we can expect from genetic studies

    Genetics of <scp>FTLD</scp>: overview and what else we can expect from genetic studies حسب Cyril Pottier, Thomas A. Ravenscroft, Mónica Sánchez-Contreras, Rosa Rademakers

    منشور في 2016
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    Revisão
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  2. 2
    <i>Drosophila</i>Voltage-Gated Sodium Channels Are Only Expressed in Active Neurons and Are Localized to Distal Axonal Initial Segment-like Domains

    <i>Drosophila</i>Voltage-Gated Sodium Channels Are Only Expressed in Active Neurons and Are Localized to Distal Axonal Initial Segment-like Domains حسب Thomas A. Ravenscroft, Jasper Janssens, Pei-Tseng Lee, Burak Tepe, Paul C. Marcogliese, Samira Makhzami, Todd C. Holmes, Stein Aerts, Hugo J. Bellen

    منشور في 2020
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    Artigo
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  3. 3
    Live imaging of the extracellular matrix with a glycan-binding fluorophore

    Live imaging of the extracellular matrix with a glycan-binding fluorophore حسب Antonio Fiore, G. Yu, Jason J. Northey, Ronak Patel, Thomas A. Ravenscroft, Richard Ikegami, Wiert Kolkman, Pratik Kumar, Tanya L. Dilan, Virginia M. S. Ruetten, Misha B. Ahrens, Hari Shroff, Shaohe Wang, Valerie M. Weaver, Kayvon Pedram

    منشور في 2025
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    Artigo
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  4. 4
    Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency

    Lipidomic and Transcriptomic Basis of Lysosomal Dysfunction in Progranulin Deficiency حسب Bret M. Evers, Carlos Rodríguez‐Navas, Rachel Tesla, Janine Prange‐Kiel, Catherine R. Wasser, Kyoung Shin Yoo, Jeffrey G. McDonald, Basar Cenik, Thomas A. Ravenscroft, Florian Plattner, Rosa Rademakers, Gang Yu, Charles L. White, Joachim Herz

    منشور في 2017
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    Artigo
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  5. 5
    Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease

    Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease حسب Cyril Pottier, Kevin F. Bieniek, Ni Cole A. Finch, Maartje van de Vorst, Matthew B. Baker, Ralph Perkersen, Patricia E. Brown, Thomas A. Ravenscroft, Marka van Blitterswijk, Alexandra M. Nicholson, Michael DeTure, David S. Knopman, Keith A. Josephs, Joseph E. Parisi, Ronald C. Petersen, Khrista Boylan, Bradley F. Boeve, Neill R. Graff‐Radford, Joris A. Veltman, Christian Gilissen, Melissa E. Murray, Dennis W. Dickson, Rosa Rademakers

    منشور في 2015
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    Artigo
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  6. 6
    TYROBP genetic variants in early-onset Alzheimer's disease

    TYROBP genetic variants in early-onset Alzheimer's disease حسب Cyril Pottier, Thomas A. Ravenscroft, Patricia H. Brown, NiCole A. Finch, Matt Baker, Meeia Parsons, Yan W. Asmann, Yingxue Ren, Elizabeth Christopher, Denise Levitch, Marka van Blitterswijk, Carlos Cruchaga, Dominique Campion, Gaël Nicolas, Anne-Claire Richard, Rita Guerreiro, José Brás, Stephan Züchner, Michael Gonzalez, Guojun Bu, Steven G. Younkin, David S. Knopman, Keith A. Josephs, Joseph E. Parisi, Ronald C. Petersen, Nilüfer Ertekin‐Taner, Neill R. Graff‐Radford, Bradley F. Boeve, Dennis W. Dickson, Rosa Rademakers

    منشور في 2016
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    Artigo
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  7. 7
    Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms

    Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms حسب Hyunglok Chung, Michael F. Wangler, Paul C. Marcogliese, Ju-Yeon Jo, Thomas A. Ravenscroft, Zhongyuan Zuo, Lita Duraine, Sina Sadeghzadeh, David Li‐Kroeger, Robert E. Schmidt, Alan Pestronk, Jill A. Rosenfeld, Lindsay C. Burrage, Mitchell J. Herndon, Shan Chen, Amelle Shillington, Marissa Vawter‐Lee, Robert J. Hopkin, Jackeline Rodriguez‐Smith, Michael Henrickson, Brendan Lee, Ann B. Moser, Richard O. Jones, Paul A. Watkins, Taekyeong Yoo, Soe Mar, Murim Choi, Robert C. Bucelli, Shinya Yamamoto, Hyun Kyoung Lee, Carlos E. Prada, Jong‐Hee Chae, Tiphanie P. Vogel, Hugo J. Bellen

    منشور في 2020
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    Artigo
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  8. 8
    <i>C9ORF72</i> repeat expansions in cases with previously identified pathogenic mutations

    <i>C9ORF72</i> repeat expansions in cases with previously identified pathogenic mutations حسب Marka van Blitterswijk, Matthew Baker, Mariely DeJesus‐Hernandez, Roberta Ghidoni, Luisa Benussi, Elizabeth Finger, Ging‐Yuek Robin Hsiung, Brendan Kelley, Melissa E. Murray, Nicola J. Rutherford, Patricia E. Brown, Thomas A. Ravenscroft, Bianca Mullen, Peter E.A. Ash, Kevin F. Bieniek, Kimmo J. Hatanpaa, Anna Karydas, Elisabeth McCarty Wood, Giovanni Coppola, Eileen H. Bigio, Carol F. Lippa, Michael J. Strong, Thomas G. Beach, David S. Knopman, Edward D. Huey, Marsel Mesulam, Thomas D. Bird, Charles L. White, Andrew Kertesz, Dan Geschwind, Vivianna M. Van Deerlin, Ronald C. Petersen, Giuliano Binetti, Bruce L. Miller, Leonard Petrucelli, Zbigniew K. Wszołek, Khrista Boylan, Neill R. Graff‐Radford, Ian R. Mackenzie, Bradley F. Boeve, Dennis W. Dickson, Rosa Rademakers

    منشور في 2013
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    Artigo
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