Rezultaty - Andy Cheuk‐Him Ng

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  1. 1
    Genome-wide RNAi screen identifies ATPase inhibitory factor 1 (ATPIF1) as essential for PARK2 recruitment and mitophagy

    Genome-wide RNAi screen identifies ATPase inhibitory factor 1 (ATPIF1) as essential for PARK2 recruitment and mitophagy od Valérie Lefebvre, Qiujiang Du, Stephen Baird, Andy Cheuk-Him Ng, Mirna Nascimento, Michelangelo Campanella, Heidi M. McBride, Robert A. Screaton

    Wydane 2013
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  2. 2
    Homozygous mutations in<i>MFN2</i>cause multiple symmetric lipomatosis associated with neuropathy

    Homozygous mutations in<i>MFN2</i>cause multiple symmetric lipomatosis associated with neuropathy od Sarah L. Sawyer, Andy Cheuk‐Him Ng, A. Micheil Innes, Justin D. Wagner, David A. Dyment, Martine Tétreault, Jacek Majewski, Kym M. Boycott, Robert A. Screaton, Garth A. Nicholson

    Wydane 2015
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  3. 3
    Loss of Lkb1 in Adult β Cells Increases β Cell Mass and Enhances Glucose Tolerance in Mice

    Loss of Lkb1 in Adult β Cells Increases β Cell Mass and Enhances Glucose Tolerance in Mice od Accalia Fu, Andy Cheuk‐Him Ng, Chantal Depatie, Nadeeja Wijesekara, Ying He, Gen‐Sheng Wang, Nabeel Bardeesy, Fraser W. Scott, Rhian M. Touyz, Michael B. Wheeler, Robert A. Screaton

    Wydane 2009
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  4. 4
    Age-associated insolubility of parkin in human midbrain is linked to redox balance and sequestration of reactive dopamine metabolites

    Age-associated insolubility of parkin in human midbrain is linked to redox balance and sequestration of reactive dopamine metabolites od Jacqueline M. Tokarew, Daniel N. El-Kodsi, Nathalie A. Lengacher, Travis K. Fehr, Angela Nguyen, Bojan Shutinoski, Brian O’Nuallain, Ming Jin, Jasmine M. Khan, Andy Cheuk‐Him Ng, Juan Li, Qiubo Jiang, Mei Zhang, Liqun Wang, Rajib Sengupta, Kathryn R. Barber, An Tran, Doo Soon Im, Steve Callaghan, David S. Park, Stéphanie Zandee, Xiajun Dong, Clemens R. Scherzer, Alexandre Prat, Eve C. Tsai, Masashi Takanashi, Nobutaka Hattori, Jennifer A. Chan, Luigi Zecca, Andrew B. West, Arne Holmgren, Lawrence G. Puente, Gary S. Shaw, Gergely Tóth, John Woulfe, Peggy Taylor, Julianna J. Tomlinson, Michael G. Schlossmacher

    Wydane 2021
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  5. 5
    Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

    Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia od Ralf A. Husain, Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger, Abdelkrim Saadi, Kevin Rostásy, Florentine Radelfahr, Andrea Bevot, Marion Döbler‐Neumann, Hans Hartmann, Laurence Colleaux, Isabell Cordts, Xenia Kobeleva, Hossein Darvish, Somayeh Bakhtiari, Michael C. Kruer, Arnaud Besse, Andy Cheuk‐Him Ng, Diana Chiang, François V. Bolduc, Abbas Tafakhori, Shrikant Mane, Saghar Ghasemi Firouzabadi, Antje K. Huebner, Rebecca Buchert, Stefanie Beck‐Woedl, Amelie J. Müller, Lucia Laugwitz, Thomas Nägele, Zhao‐Qi Wang, Tim M. Strom, Marc Sturm, Thomas Meitinger, Thomas Klockgether, Olaf Rieß, Thomas Klopstock, Ulrich Brandl, Christian A. Hübner, Marcus Deschauer, Johannes A. Mayr, Penelope E. Bonnen, Ingeborg Krägeloh‐Mann, Saskia B. Wortmann, Tobias B. Haack

    Wydane 2020
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