Хайлтын үр дүнгүүд - Yong-Han Hank Cheng

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  1. 1
    Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction

    Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction -н Miroslav P. Milev, Megan E. Grout, Djenann Saint‐Dic, Yong-Han Hank Cheng, Ian Glass, Christopher J. Hale, D. Hanna, Michael O. Dorschner, Keshika Prematilake, Avraham Shaag, Orly Elpeleg, Michael Sacher, Dan Doherty, Simon Edvardson

    Хэвлэсэн 2017
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    Artigo
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  2. 2
    Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish

    Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish -н Julie C. Van De Weghe, Tamara D. S. Rusterholz, Brooke Latour, Megan E. Grout, Kimberly A. Aldinger, Ranad Shaheen, Jennifer C. Dempsey, Sateesh Maddirevula, Yong-Han Hank Cheng, Ian G. Phelps, Matthias Gesemann, Himanshu Goel, Ohad S. Birk, Talal Alanzi, Rifaat Rawashdeh, Arif O. Khan, Michael J. Bamshad, Deborah A. Nickerson, Stephan C. F. Neuhauss, William B. Dobyns, Fowzan S. Alkuraya, Ronald Roepman, Ruxandra Bachmann‐Gagescu, Dan Doherty

    Хэвлэсэн 2017
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    Artigo
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  3. 3
    TDP-43 proteinopathy in ALS is triggered by loss of ASRGL1 and associated with HML-2 expression

    TDP-43 proteinopathy in ALS is triggered by loss of ASRGL1 and associated with HML-2 expression -н Marta García‐Montojo, Saeed Fathi, Cyrus Rastegar, Elena Rita Simula, Tara T. Doucet-O’Hare, Yong-Han Hank Cheng, Rachel P. M. Abrams, Nicholas Pasternack, Nasir Malik, Muzna Bachani, Brianna Disanza, Dragan Maric, Myoung‐Hwa Lee, Herui Wang, Ulisses A. Santamaria, Wenxue Li, Kevon Sampson, Ramiro Lorenzo, Ignacio E. Sánchez, Alexandre Mezghrani, Yan Li, Leonardo A. Sechi, S. Sebastian Pineda, Myriam Heiman, Manolis Kellis, Joseph P. Steiner, Avindra Nath

    Хэвлэсэн 2024
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    Artigo
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