Resultados da busca - Jingrong Tang

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  1. 1
    Neonatal Diagnosis and Treatment of Menkes Disease

    Neonatal Diagnosis and Treatment of Menkes Disease por Stephen G. Kaler, Courtney Holmes, David S. Goldstein, Jingrong Tang, Sarah C. Godwin, Anthony Donsante, Clarissa J. Liew, Susumu Satô, Nicholas J. Patronas

    Publicado em 2008
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  2. 2
    Differential Effect of Dietary Supplementation with a Soybean Oil Enriched in Oleic Acid versus Linoleic Acid on Plasma Lipids and Atherosclerosis in LDLR-Deficient Mice

    Differential Effect of Dietary Supplementation with a Soybean Oil Enriched in Oleic Acid versus Linoleic Acid on Plasma Lipids and Atherosclerosis in LDLR-Deficient Mice por Yang Zhihong, Kimball Nill, Yuki Takechi‐Haraya, Martin P. Playford, David Nguyen, Zu‐Xi Yu, Milton Pryor, Jingrong Tang, Krishna Vamsi Rojulpote, Nehal N. Mehta, Han Wen, Alan T. Remaley

    Publicado em 2022
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  3. 3
    A dual apolipoprotein C-II mimetic–apolipoprotein C-III antagonist peptide lowers plasma triglycerides

    A dual apolipoprotein C-II mimetic–apolipoprotein C-III antagonist peptide lowers plasma triglycerides por Anna Wolska, Larry Lo, Denis Sviridov, Mohsen Pourmousa, Milton Pryor, Soumitra S. Ghosh, Rahul Kakkar, Michael Davidson, Sierra R. Wilson, Richard W. Pastor, Ira J. Goldberg, Debapriya Basu, Steven K. Drake, Antony Cougnoux, Ming Jing Wu, Saskia B. Neher, Lita A. Freeman, Jingrong Tang, Marcelo Amar, Matt Devalaraja, Alan T. Remaley

    Publicado em 2020
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  4. 4
    MDS-associated mutations in germline GATA2 mutated patients with hematologic manifestations

    MDS-associated mutations in germline GATA2 mutated patients with hematologic manifestations por Lisa J. McReynolds, Yanqin Yang, Hong Yuen Wong, Jingrong Tang, Yubo Zhang, Matthew P. Mulè, Janine Daub, Cindy Palmer, Ladan Foruraghi, Qingguo Liu, Jun Zhu, Weixin Wang, Robert R. West, Marielle E. Yohe, Amy P. Hsu, Dennis D. Hickstein, Danielle M. Townsley, Steven M. Holland, Katherine R. Calvo, Christopher S. Hourigan

    Publicado em 2018
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  5. 5
    Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy

    Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy por Marina Kennerson, Garth A. Nicholson, Stephen G. Kaler, Bartosz Kowalski, Julian F. B. Mercer, Jingrong Tang, Roxana M. Llanos, Shannon Chu, Reinaldo Issao Takata, Carlos E. Speck‐Martins, Jonathan Baets, Leonardo Almeida‐Souza, Dirk Fischer, Vincent Timmerman, Philip Taylor, Steven S. Scherer, Toby A. Ferguson, Thomas D. Bird, Peter De Jonghe, Shawna Feely, Michael E. Shy, James Garbern

    Publicado em 2010
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