Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Justin Zhuo"'
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Akademický článek
Anaplerotic triheptanoin diet enhances mitochondrial substrate use to remodel the metabolome and improve lifespan, motor function, and sociability in MeCP2-null mice.
Autor: Min Jung Park, Susan Aja, Qun Li, Alicia L Degano, Judith Penati, Justin Zhuo, Charles R Roe, Gabriele V Ronnett
Publikováno v: PLoS ONE, Vol 9, Iss 10, p e109527 (2014)
Rett syndrome (RTT) is an autism spectrum disorder (ASD) caused by mutations in the X-linked MECP2 gene that encodes methyl-CpG binding protein 2 (MeCP2). Symptoms range in severity and include psychomotor disabilities, seizures, ataxia, and intellec
Externí odkaz: https://doaj.org/article/892c6d1a265a443aa873bd1712bfba01
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3
Development of a Preliminary Question Prompt List as a Communication Tool for Adults With Achalasia: A Modified Delphi Study
Autor: Justin Zhuo, George Triadafilopoulos, Albert J. Bredenoord, John O. Clarke, Ronnie Fass, Chandra P. Gyawali, Mary Hawn, Joo Ha Hwang, Peter J. Kahrilas, David A. Katzka, Donald Low, Benson T. Massey, Dhyanesh Patel, Roberto Penagini, Sabine Roman, Edoardo Savarino, André J. Smout, Lee Swanstrom, Roger Tatum, Marcelo F. Vela, Giovanni Zaninotto, Afrin N. Kamal
Publikováno v: Journal of clinical gastroenterology, 57(2), 159-164. Lippincott Williams and Wilkins
Background: Question prompt lists (QPLs) are structured sets of disease-specific questions that enhance patient-physician communication by encouraging patients to ask questions during consultations. Aim: The aim of this study was to develop a prelimi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f35cd99a9808cbc1e599376346ec758
https://pubmed.ncbi.nlm.nih.gov/35180150
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8
Anaplerotic Triheptanoin Diet Enhances Mitochondrial Substrate Use to Remodel the Metabolome and Improve Lifespan, Motor Function, and Sociability in MeCP2-Null Mice
Autor: Justin Zhuo, Gabriele V. Ronnett, Min Jung Park, Qun Li, Charles R. Roe, Alicia L. Degano, Susan Aja, Judith Penati
Publikováno v: PLoS ONE
PLoS ONE, Vol 9, Iss 10, p e109527 (2014)
Rett syndrome (RTT) is an autism spectrum disorder (ASD) caused by mutations in the X-linked MECP2 gene that encodes methyl-CpG binding protein 2 (MeCP2). Symptoms range in severity and include psychomotor disabilities, seizures, ataxia, and intellec
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c814f13ed53b9bce5b83a8f1059b86f
https://doi.org/10.1371/journal.pone.0109527
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