Name | Chen Aolong, |
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Institution | Key Laboratory of Laboratory Medicine
Ministry of Education Zhejiang Provincial Key Laboratory of Medical Genetics Department of Cell Biology and Medical Genetics College of Laboratory Medicine and Life sciences Wenzhou Medical University |
Address | , |
City | Wenzhou |
State/Province | |
Country | China |
Weblink | |
O2k-Network Lab |
Labels:
Field of research: Basic
Publications
Published | Reference | |
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Wei 2020 Hum Mutat | 2020 | Wei X, Du M, Li D, Wen S, Xie J, Li Y, Chen A, Zhang K, Xu P, Jia M, Wen C, Zhou H, Lyu J, Yang Y, Fang H (2020) Mutations in FASTKD2 are associated with mitochondrial disease with multi-OXPHOS deficiency. Hum Mutat 41:961-72. |
Han 2019 Front Physiol | 2019 | Han Y, Zhou S, Coetzee S, Chen A (2019) SIRT4 and its roles in energy and redox metabolism in health, disease and during exercise. Front Physiol 10:1006. doi: 10.3389/fphys.2019.01006 |
Chen 2018 Hum Mol Genet | 2018 | Chen A, Tiosano D, Guran T, Baris HN, Bayram Y, Mory A, Shapiro-Kulnane L, Hodges CA, Coban Akdemir Z, Turan S, Jhangiani SN, van den Akker F, Hoppel CL, Salz HK, Lupski JR, Buchner DA (2018) Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency. Hum Mol Genet 27:1913-26. |
Gispert 2009 PLoS One | 2009 | Gispert S, Ricciardi F, Kurz A, Azizov M, Hoepken HH, Becker D, Voos W, Leuner K, MΓΌller WE, Kudin AP, Kunz WS, Zimmermann A, Roeper J, Wenzel D, Jendrach M, GarcΓa-ArencΓbia M, FernΓ‘ndez-Ruiz J, Huber L, Rohrer H, Barrera M, Reichert AS, RΓΌb U, Chen A, Nussbaum RL, Auburger G (2009) Parkinson phenotype in aged PINK1-deficient mice is accompanied by progressive mitochondrial dysfunction in absence of neurodegeneration. PLoS One 4:e5777. |