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Chen Aolong

From Bioblast
Name Chen Aolong,
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
Country China
O2k-Network Lab

Labels: Field of research: Basic 


Wei 2020 Hum Mutat2020Wei 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 Physiol2019Han 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 Genet2018Chen 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 One2009Gispert S, Ricciardi F, Kurz A, Azizov M, Hoepken HH, Becker D, Voos W, Leuner K, Müller WE, Kudin AP, Kunz WS, Zimmermann A, Roeper J, Wenzel D, Jendrach M, García-Arencíbia M, Fernández-Ruiz J, Huber L, Rohrer H, Barrera M, Reichert AS, Rüb 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.


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