Yanyan Peng
Ultrasonic Technologies (United States)(US)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Lysosomal Storage Disorders Research, Cellular transport and secretion, High Altitude and Hypoxia, RNA modifications and cancer
Most-Cited Works
- → Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder(2015)204 cited
- → A deafness-associated tRNAHismutation alters the mitochondrial function, ROS production and membrane potential(2014)113 cited
- → The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation(2015)103 cited
- → Loss of SLC25A46 causes neurodegeneration by affecting mitochondrial dynamics and energy production in mice(2017)67 cited
- → A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function(2016)58 cited
- → HSCARG Negatively Regulates the Cellular Antiviral RIG-I Like Receptor Signaling Pathway by Inhibiting TRAF3 Ubiquitination via Recruiting OTUB1(2014)58 cited
- → miRNAs in mtDNA-less cell mitochondria(2015)57 cited
- → Whole-exome sequencing uncovers oxidoreductases DHTKD1 and OGDHL as linkers between mitochondrial dysfunction and eosinophilic esophagitis(2018)57 cited
- → Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy(2017)53 cited
- → Pathobiological Pseudohypoxia as a Putative Mechanism Underlying Myelodysplastic Syndromes(2018)52 cited