Feifei Tao
State Council of the People's Republic of China(CN)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurological diseases and metabolism, Genetic Neurodegenerative Diseases, Peripheral Neuropathies and Disorders, Neurogenetic and Muscular Disorders Research
Most-Cited Works
- → Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder(2015)204 cited
- → Synthesis and characterization of β-cyclodextrin inclusion complexes of thymol and thyme oil for antimicrobial delivery applications(2014)168 cited
- → A novel benzo[d]imidazole derivate prevents the development of dextran sulfate sodium-induced murine experimental colitis via inhibition of NLRP3 inflammasome(2013)138 cited
- → Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia(2017)119 cited
- → A Novel Disease-Modifying Antirheumatic Drug, Iguratimod, Ameliorates Murine Arthritis by Blocking IL-17 Signaling, Distinct from Methotrexate and Leflunomide(2013)107 cited
- → Alteration of ornithine metabolism leads to dominant and recessive hereditary spastic paraplegia(2015)103 cited
- → Inhibition of Th1/Th17 responses via suppression of STAT1 and STAT3 activation contributes to the amelioration of murine experimental colitis by a natural flavonoid glucoside icariin(2012)92 cited
- → Novel monofunctional platinum (II) complex Mono-Pt induces apoptosis-independent autophagic cell death in human ovarian carcinoma cells, distinct from cisplatin(2013)90 cited
- → Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2(2018)76 cited
- → Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia(2019)60 cited