Xiaofen Jin Selected Research

Tyrosine-tRNA Ligase

1/2021	Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations.
2/2016	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.

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.

Realize the full power of the drug-disease research graph!

Xiaofen Jin Research Topics

Disease

4	Leber Hereditary Optic Atrophy (Leber's Hereditary Optic Neuropathy) 01/2021 - 02/2016
3	Mitochondrial Diseases (Mitochondrial Disease) 01/2019 - 09/2014
2	Deafness (Deaf Mutism) 01/2018 - 12/2016
1	Asthma (Bronchial Asthma) 06/2021
1	Optic Nerve Diseases (Optic Neuropathy) 01/2021
1	Hypertension (High Blood Pressure) 01/2017

Drug/Important Bio-Agent (IBA)

3	Mitochondrial DNA (mtDNA)IBA 01/2019 - 02/2016
3	Transfer RNA (tRNA)IBA 01/2018 - 12/2016
2	Tyrosine-tRNA LigaseIBA 01/2021 - 02/2016
1	Formoterol Fumarate (Oxis)FDA Link 06/2021
1	Fluticasone (Cutivate)FDA LinkGeneric 06/2021
1	Fluticasone-Salmeterol Drug Combination (Advair)FDA Link 06/2021
1	Mitochondrial Proteins (Mitochondrial Protein)IBA 01/2021
1	Adenosine Triphosphatases (ATPase)IBA 01/2020
1	Electron Transport Complex I (NADH-CoQ Reductase)IBA 01/2019
1	12S ribosomal RNAIBA 01/2018
1	Adenine FDA LinkGeneric 01/2018
1	AminoglycosidesIBA 01/2018
1	Ile Transfer RNAIBA 01/2018
1	Leu Transfer RNAIBA 01/2017
1	Asp Transfer RNAIBA 12/2016
1	NucleotidesIBA 12/2016
1	Reactive Oxygen Species (Oxygen Radicals)IBA 09/2014