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Min-xin Guan Selected Research

Mitochondrial Diseases (Mitochondrial Disease)

6/2012[Mitochondrial genetics and human essential hypertension].
10/2011[The mitochondrial tRNA(Thr) A15951G mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families].

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Min-xin Guan Research Topics

Disease

3Deafness (Deaf Mutism)
12/2013 - 08/2012
2Hearing Loss (Hearing Impairment)
12/2013 - 08/2012
2Nonsyndromic Deafness
08/2012 - 08/2011
2Mitochondrial Diseases (Mitochondrial Disease)
06/2012 - 10/2011
2Vision Disorders (Hemeralopia)
10/2011 - 02/2008
1Essential Hypertension
06/2012
1Hypertension (High Blood Pressure)
06/2012
1Leber Hereditary Optic Atrophy (Leber's Hereditary Optic Neuropathy)
10/2011

Drug/Important Bio-Agent (IBA)

5Mitochondrial DNA (mtDNA)IBA
12/2013 - 02/2008
2DNA (Deoxyribonucleic Acid)IBA
12/2013 - 08/2011
212S ribosomal RNAIBA
08/2012 - 08/2011
2AminoglycosidesIBA
08/2012 - 08/2011
1Asp Transfer RNAIBA
12/2013
1Transfer RNA (tRNA)IBA
10/2011
1Thr Transfer RNAIBA
10/2011
1ConnexinsIBA
08/2011