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Molecular Medicine Reports, ISSN 1791-2997, 03/2017, Volume 15, Issue 4, pp. 1668 - 1672
Journal Article
Journal Article
International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, 08/2019, Volume 123, pp. 141 - 145
Branchio-Oto (BO) syndrome is one of the common syndromic forms of hearing loss. In this study, we aimed to characterize the clinical and genetic features of... 
Mutation | EYA1 | Branchio-Oto syndrome | Targeted next-generation sequencing | Chinese Hans | BOR SYNDROME | OTORHINOLARYNGOLOGY | SPLICE-SITE MUTATION | SIX1 | PEDIATRICS | Deafness | Medical colleges | Deaf | Genetic research | Family | Genetic aspects | Nucleotide sequencing | DNA sequencing
Journal Article
Clinical and Experimental Hypertension, ISSN 1064-1963, 08/2018, Volume 40, Issue 6, pp. 518 - 523
Here, we reported a Han Chinese essential hypertensive pedigree based on clinical hereditary and molecular data. To know the molecular basis on this family,... 
Hypertension | halopgroup | mitochondrial DNA | gene mutation | matrilineal | PHENOTYPIC MANIFESTATION | INHERITED HYPERTENSION | HYPERTROPHIC CARDIOMYOPATHY | A1555G MUTATION | DNA | PHARMACOLOGY & PHARMACY | PERIPHERAL VASCULAR DISEASE | LACTIC-ACIDOSIS | HEREDITARY OPTIC NEUROPATHY | ND4 G11778A MUTATION | TRANSFER-RNA | HAN CHINESE | Index Medicus
Journal Article
by Jiang, PP and Wang, M and Xue, L and Xiao, Y and Yu, JL and Wang, H and Yao, J and Liu, H and Peng, YY and Liu, HQ and Li, HY and Chen, Y and Guan, MX
MOLECULAR AND CELLULAR BIOLOGY, ISSN 0270-7306, 07/2016, Volume 36, Issue 14, pp. 1920 - 1930
In this report, we investigated the pathophysiology of a novel hypertension-associated mitochondrial tRNA(Ala) 5655A -> G (m.5655A -> G) mutation. The... 
MATERNALLY INHERITED HYPERTENSION | DNA MUTATION | SUPEROXIDE-PRODUCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | HAN CHINESE FAMILIES | DEAFNESS | HEREDITARY OPTIC NEUROPATHY | HEALTH | IDENTIFICATION | 4435A-GREATER-THAN-G MUTATION | CELL BIOLOGY
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 12/2015, Volume 56, Issue 1, pp. 339 - 345
Journal Article
NUCLEIC ACIDS RESEARCH, ISSN 0305-1048, 12/2016, Volume 44, Issue 22, pp. 10974 - 10985
In this report, we investigated the pathogenic mechanism underlying the deafness-associated mitochondrial(mt) tRNA(Asp) 7551A > G mutation. The m.7551A > G... 
INHERITED HEARING-LOSS | OXIDATIVE STRESS | DNA MUTATION | TRANSFER-RNA MODIFICATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRNA(SER(UCN)) GENE | NON-SYNDROMIC DEAFNESS | HAN CHINESE FAMILIES | HEREDITARY OPTIC NEUROPATHY | NONSYNDROMIC DEAFNESS | PHENOTYPIC-EXPRESSION
Journal Article
15.