Dr. Shuan-Yow Li

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Interests in Research

1. Human Genetics
2. Cyto-Genetics
3. Molecular Genetics

Publications (at most 7 publications in recent 5 years)

• Wei-Guang Liang, Ching-Chyuan Su, Jhih-Hao Nian, Ann-Shyn Chiang, Shuan-Yow Li, Jiann-Jou Yang (2011) "Human connexin30.2/31.3 (GJC3) does not form functional gap junction channels but causes enhanced ATP release in HeLa cells." Cell Biochemistry and Biophysics DOI 10.1007/ s12013-011-9188-2
• Jiann-Jou Yang, Wen-Hung Wang, Yen-Chun Lin, Hsu-Huei Weng, Jen-Tsung Yang, Chung-Feng Hwang, Che-Min Wu, Shuan-Yow Li (2010) "Prospective variants screening of connexin genes in children with hearing impairment: Genotype/Phenotype Correlation" Human Genetics 128:303-313.
• Jiann-Jou Yang, Mao-Chang Su, Kuo-Hsuan Chien , Chung-Han Hsin, Shuan-Yow Li (2010) “Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss “ International Journal of Pediatric Otorhinolaryngology 74:489-493.
• Hui-Mei Hong, Jiann-Jou Yang, Jia-Ching Shieh, Mei-Ling Li, Shuan-Yow Li (2010) "Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss" Human Genetics 127:545-551.
• Wen-Hung Wang, Jiann-Jou Yang, Yen-Chun Lin, Jen-Tsung Yang, Chien-Hui Chan, Shuan-Yow Li (2010) "Identification of novel variants in the Cx29 gene of nonsyndromic hearing loss patients using buccal cells and RFLP method" Audiology and Neur-otology 15:81-87.
• Hui-Mei Hong, Jiann-Jou Yang, Ching-Chyuan Su, Juan-Yu Chang, Tung-Cheng Li, Shuan-Yow Li (2010) "A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss" Human Genetics 127:191-199.
• Mao-Chang Su, Jiann-Jou Yang, Ching-Chyuan Su, Chung-Han Hsin, and Shuan-Yow Li (2009) "Identification of novel variants in the Myosin VIIA gene of patients with nonsyndromic hearing loss from Taiwan" International Journal of Pediatric Otorhinolaryngology 73: 811-815.