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研究成果 
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研究計畫
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年度
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研究名稱
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擔任
工作
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補助
金額
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補助
單位
|
|
100
|
楊建洲 建立斑馬魚為模式動物探討人類TMPRSS3基因造成聽障的成因 (100-2815-C-040-038-B)
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主持人
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47,000
|
國科會大專生計畫
|
|
100
|
100 楊建洲 Investigation of the mechanisms by which connexin26 and connexin29 mutations cause hearing loss using cellular and animal models (3/3) (98-2320-B-040-016-MY3) 主持人
|
主持人
|
1070,000
|
國科會
|
|
99
|
楊建洲 Investigation of the functional properties of connexin31 gene mutants in nonsyndromic deafness using cell model (CSMU-TSMH-099-001) 主持人
|
主持人
|
500,000
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中山醫學大學和東港安泰醫院(院際合作計畫)
|
|
99
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99 楊建洲 利用生物資訊學和斑馬魚Tol 2基因轉殖系統來尋找內耳專一表現的啟動子 (99-2815-C-040-016-B) 主持人
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主持人
|
47,000
|
國科會大專生計畫
|
|
99
|
99 楊建洲 Investigation of the mechanisms by which connexin26 and connexin29 mutations cause hearing loss using cellular and animal models (2/3) (98-2320-B-040-016-MY3) 主持人
|
主持人
|
1070,000
|
國科會
|
|
98
|
楊建洲 Study of functional properties of KCNQ4 gene mutants in nonsyndromic deafness (CSMU-TSMH-098-001) 主持人
|
主持人
|
500,000
|
中山醫學大學和東港安泰醫院(院際合作計畫)
|
|
97
|
楊建洲 Investigation of the mechanisms by which connexin26 and connexin29 mutations cause hearing loss using cellular and animal models (1/3) (98-2320-B-040-016-MY3) 主持人
|
主持人
|
1070,000
|
國科會
|
|
97
|
97 楊建洲 Study of the functional properties of Cx26 and Cx30 gene mutants in nonsyndromic deafness (CSMU-TSMH-097-001) 主持人
|
主持人
|
500,000
|
中山醫學大學和東港安泰醫院(院際合作計畫)
|
|
97
|
97 楊建洲 Study of the functional properties of TMPRSS3 gene mutants in nonsyndromic deafness (NSC97-2815-C-040-029-B) 主持人
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主持人
|
47,000
|
國科會大專生計畫
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論文發表
|
年度
|
著作
|
期刊
屬性
|
期刊最佳
百分比
|
|
100
|
Liang WG, Su CC, Nian JH, Chiang AS, Li SY*, Yang JJ* (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 61:189-197.
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SCI
|
(IF:4.312; 2010)
21.9% (16/73)
|
|
100
|
Wang WH, Liu YF, Su CC, Su MC, Li SY*, Yang JJ* (2011) A novel missense mutation in the connexin30 causes nonsyndromic hearing loss. PLoS One 6 (6): e21473. doi:10.1371/journal. pone. 0021473
|
SCI
|
(IF:4.411; 2010)
14% (12/85)
|
|
99
|
Su CC, Li SY, Su MC, Chen WC, Yang JJ* (2010) Mutation R184Q of connexin26 in hearing loss patients has a dominant-negative effect on connexin 26 and connexin 30. European Journal of Human Genetics 18:1061-1064
|
SCI
|
(IF:4.38; 2010)
19.23% (30/156)
|
|
99
|
Yang JJ, Wang WH, Lin YC, Weng HH, Yang JT, Hwang CF, Wu CM, Li SY* (2010) Prospective variants screening of connexin genes in children with hearing impairment: Genotype/ Phenotype Correlation. Human Genetics 128:303-313
|
SCI
|
(IF:5.04; 2010)
14.7% (23/156)
|
|
99
|
Yang JJ, Su MC, Chien KH, Hsin CH, Li SY* (2010) Identification of novel variants in the TMIE gene of patients with nonsyndromic hearing loss. International Journal of Pediatric Otorhinolaryngology 74:489-493
|
SCI
|
(IF:1.067; 2010)
51.2% (21/41)
|
|
99
|
Hong HM1, Yang JJ 1, Shieh JC, Lin ML, Li SY* (2010) Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss. Human Genetics 127:545-551 (1: Co-first Author)
|
SCI
|
(IF:5.047; 2010)
14.7% (23/156)
|
|
99
|
Hong HM1, Yang JJ1, Su CC, Chang JY, Li TC, Li SY* (2010) A novel mutation in the connexin 29 gene may contribute to nonsyndromic hearing loss. Human Genetics 127: 191-199 (1: Co-first Author)
|
SCI
|
(IF:5.047; 2010)
14.7% (23/156)
|
|
98
|
Su MC1, Yang JJ1, Su CC, Hsin CH, Li SY* (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 (1: Co-first Author)
|
SCI
|
(IF:1.067; 2010)
51.2% (21/41)
|
|
97
|
Yen YC1, Yang JJ1, Chou MC, Li SY* (2008) Absence of OPTINEURIN (OPTN) gene mutations in Taiwanese patients with Juvenile-Onset Open-Angle Glaucoma. Molecular Vision 14: 487-494 (1:Co-first Author)
|
SCI
|
(IF:2.511; 2010)
25.4% (14/55)
|
|
