| 國立臺灣大學 |
2010 |
Gstm1, Gstp1, Prenatal Smoke Exposure, and Atopic Dermatitis
|
王怡人; 郭育良; 林天仁; 陳保中; 吳俞哖; WANG, I-JEN; GUO, YUE-LIANG; LIN, TIEN-JEN; CHEN, PAU-CHUNG; WU, YU-NIAN |
| 中國醫藥大學 |
2010-06 |
GSTM1, GSTP1, prenatal smoke exposure, and atopic dermatitis
|
王怡人; Wang I-Jen |
| 臺大學術典藏 |
2022-03-31T09:04:33Z |
GSTM1, GSTP1, prenatal smoke exposure, and atopic dermatitis
|
Wang I.-J.; YUE-LIANG GUO; Lin T.-J.; Chen P.-C.; Wu Y.-N. |
| 中國醫藥大學 |
2013-07 |
GSTM1, GSTT1, GSTP1, and GSTA1 genetic variants are not associated with coronary artery disease in Taiwan
|
(Yeh HL);(Kuo LT);宋鴻樟(Fung-Chang Sung);(Chiang CW);葉志清(Chih-Ching Yeh)* |
| 臺北醫學大學 |
2013 |
GSTM1, GSTT1, GSTP1, and GSTA1 genetic variants are not associated with coronary artery disease in Taiwan
|
HL, Yeh;LT, Kuo;FC, Sung;CW, Chiang;CC, Yeh |
| 高雄醫學大學 |
2006 |
GSTM1基因多形性變化與重型2型地中海貧血病人心臟鐵沉積有關
|
鄔康熙;張建國;彭慶添 ; Wu KH;Chang JG;Ho YJ;Wu SF;Peng CT |
| 臺大學術典藏 |
2020-10-26T11:34:25Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
JYH-MING JIMMY JUANG; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; Huang H.-C.; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C. |
| 臺大學術典藏 |
2020 |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Binda A.; Juang J.-M.J.; Antzelevitch C.; Chuang E.Y.; Rivolta I.; Lee S.-J.; Hwang J.-J.; WEN-JONE CHEN; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; Huang H.-C.; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P. |
| 臺大學術典藏 |
2020-12-28T10:52:54Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Binda A.; Juang J.-M.J.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; HUI-CHUN HUANG; Chen C.-Y.J.; Lu T.-P.; Lai L.-C.; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C. |
| 臺大學術典藏 |
2021-03-08T06:51:49Z |
GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death
|
Juang J.-M.J.;Binda A.;Lee S.-J.;Hwang J.-J.;Chen W.-J.;Liu Y.-B.;Lin L.-Y.;Yu C.-C.;Ho L.-T.;Huang H.-C.;Chen C.-Y.J.;Lu T.-P.;Liang-Chuan Lai;Yeh S.-F.S.;Lai L.-P.;Chuang E.Y.;Rivolta I.;Antzelevitch C.; Juang J.-M.J.; Binda A.; Lee S.-J.; Hwang J.-J.; Chen W.-J.; Liu Y.-B.; Lin L.-Y.; Yu C.-C.; Ho L.-T.; Huang H.-C.; Chen C.-Y.J.; Lu T.-P.; Liang-Chuan Lai; Yeh S.-F.S.; Lai L.-P.; Chuang E.Y.; Rivolta I.; Antzelevitch C. |