|
|
Taiwan Academic Institutional Repository >
Browse by Author
|
"tsai ch"
Showing items 516-525 of 596 (60 Page(s) Totally)
<< < 47 48 49 50 51 52 53 54 55 56 > >>
View [10|25|50] records per page
| 國立臺灣大學 |
1999 |
Changes in the mRNA levels of delayed rectifier potassium channels in human atrial fibrillation.
|
Lai, LP; Su, MJ; Lin, JL; Lin, FY; Tsai, CH; Chen, YS; Tseng, YZ; Lien, WP; Huang, SK. |
| 國立臺灣大學 |
1999 |
Down-regulation of L-type calcium channel and sarcoplasmic reticular Ca(2+)-ATPase mRNA in human atrial fibrillation without significant change in the mRNA of ryanodine receptor, calsequestrin and phospholamban: an insight into the mechanism of atria
|
Lai, LP; Su, MJ; Lin, JL; Lin, FY; Tsai, CH; Chen, YS; Huang, SK; Tseng, YZ; Lien, WP. |
| 國立臺灣大學 |
1999 |
Measurement of funny current (I(f)) channel mRNA in human atrial tissue: correlation with left atrial filling pressure and atrial fibrillation.
|
Lai, LP; Su, MJ; Lin, JL; Tsai, CH; Lin, FY; Chen, YS; Hwang, JJ; Huang, SK; Tseng, YZ; Lien, WP. |
| 中國醫藥大學 |
1999 |
Echocardiographic (ECHO) flow pattern of patent ductus arteriosus (PDA): An indicator of indomethacin (Ind.) treatment in premature infants
|
Su, BH; Lin, HC; Peng, CT; Tsai, CH; Yeh, TF |
| 中國醫藥大學 |
1999 |
The effects of early postnatal dexamethasone (D) therapy on the blood cell count in preterm infants
|
Peng, CT; Lin, HC; Lin, YJ; Tsai, CH; Yeh, TF |
| 中國醫藥大學 |
1999 |
Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data
|
Tsai, FJ; Tsai, CH; Chang, JG; Wu, JY |
| 中國醫藥大學 |
1999 |
Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: further evidence for genetic heterogeneity
|
Tsai, FJ; Wu, JY; Tsai, CH; Chang, JG |
| 中國醫藥大學 |
1999 |
Bcl 10 is not commonly mutated in multiple primary solid tumors.
|
Chang, JG; Lee, HH; Wang, NM; Yeh, KT; Tsai, FJ; Tsai, CH |
| 中國醫藥大學 |
1999 |
A rapid and direct detection for the CYP21P/CYP21 chimeric gene in steroid 21-hydroxylase deficiency: an analysis for PCR dropout.
|
Lee, HH; Chang, JG; Tsai, CH; Chung, BC |
| 中國醫藥大學 |
1999 |
Further characterization of Wilson disease in Taiwan: identification of two novel mutations and high correlation between haplotype and mutation.
|
Wu, JY; Tsai, FJ; Lee, CC; Chang, JG; Tsai, CH |
Showing items 516-525 of 596 (60 Page(s) Totally)
<< < 47 48 49 50 51 52 53 54 55 56 > >>
View [10|25|50] records per page
|
