|
English
|
正體中文
|
简体中文
|
Total items :0
|
|
Visitors :
53340073
Online Users :
581
Project Commissioned by the Ministry of Education Project Executed by National Taiwan University Library
|
|
|
|
Taiwan Academic Institutional Repository >
Browse by Title
|
Showing items 591806-591815 of 2348964 (234897 Page(s) Totally) << < 59176 59177 59178 59179 59180 59181 59182 59183 59184 59185 > >> View [10|25|50] records per page
| 臺大學術典藏 |
2022-01-25T07:43:15Z |
Molecular Basis of Accelerated Aging with Immune Dysfunction-Mediated Inflammation (Inflamm-Aging) in Patients with Systemic Sclerosis
|
Shen, Chieh-Yu; Lu, Cheng-Hsun; CHENG-HAN WU; Li, Ko-Jen; Kuo, Yu-Min; Hsieh, Song-Chou; Yu, Chia-Li |
| 國立臺灣大學 |
1991-12 |
Molecular Basis of an Autoantibody-Associated Restriction Fragment Length Polymorphism That Confers Susceptibility to Autoimmune Diseases
|
Olee, T.; 楊培銘; Siminovitch, K. A.; Olee, T.; Yang, Pei-Ming; Siminovitch, K. A. |
| 臺大學術典藏 |
2021-04-22T06:57:11Z |
Molecular basis of an autoantibody-associated restriction fragment length polymorphism that confers susceptibility to autoimmune diseases
|
Olee T.; PEI-MING YANG; Siminovitch K.A.; Olsen N.J.; Hillson J.; Wu J.; Kozin F.; Carson D.A.; Chen P.P. |
| 高雄醫學大學 |
2005 |
Molecular basis of diabetic nephropathy
|
辛錫璋 |
| 臺大學術典藏 |
2022-03-08T08:27:27Z |
Molecular basis of genetic variation in debrisoquin hydroxylation in Chinese subjects: Polymorphism in RFLP and DNA sequence of CYP2D6
|
Wang S.-L.; Huang J.-D.; Lai M.-D.; Liu, Biing-Hui; Lai M.-L. |
| 臺大學術典藏 |
2021-09-14T23:19:08Z |
Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variants
|
Zanetti, Alessandra; D'Avanzo, Francesca; AlSayed, Moeenaldeen; Brusius-Facchin, Ana Carolina; YIN-HSIU CHIEN; Giugliani, Roberto; Izzo, Emanuela; Kasper, David C.; Lin, Hsiang Yu; Lin, Shuan Pei; Pollard, Laura; Singh, Akashdeep; Tonin, Rodolfo; Wood, Tim; Morrone, Amelia; Tomanin, Rosella |
| 臺大學術典藏 |
2022-03-28T02:45:59Z |
Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variants
|
Zanetti A.; D'Avanzo F.; AlSayed M.; Brusius-Facchin A.C.; YIN-HSIU CHIEN; Giugliani R.; Izzo E.; Kasper D.C.; Lin H.-Y.; Lin S.-P.; Pollard L.; Singh A.; Tonin R.; Wood T.; Morrone A.; Tomanin R. |
| 臺大學術典藏 |
2020-01-22T07:46:19Z |
Molecular basis of the adult i phenotype and the gene responsible for the expression of the human blood group I antigen
|
Yu L.-C.; Twu Y.-C.; Chang C.-Y.; Lin M.; LUNG-CHIH YU |
| 國立臺灣大學 |
2001-12 |
Molecular basis of the adult i phenotype and the gene responsible for the expression of the human blood group I antigen.
|
Yu, LC; Twu, YC; Chang, CY; Lin, M |
| 臺大學術典藏 |
2020-01-22T07:46:19Z |
Molecular basis of the Kell-null phenotype: A mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigens
|
Yu L.-C.; Twu Y.-C.; Chang C.-Y.; Lin M.; LUNG-CHIH YU |
Showing items 591806-591815 of 2348964 (234897 Page(s) Totally) << < 59176 59177 59178 59179 59180 59181 59182 59183 59184 59185 > >> View [10|25|50] records per page
|