Showing results (271-280 of 473) with videos related to
Sort By:
Pageof 48
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|June 13, 2000
Implication of screening for FMR1 and FMR2 gene mutation in individuals with nonspecific mental retardation in TaiwanC C Tzeng, P Y Tzeng, H S Sun, et al.Journal of Biomedical Materials Research|August 22, 2000
Increased corrosion resistance of stent materials by converting current surface film of polycrystalline oxide into amorphous oxideC C Shih, S J Lin, K H Chung, et al.Inorganic Chemistry|March 29, 2001
Tuning metal-to-metal charge transfer of mixed-valence complexes containing ferrocenylpyridine and rutheniumammines via solvent donicity and substituent effectsY J Chen, C H Kao, S J Lin, et al.British Journal of Cancer|November 17, 2001
Down-regulation of Fas-L in glioma cells by ribozyme reduces cell apoptosis, tumour-infiltrating cells, and liver damage but accelerates tumour formation in nude miceC C Chio, Y S Wang, Y L Chen, et al.Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|May 1, 1995
A follow-up study of genetic counseling in Down syndromeS J Lin, M C Huang, S H Chen, et al.Journal of Natural Products|February 14, 1998
In vitro biotransformations of isocupressic acid by cow rumen preparations: formation of agathic and dihydroagathic acidsS J Lin, R E Short, S P Ford, et al.Plant Physiology|August 14, 1998
Identification of a functional homolog of the yeast copper homeostasis gene ATX1 from ArabidopsisE Himelblau, H Mira, S J Lin, et al.Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|January 1, 1996
Oculomotor apraxia in a case of Gaucher's disease with homozygous T1448C mutationL P Tsai, W C Sue, W L Hwu, et al.Zhonghua Minguo Xiao Er Ke Yi Xue Hui Za Zhi [Journal]. Zhonghua Minguo Xiao Er Ke Yi Xue Hui|May 1, 1991
Niemann-Pick disease type B with ocular involvement: report of a caseF J Tsai, C T Peng, C H Tsai, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|June 1, 1997
CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defectsJ W Hou, J K Wang, W Y Tsai, et al.Pageof 48