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Pediatrics|July 2, 1999
Prevalence and parental origin in Tetralogy of Fallot associated with chromosome 22q11 microdeletionJ H Lu, M Y Chung, B Hwang, et al.Journal of Molecular Medicine (Berlin, Germany)|August 4, 2001
Absence of mutations in human ubiquitin fusion-degradation protein gene in tetralogy of FallotM Y Chung, J H Lu, Y Y Weng, et al.International Journal of Molecular Medicine|April 11, 2001
Chromosome 22q11 microdeletion in conotruncal heart defects: clinical presentation, parental origin and de novo mutationsM Y Chung, J H Lu, H P Chien, et al.Ecotoxicology and Environmental Safety|November 1, 1994
Effects of copper concentration on mineral nutrient uptake and copper accumulation in protein of copper-tolerant and nontolerant Lotus purshianus LS L Lin, L WuNature Structural Biology|October 1, 1995
A disulphide-reinforced structural scaffold shared by small proteins with diverse functionsS L Lin, R NussinovExperimental Cell Research|November 1, 1986
Disappearance of statin, a protein marker for non-proliferating and senescent cells, following serum-stimulated cell cycle entryE Wang, S L LinProtein Engineering|March 1, 1997
Three-dimensional model of sensory rhodopsin I reveals important restraints between the protein and the chromophoreS L Lin, B YanJournal of Molecular Graphics|April 1, 1996
Molecular recognition via face center representation of a molecular surfaceS L Lin, R NussinovPediatric Cardiology|May 9, 2001
Monozygotic twins with chromosome 22q11 microdeletion and discordant phenotypes in cardiovascular patterningJ H Lu, M Y Chung, B Hwang, et al.Heredity|January 11, 2003
Temporal aspects of the fine-scale genetic structure in a population of Cinnamomum insularimontanum (Lauraceae)M Y Chung, J D Nason, B K Epperson, et al.Pageof 26