Showing results (41-50 of 848) with videos related to

Sort By:
Pageof 85
Human Genetics|May 1, 1989
Centromeric alpha satellite DNA amplification and translocation in an unusually large chromosome 14p+ variantS Dale, E Earle, L Voullaire, et al.
Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)|April 1, 1997
Analysis of the possible protective role of metallothionein in streptozotocin-induced diabetes using metallothionein-null miceM D Apostolova, K H Choo, A E Michalska, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 1998
Targeted disruption of mouse centromere protein C gene leads to mitotic disarray and early embryo deathP Kalitsis, K J Fowler, E Earle, et al.
Nature|September 9, 1982
Molecular cloning of the gene for human anti-haemophilic factor IXK H Choo, K G Gould, D J Rees, et al.
Nucleic Acids Research|February 25, 1988
Homologous alpha satellite sequences on human acrocentric chromosomes with selectivity for chromosomes 13, 14 and 21: implications for recombination between nonhomologues and Robertsonian translocationsK H Choo, B Vissel, R Brown, et al.
The Biochemical Journal|July 1, 1981
Molecular and immunological comparison of human dihydropteridine reductase in liver, cultured fibroblasts and continuous lymphoid cellsF A Firgaira, K H Choo, R G Cotton, et al.
The Biochemical Journal|September 15, 1981
Heterogeneity of the molecular defect in human dihydropteridine reductase deficiencyF A Firgaira, K H Choo, R G Cotton, et al.
Human Genetics|December 29, 2000
Components of the human spindle checkpoint control mechanism localize specifically to the active centromere on dicentric chromosomesR Saffery, D V Irvine, B Griffiths, et al.
Water Science and Technology : a Journal of the International Association on Water Pollution Research|July 12, 2005
Removal of manganese from water using combined chelation/membrane separation systemsS C Han, K H Choo, S J Choi, et al.
The Biochemical Journal|August 1, 1979
Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuriaK H Choo, R G Cotton, D M Danks, et al.
Pageof 85