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Journal of Molecular Biology|January 22, 2002
Mutational analysis of the transferrin receptor reveals overlapping HFE and transferrin binding sitesA P West, A M Giannetti, A B Herr, et al.American Journal of Reproductive Immunology (New York, N.Y. : 1989)|March 1, 1993
Treatment of recurrent spontaneous abortion by immunization with paternal lymphocytes: results of a controlled trialP A Gatenby, K Cameron, R J Simes, et al.Journal of Medicinal Chemistry|January 21, 1994
Tetrapeptide CCK agonists: structure-activity studies on modifications at the N-terminusR L Elliott, H Kopecka, M J Bennett, et al.Journal of Inherited Metabolic Disease|February 22, 2000
Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disordersJ J Shen, D Matern, D S Millington, et al.British Journal of Obstetrics and Gynaecology|February 1, 1979
Antenatal screening in Oxford for fetal neural tube defectsN J Wald, H S Cuckle, J Boreham, et al.Journal of Medicinal Chemistry|May 27, 1994
CCK-A-selective tetrapeptides containing lys(N epsilon)-amide residues: favorable in vivo and in vitro effects of N-methylation at the aspartyl residueM J Bennett, A L Nikkel, B R Bianchi, et al.Biochemical and Molecular Medicine|December 1, 1996
Toxicity of cationic lipid-ribozyme complexes in human prostate tumor cells can mimic ribozyme activityS J Freedland, R W Malone, H M Borchers, et al.Journal of Medicinal Chemistry|August 7, 1992
Synthesis and biological activity of CCK heptapeptide analogues. Effects of conformational constraints and standard modifications on receptor subtype selectivity, functional activity in vitro, and appetite suppression in vivoM W Holladay, M J Bennett, M D Tufano, et al.Journal of Lipid Research|July 7, 2001
Molecular characterization of L-CPT I deficiency in six patients: insights into function of the native enzymeN F Brown, R S Mullur, I Subramanian, et al.Human Molecular Genetics|May 16, 1998
Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, together conferring susceptibility to ethylmalonic aciduriaN Gregersen, V S Winter, M J Corydon, et al.Pageof 25