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Human Molecular Genetics|January 12, 2001
Mouse models for the Wolf-Hirschhorn deletion syndromeD Näf, L A Wilson, R A Bergstrom, et al.Neurobiology of Disease|March 25, 2014
Physiological and genetic analysis of multiple sodium channel variants in a model of genetic absence epilepsyM K Oliva, T C McGarr, B J Beyer, et al.The Journal of Clinical Endocrinology and Metabolism|April 8, 2003
Insulin and insulin propeptides at birth in offspring of diabetic mothersR S Lindsay, J D Walker, I Halsall, et al.Proceedings of the National Academy of Sciences of the United States of America|April 1, 1991
Large scale screen for transposon insertions into cloned genesB A Hamilton, M J Palazzolo, J H Chang, et al.Internal Medicine Journal|September 14, 2016
Outcomes and predictors of response from an optimised, multidisciplinary intervention for chronic fatigue statesC X Sandler, B A Hamilton, S L Horsfield, et al.British Journal of Clinical Pharmacology|May 1, 1992
A pharmacokinetic and pharmacodynamic comparison of plain and enteric-coated prednisolone tabletsC G Adair, O McCallion, J C McElnay, et al.Current Hypertension Reports|September 12, 2000
Heredity and the autonomic nervous system in human hypertensionD T O'Connor, P A Insel, M G Ziegler, et al.Human Molecular Genetics|April 6, 2000
The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5aJ M Jones, J D Huang, V Mermall, et al.Cell|September 23, 1994
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mappingJ Hästbacka, A de la Chapelle, M M Mahtani, et al.Gene|March 30, 1990
Phage lambda cDNA cloning vectors for subtractive hybridization, fusion-protein synthesis and Cre-loxP automatic plasmid subcloningM J Palazzolo, B A Hamilton, D L Ding, et al.Pageof 10