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Results 31-40 of 44 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2010Preferential access to genetic information from endogenous hominin ancient DNA and accurate quantitative SNP-typing via SPEXBrotherton, P.; Sanchez, J.; Cooper, A.; Endicott, P.
2007Novel high-resolution characterization of ancient DNA reveals C > U-type base modification events as the sole cause of post mortem miscoding lesionsBrotherton, P.; Endicott, P.; Sanchez, J.; Beaumont, M.; Barnett, R.; Austin, J.; Cooper, A.
2000Micronucleus induction and chromosome loss in transformed human white cells indicate clastogenic and aneugenic action of the cyanobacterial toxin, cylindrospermopsinHumpage, A.; Fenech, M.; Thomas, P.; Falconer, I.
1997Monitoring Minimal Residual Disease in Peripheral Blood in B-Lineage Acute Lymphoblastic LeukaemiaBrisco, M.; Sykes, P.; Hughes, E.; Dolman, G.; Neoh, S.; Peng, L.; Toogood, I.; Morley, A.
2008Mitochondrial genomes reveal an explosive radiation of extinct and extant bears near the Miocene-Pliocene boundaryKrause, J.; Unger, T.; Nocon, A.; Malaspinas, A.; Kolokotronis, S.; Stiller, M.; Soibelzon, L.; Spriggs, H.; Dear, P.; Briggs, A.; Bray, S.; O'Brien, S.; Rabeder, G.; Matheus, P.; Cooper, A.; Slatkin, M.; Paabo, S.; Hofreiter, M.
2008Platypus globin genes and flanking loci suggest a new insertional model for beta-globin evolution in birds and mammalsPatel, V.; Cooper, S.; Deakin, J.; Fulton, B.; Graves, T.; Warren, W.; Wilson, R.; Graves, J.
2009Genotyping human ancient mtDNA control and coding region polymorphisms with a multiplexed Single-Base-Extension assay: the singular maternal history of the Tyrolean IcemanEndicott, P.; Sanchez, J.; Pichler, I.; Brotherton, P.; Brooks, J.; Egarter-Vigl, E.; Cooper, A.; Pramstaller, P.
2007A chromosome inversion near the KIT gene and the Tobiano spotting pattern in horsesBrooks, S.; Lear, T.; Adelson, D.; Bailey, E.
2001Chicken microchromosomes are hypermethylated and can be identified by specific painting probesGrutzner, F.; Tsend-Ayush, E.; Stout, K.; Munsche, S.; Niveleau, A.; Nanda, I.; Schmid, M.; Haaf, T.
2007Array comparative genomic hybridisation analysis of boys with X-linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3Solomon, N.; Ross, S.; Forrest, S.; Thomas, P.; Morgan, T.; Belsky, J.; Hol, F.; Karnes, P.; Hopwood, N.; Myers, S.; Tan, A.; Warne, G.

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