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Results 1-10 of 15 (Search time: 0.005 seconds).
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PreviewIssue DateTitleAuthor(s)
1997Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2Horwitz, M.; Benson, K.; Li, F.; Wolff, J.; Leppert, M.; Hobson, L.; Mangelsdorf, M.; Yu, S.; Hewett, D.; Richards, R.; Raskind, W.
1997Chromosomal localisation of the human P2y6 purinoceptor gene and phylogenetic analysis of the P2y purinoceptor familySomers, G.; Hammet, F.; Woollatt, E.; Richards, R.; Southey, M.; Venter, D.
1997Dynamic mutation: possible mechanisms and significance in human diseaseRichards, R.; Sutherland, G.
1997Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 geneCollod-Beroud, G.; Beroud, C.; Ades, L.; Black, C.; Boxer, M.; Brock, D.; Godfrey, M.; Hayward, C.; Karttunen, L.; Milewicz, D.; Peltonen, L.; Richards, R.; Wang, M.; Junien, C.; Boileau, C.
1999Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHMFriend, K.; Crimmins, D.; Phan, T.; Sue, C.; Colley, A.; Fung, V.; Morris, J.; Sutherland, G.; Richards, R.
2013Common chromosomal fragile site FRA16D tumor suppressor WWOX gene expression and metabolic reprograming in cellsDayan, S.; O'Keefe, L.; Choo, A.; Richards, R.
2007Huntingtin-deficient zebrafish exhibit defects in iron utilization and developmentLumsden, A.; Henshall, T.; Dayan, S.; Lardelli, M.; Richards, R.
2011Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseasesLawlor, K.; O'Keefe, L.; Samaraweera, S.; van Eyk, C.; McLeod, C.; Maloney, C.; Dang, T.; Suter, C.; Richards, R.
2012Comparative toxicity of polyglutamine, polyalanine and polyleucine tracts in Drosophila models of expanded repeat diseasevan Eyk, C.; McLeod, C.; O'Keefe, L.; Richards, R.
2014Chromosomal instability causes sensitivity to metabolic stressShaukat, Z.; Liu, D.; Choo, A.; Hussain, R.; O'Keefe, L.; Richards, R.; Saint, R.; Gregory, S.