1. Adelaide Research & Scholarship

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Results 181-190 of 238 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2014Mitochondrial genome sequencing in mesolithic North East Europe unearths a new sub-clade within the broadly distributed human haplogroup C1Der Sarkissian, C.; Brotherton, P.; Balanovsky, O.; Templeton, J.; Llamas, B.; Soubrier, J.; Moiseyev, V.; Khartanovich, V.; Cooper, A.; Haak, W.; Genographic Consortium,; Achilli, A.
2012Inhibition of the Pim1 oncogene results in diminished visual functionYin, J.; Shine, L.; Raycroft, F.; Deeti, S.; Reynolds, A.; Ackerman, K.; Glaviano, A.; O'Farrell, S.; O'Leary, O.; Kilty, C.; Kennedy, C.; McLoughlin, S.; Rice, M.; Russell, E.; Higgins, D.; Hyde, D.; Kennedy, B.; Thummel, R.
2014AmericaPlex26: a SNaPshot multiplex system for genotyping the main human mitochondrial founder lineages of the AmericasCoutinho, A.; Valverde, G.; Fehren-Schmitz, L.; Cooper, A.; Barreto Romero, M.; Flores Espinoza, I.; Llamas, B.; Haak, W.; Achilli, A.
2014Sustained miniaturization and anatomical innovation in the dinosaurian ancestors of birdsLee, M.; Cau, A.; Naish, D.; Dyke, G.
2014An extinct nestorid parrot (Aves, Psittaciformes, Nestoridae) from the Chatham Islands, New ZealandWood, J.; Mitchell, K.; Scofield, R.; Tennyson, A.; Fidler, A.; Wilmshurst, J.; Llamas, B.; Cooper, A.
2014SAMSN1 is a tumor suppressor gene in multiple myelomaNoll, J.; Hewett, D.; Williams, S.; Vandyke, K.; Kok, C.; To, L.; Zannettino, A.
2014A new vetulicolian from Australia and its bearing on the chordate affinities of an enigmatic Cambrian groupGarcia-Bellido, D.; Lee, M.; Edgecombe, G.; Jago, J.; Gehling, J.; Paterson, J.
2014Genetic bottlenecks in time and space: reconstructing invasions from contemporary and historical collectionsDormontt, E.; Gardner, M.; Breed, M.; Rodger, J.; Prentis, P.; Lowe, A.; Gilbert, T.
2014Insights into the Dekkera bruxellensis genomic landscape: comparative genomics reveals variations in ploidy and nutrient utilisation potential amongst wine isolatesBorneman, A.; Zeppel, R.; Chambers, P.; Curtin, C.; Bomblies, K.
2012Three novel F8 mutations in sporadic haemophilia A casesHussain, R.; Abid, N.B.; Hussain, S.; Shaukat, Z.; Altaf, M.; Altaf, S.; Niazi, G.

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