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Results 421-430 of 446 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
1997A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groupsBalow Jnr., J.; Shelton, D.; Orsborn, A.; Mangelsdorf, M.; Aksentijevich, I.; Blake, T.; Sood, R.; Gardner, D.; Liu, R.; Pras, E.; Levy, E.; Centola, M.; Deng, Z.; Zaks, N.; Wood, G.; Chen, X.; Richards, N.; Shohat, M.; Livneh, A.; Pras, M.; et al.
2017The biomechanical role of the chondrocranium and sutures in a lizard craniumJones, M.A.R.C.; Gröning, F.; Dutel, H.; Sharp, A.; Fagan, M.J.; Evans, S.E.
2017Megafaunal isotopes reveal role of increased moisture on rangeland during late Pleistocene extinctionsRabanus-Wallace, M.; Wooller, M.; Zazula, G.; Shute, E.; Jahren, A.; Kosintsev, P.; Burns, J.; Breen, J.; Llamas, B.; Cooper, A.
2018Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autismVan Eyk, C.; Corbett, M.; Gardner, A.; Van Bon, B.; Broadbent, J.; Harper, K.; MacLennan, A.; Gecz, J.
1999FXY2/MID2, a gene related to the X-linked Opitz Syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubulesPerry, J.; Short, K.; Romer, J.; Swift, S.; Cox, T.; Ashworth, A.
2015Combining experimental evolution with next-generation sequencing: a powerful tool to study adaptation from standing genetic variationSchlötterer, C.; Kofler, R.; Versace, E.; Tobler, R.; Franssen, S.
2015DNA methylation abnormalities in congenital heart diseaseSerra-Juhé, C.; Cuscó, I.; Homs, A.; Flores, R.; Torán, N.; Pérez-Jurado, L.A.
2017An emerging female phenotype with loss-of-function mutations in the Aristaless-related homeodomain transcription factor ARXMattiske, T.; Moey, C.; Vissers, L.; Thorne, N.; Georgeson, P.; Bakshi, M.; Shoubridge, C.
2014Fitness valleys constrain HIV-1's adaptation to its secondary chemokine coreceptorDa Silva, J.; Wyatt, S.
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.

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