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Preview	Issue Date	Title	Author(s)
	1998	Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B	Wallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J.
	2017	Mapping complex traits in a diversity outbred f1 mouse population identifies germline modifiers of metastasis in human prostate cancer	Winter, J.; Gildea, D.; Andreas, J.; Gatti, D.; Williams, K.; Lee, M.; Hu, Y.; Zhang, S.; Mullikin, J.; Wolfsberg, T.; McDonnell, S.; Fogarty, Z.; Larson, M.; French, A.; Schaid, D.; Thibodeau, S.; Churchill, G.; Crawford, N.
	2015	HENMT1 and piRNA stability are required for adult male germ cell transposon repression and to define the spermatogenic program in the mouse	Lim, S.; Qu, Z.; Kortschak, R.; Lawrence, D.; Geoghegan, J.; Hempfling, A.; Bergmann, M.; Goodnow, C.; Ormandy, C.; Wong, L.; Mann, J.; Scott, H.; Jamsai, D.; Adelson, D.; O'Bryan, M.; Frye, M.
	2015	Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity	Moussavi Nik, S.; Newman, M.; Wilson, L.; Ebrahimie, E.; Wells, S.; Musgrave, I.; Verdile, G.; Martins, R.; Lardelli, M.
	2019	DNA hypermethylation encroachment at CpG island borders in cancer is predisposed by H3K4 monomethylation patterns	Skvortsova, K.; Masle-Farquhar, E.; Luu, P.L.; Song, J.Z.; Qu, W.; Zotenko, E.; Gould, C.M.; Du, Q.; Peters, T.J.; Colino-Sanguino, Y.; Pidsley, R.; Nair, S.S.; Khoury, A.; Smith, G.C.; Miosge, L.A.; Reed, J.H.; Kench, J.G.; Rubin, M.A.; Horvath, L.; Bogdanovic, O.; et al.
	2011	Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases	Lawlor, K.; O'Keefe, L.; Samaraweera, S.; van Eyk, C.; McLeod, C.; Maloney, C.; Dang, T.; Suter, C.; Richards, R.
	2011	Identification of SOX3 as an XX male sex reversal gene in mice and humans	Sutton, E.; Hughes, J.; White, S.; Sekido, R.; Tan, J.; Arboleda, V.; Rogers, N.; Knower, K.; Rowley, L.; Eyre, H.; Rizzoti, K.; McAninch, D.; Golcalves, J.; Slee, J.; Turbitt, E.; Bruno, D.; Bengtsson, H.; Harley, V.; Vilain, E.; Sinclair, A.; et al.
	1998	PAK3 mutation in nonsyndromic X-linked mental retardation	Allen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
	1998	The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.	Kortschak, R.; Reimann, H.; Zimmer, M.; Eyre, H.; Saint, R.; Jenne, D.