Adelaide Research & Scholarship: Search

Search

Search:
for

Current filters:

Start a new search

Add filters:

Results/Page | Sort items by In order Authors/record

Results 71-79 of 79 (Search time: 0.004 seconds).

previous
1
...
5
6
7
8
next

Item hits:

Preview	Issue Date	Title	Author(s)
	2020	SOX3 promotes generation of committed spermatogonia in postnatal mouse testes	McAninch, D.; Mäkelä, J.-A.; La, H.M.; Hughes, J.N.; Lovell-Badge, R.; Hobbs, R.M.; Thomas, P.Q.
	2016	Mice with Sort1 deficiency display normal cognition but elevated anxiety-like behavior	Ruan, C.S.; Yang, C.R.; Li, J.Y.; Luo, H.Y.; Bobrovskaya, L.; Zhou, X.F.
	2018	A Upf3b-mutant mouse model with behavioral and neurogenesis defects	Huang, L.; Shum, E.; Jones, S.; Lou, C.-H.; Dumdie, J.; Kim, H.; Roberts, A.; Jolly, L.; Espinoza, J.; Skarbrevik, D.; Phan, M.; Cook-Andersen, H.; Swerdlow, N.; Gecz, J.; Wilkinson, M.
	2009	The ion channel TRPA1 is required for normal mechanosensation and is modulated by algesic stimuli	Brierley, S.; Hughes, P.; Page, A.; Kwan, K.; Martin, C.; O'Donnell, T.; Isaacs, N.; Harrington, A.; Adam, B.; Liebregts, T.; Holtmann, G.; Corey, D.; Rychkov, G.; Blackshaw, L.
	2008	Selective role for TRPV4 ion channels in visceral sensory pathways	Brierley, S.; Page, A.; Hughes, P.; Adam, B.; Liebregts, T.; Isaacs, N.; Holtmann, G.; Liedtke, W.; Blackshaw, L.
	2017	Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis	Hinze, S.; Jackson, M.; Lie, S.; Jolly, L.; Field, M.; Barry, S.; Harvey, R.; Shoubridge, C.
	2016	Ablation of type-1 IFN signaling in hematopoietic cells confers protection following traumatic brain injury	Karve, I.P.; Zhang, M.; Habgood, M.; Frugier, T.; Brody, K.M.; Sashindranath, M.; Joakim Ek, C.; Chappaz, S.; Kile, B.T.; Wright, D.; Wang, H.; Johnston, L.; Daglas, M.; Ates, R.C.; Medcalf, R.L.; Taylor, J.M.; Crack, P.J.
	2013	Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis	Stegeman, S.; Jolly, L.; Premarathne, S.; Gecz, J.; Richards, L.; Mackay-Sim, A.; Wood, S.; Alsina, B.
	2009	Aire-Deficient C57BL/6 Mice Mimicking the Common Human 13-Base Pair Deletion Mutation Present with Only a Mild Autoimmune Phenotype	Hubert, F.; Kinkel, S.; Crewther, P.; Cannon, P.; Webster, K.; Link, M.; Uibo, R.; O'Bryan, M.; Meager, A.; Forehan, S.; Smyth, G.; Mittaz, L.; Antonarakis, S.; Peterson, P.; Heath, W.; Scott, H.