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Preview	Issue Date	Title	Author(s)
	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.
	2008	An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss	Guipponi, M.; Toh, M.; Tan, J.; Park, D.; Hanson, K.; Ballana, E.; Kwong, D.; Cannon, P.; Wu, Q.; Gout, A.; Delorenzi, M.; Speed, T.; Smith, R.; Dahl, H.; Petersen, M.; Teasdale, R.; Estivill, X.; Park, W.; Scott, H.
	2008	AIRE'S CARD revealed, a new structure for the central tolerance provokes transcriptional plasticity	Ferguson, B.; Alexander, C.; Rossi, S.; Liiv, I.; Rebane, A.; Worth, C.; Wong, J.; Laan, M.; Peterson, P.; Jenkinson, E.; Anderson, G.; Scott, H.; Cooke, A.; Rich, T.
	2011	Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearing	Fasquelle, L.; Scott, H.; Lenoir, M.; Wang, J.; Rebillard, G.; Gaboyard, S.; Venteo, S.; Francois, F.; Masset-Bonnefont, A.; Antonarakis, S.; Neidhart, E.; Chabbert, C.; Puel, J.; Guipponi, M.; Delprat, B.
	2013	Tmprss3 loss of function impairs cochlear inner hair cell Kcnma1 channel membrane expression	Molina, L.; Fasquelle, L.; Nouvian, R.; Salvetat, N.; Scott, H.; Guipponi, M.; Molina, F.; Puel, J.; Delprat, B.
	2008	Autoantigen-specific interactions with CD4(+) thymocytes control mature medullary thymic epithelial cell cellularity	Irla, M.; Hugues, S.; Gill, J.; Nitta, T.; Hikosaka, Y.; Williams, I.; Hubert, F.; Scott, H.; Takahama, Y.; Hollander, G.; Reith, W.
	2012	Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature	Kazenwadel, J.; Secker, G.; Liu, Y.; Rosenfeld, J.; Wildin, R.; Cuellar-Rodriguez, J.; Hsu, A.; Dyack, S.; Fernandez, C.; Chong, C.; Babic, M.; Bardy, P.; Shimamura, A.; Zhang, M.; Walsh, T.; Holland, S.; Hickstein, D.; Horwitz, M.; Hahn, C.; Scott, H.; et al.
	2009	Hematopoietic defects in the Ts1Cje mouse model of Down syndrome	Carmichael, C.; Majewski, I.; Alexander, W.; Metcalf, D.; Hilton, D.; Hewitt, C.; Scott, H.
	2008	Integrative analysis of RUNX1 downstream pathways and target genes	Michaud, J.; Simpson, K.; Escher, R.; Buchet-Poyau, K.; Beissbarth, T.; Carmichael, C.; Ritchie, M.; Schutz, F.; Cannon, P.; Liu, M.; Shen, X.; Ito, Y.; Raskind, W.; Horwitz, M.; Osato, M.; Turner, D.; Speed, T.; Kavallaris, M.; Smyth, G.; Scott, H.
	2018	Differential effects on gene transcription and hematopoietic differentiation correlate with GATA2 mutant disease phenotypes	Chong, C.-E.; Venugopal, P.; Stokes, P.; Lee, Y.; Brautigan, P.; Yeung, D.; Babic, M.; Engler, G.; Lane, S.; Klingler-Hoffmann, M.; Matthews, J.; D'Andrea, R.; Brown, A.; Hahn, C.; Scott, H.