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PreviewIssue DateTitleAuthor(s)
2017NAD deficiency, congenital malformations, and niacin supplementationShi, H.; Enriquez, A.; Rapadas, M.; Martin, E.; Wang, R.; Moreau, J.; Lim, C.; Szot, J.; Ip, E.; Hughes, J.; Sugimoto, K.; Humphreys, D.; McInerney-Leo, A.; Leo, P.; Maghzal, G.; Halliday, J.; Smith, J.; Colley, A.; Mark, P.; Collins, F.; et al.
2019TRAIL signals through the ubiquitin ligase MID1 to promote pulmonary fibrosisCollison, A.M.; Li, J.; De Siqueira, A.P.; Lv, X.; Toop, H.D.; Morris, J.C.; Starkey, M.R.; Hansbro, P.M.; Zhang, J.; Mattes, J.
2014SOX3 deletion in mouse and human Is associated with persistence of the craniopharyngeal canalAlatzoglou, K.; Azriyanti, A.; Rogers, N.; Ryan, F.; Curry, N.; Noakes, C.; Bignell, P.; Hall, G.; Littooij, A.; Saunders, D.; Thomas, P.; Stewart, H.; Dattani, M.
2012Sphingosine-1-phosphate facilitates trafficking of hematopoietic stem cells and their mobilization by CXCR4 antagonists in miceJuarez, J.; Harun, N.; Thien, M.; Welschinger, R.; Baraz, R.; Dela Pena, A.; Pitson, S.; Rettig, M.; DiPersio, J.; Bradstock, K.; Bendall, L.
2010Genetic dissection of differential signaling threshold requirements for the Wnt/β-Catenin pathway in vivoBuchert, M.; Athineos, D.; Abud, H.; Burke, Z.; Faux, M.; Samuel, M.; Jarnicki, A.; Winbanks, C.; Newton, I.; Meniel, V.; Suzuki, H.; Stacker, S.; Nathke, I.; Tosh, D.; Huelsken, J.; Clarke, A.; Heath, J.; Sansom, O.; Ernst, M.; Nusse, R.
2011DNMT3L is a regulator of X chromosome compaction and post-meiotic gene transcriptionZamudio, N.; Scott, H.; Wolski, K.; Lo, C.; Law, C.; Leong, D.; Kinkel, S.; Chong, S.; Jolley, D.; Smyth, G.; De Kretser, D.; Whitelaw, E.; O'Bryan, M.; Pera, M.
2018A Upf3b-mutant mouse model with behavioral and neurogenesis defectsHuang, 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.

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