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Results 1-10 of 19 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2016CXCR5⁺ follicular cytotoxic T cells control viral infection in B cell folliclesLeong, Y.; Chen, Y.; Ong, H.; Wu, D.; Man, K.; Deleage, C.; Minnich, M.; Meckiff, B.; Wei, Y.; Hou, Z.; Zotos, D.; Fenix, K.; Atnerkar, A.; Preston, S.; Chipman, J.; Beilman, G.; Allison, C.; Sun, L.; Wang, P.; Xu, J.; et al.
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.
2017IL-17-producing γδ T cells switch migratory patterns between resting and activated statesMcKenzie, D.; Kara, E.; Bastow, C.; Tyllis, T.; Fenix, K.; Gregor, C.; Wilson, J.; Babb, R.; Paton, J.; Kallies, A.; Nutt, S.; Brüstle, A.; Mack, M.; Comerford, I.; McColl, S.
2018The Factor Inhibiting HIF asparaginyl hydroxylase regulates oxidative metabolism and accelerates metabolic adaptation to hypoxiaSim, J.; Cowburn, A.S.; Palazon, A.; Madhu, B.; Tyrakis, P.A.; Macias, D.; Bargiela, D.M.; Pietsch, S.; Gralla, M.; Evans, C.E.; Kittipassorn, T.; Chey, Y.C.J.; Branco, C.M.; Rundqvist, H.; Peet, D.J.; Johnson, R.S.
2015Characterization of pneumococcal genes involved in bloodstream invasion in a mouse modelMahdi, L.; Van der Hoek, M.; Ebrahimie, E.; Paton, J.; Ogunniyi, A.; Metzger, D.W.
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.
2015Identification of markers that functionally define a quiescent multiple myeloma cell sub-population surviving bortezomib treatmentAdomako, A.; Calvo, V.; Biran, N.; Osman, K.; Chari, A.; Paton, J.; Paton, A.; Moore, K.; Schewe, D.; Aguirre-Ghiso, J.
2010A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24Bahlo, M.; Jolly, L.; Afawi, Z.; Gardner, A.; Oliver, K.; Tan, S.; Coffey, A.; Mulley, J.; Dibbens, L.; Simri, W.; Shalata, A.; Kivity, S.; Jackson, G.; Berkovic, S.; Gecz, J.; Corbett, M.
2011Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearingFasquelle, 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.
2013Mutations in DEPDC5 cause familial focal epilepsy with variable fociDibbens, L.; de Vries, B.; Donatello, S.; Heron, S.; Hodgson, B.; Chintawar, S.; Crompton, D.; Hughes, J.; Bellows, S.; Klein, K.; Callenbach, P.; Corbett, M.; Gardner, A.; Kivity, S.; Iona, X.; Regan, B.; Weller, C.; Crimmins, D.; O'Brien, T.; Guerrero-Lopez, R.; et al.

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