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Results 1-10 of 19 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2016
CXCR5⁺ follicular cytotoxic T cells control viral infection in B cell follicles
Leong, 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.
2017
NAD deficiency, congenital malformations, and niacin supplementation
Shi, 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.
2017
IL-17-producing γδ T cells switch migratory patterns between resting and activated states
McKenzie, 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.
2018
The Factor Inhibiting HIF asparaginyl hydroxylase regulates oxidative metabolism and accelerates metabolic adaptation to hypoxia
Sim, 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.
2015
Characterization of pneumococcal genes involved in bloodstream invasion in a mouse model
Mahdi, L.
;
Van der Hoek, M.
;
Ebrahimie, E.
;
Paton, J.
;
Ogunniyi, A.
;
Metzger, D.W.
2014
SOX3 deletion in mouse and human Is associated with persistence of the craniopharyngeal canal
Alatzoglou, 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.
2015
Identification of markers that functionally define a quiescent multiple myeloma cell sub-population surviving bortezomib treatment
Adomako, A.
;
Calvo, V.
;
Biran, N.
;
Osman, K.
;
Chari, A.
;
Paton, J.
;
Paton, A.
;
Moore, K.
;
Schewe, D.
;
Aguirre-Ghiso, J.
2010
A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24
Bahlo, 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.
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
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, 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.
Discover
Author
4
Paton, J.
3
et al.
3
Hughes, J.
3
Thomas, P.
2
Corbett, M.
2
Dibbens, L.
2
Fenix, K.
2
Gardner, A.
2
Kivity, S.
2
McColl, S.
.
next >
Subject
19
Animals
14
Female
10
Humans
6
Mice, Inbred C57BL
5
Cells, Cultured
5
Mice, Knockout
4
Mice, Inbred BALB C
4
Mutation
3
Adult
3
Blotting, Western
.
next >
Date issued
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2018
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2017
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2015
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2014
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2013
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2012
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2011
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2010