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Results 1-10 of 14 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
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.
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.
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.
2010
The first intestinal motility patterns in fetal mice are not mediated by neurons or interstitial cells of Cajal
Roberts, R.
;
Ellis, M.
;
Gwynne, R.
;
Bergner, A.
;
Lewis, M.
;
Spencer, E.
;
Bornstein, J.
;
Young, H.
2012
Sphingosine-1-phosphate facilitates trafficking of hematopoietic stem cells and their mobilization by CXCR4 antagonists in mice
Juarez, J.
;
Harun, N.
;
Thien, M.
;
Welschinger, R.
;
Baraz, R.
;
Dela Pena, A.
;
Pitson, S.
;
Rettig, M.
;
DiPersio, J.
;
Bradstock, K.
;
Bendall, L.
2012
Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic mice
Lee, K.
;
Tan, J.
;
Morris, M.
;
Rizzoti, K.
;
Hughes, J.
;
Cheah, P.
;
Felquer, F.
;
Liu, X.
;
Piltz, S.
;
Lovell-Badge, R.
;
Thomas, P.
;
Schmidt, J.V.
Discover
Author
3
Hughes, J.
3
Paton, J.
2
Corbett, M.
2
Dibbens, L.
2
et al.
2
Gardner, A.
2
Kivity, S.
2
Scott, H.
2
Thomas, P.
1
Abud, H.
.
next >
Subject
14
Animals
7
Humans
4
Cells, Cultured
4
Mice, Inbred C57BL
4
Mice, Knockout
4
Mutation
3
Adult
3
Middle Aged
3
Neurons
2
Aged
.
next >
Date issued
2
2017
2
2015
2
2013
3
2012
2
2011
3
2010