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Results 31-40 of 45 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
2013
Interplay between manganese and iron in pneumococcal pathogenesis: Role of the orphan response regulator ritR
Ong, C.
;
Potter, A.
;
Trappetti, C.
;
Walker, M.
;
Jennings, M.
;
Paton, J.
;
McEwan, A.
;
Payne, S.M.
2007
Contributions of pneumolysin, pneumococcal surface protein A (PspA), and PspC to pathogenicity of Streptococcus pneumoniae D39 in a mouse model
Ogunniyi, A.
;
Le Messurier, K.
;
Graham, R.
;
Watt, J.
;
Briles, D.
;
Stroeher, U.
;
Paton, J.
2014
Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth
Homan, C.
;
Kumar, R.
;
Nguyen, L.
;
Haan, E.
;
Raymond, F.
;
Abidi, F.
;
Raynaud, M.
;
Schwartz, C.
;
Wood, S.
;
Gecz, J.
;
Jolly, L.
2012
Identification of a novel pneumococcal vaccine antigen preferentially expressed during meningitis in mice
Mahdi, L.
;
Wang, H.
;
Van der Hoek, M.
;
Paton, J.
;
Ogunniyi, A.
2006
Null mutation in transforming growth factor β1 disrupts ovarian function and causes oocyte incompetence and early embryo arrest
Ingman, W.
;
Robker, R.
;
Woittiez, K.
;
Robertson, S.
2008
Resistance to mucosal lysozyme compensates for the fitness deficit of peptidoglycan modifications by Streptococcus pneumoniae
Davis, K.
;
Akinbi, H.
;
Standish, A.
;
Weiser, J.
;
Gilmore, M.S.
2007
Transforming growth factor-β1 null mutation causes infertility in male mice associated with testosterone deficiency and sexual dysfunction
Ingram, W.
;
Robertson, S.
2010
Canal cristae growth and fiber extension to the outer hair cells of the mouse ear require Prox1 activity
Fritzsch, B.
;
Dillard, M.
;
Lavado, A.
;
Harvey, N.
;
Israt, J.
;
Koch, K.-W.
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.
1998
PAK3 mutation in nonsyndromic X-linked mental retardation
Allen, K.
;
Gleeson, J.
;
Bagrodia, S.
;
Partington, M.
;
MacMillan, J.
;
Cerione, R.
;
Mulley, J.
;
Walsh, C.
Discover
Author
11
Gecz, J.
9
et al.
6
Robertson, S.
5
Jolly, L.
5
Paton, J.
5
Shaw, M.
4
Gardner, A.
4
Mulley, J.
4
Ogunniyi, A.
4
Shoubridge, C.
.
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Subject
31
Male
30
Humans
14
Intellectual Disability
12
Pedigree
11
Molecular Sequence Data
10
Amino Acid Sequence
9
Mice, Knockout
6
Bacterial Proteins
6
Brain
6
Mice, Inbred C57BL
.
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Date issued
28
2010 - 2019
15
2000 - 2009
1
1990 - 1999
1
1987 - 1989