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Results 41-50 of 79 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2004
HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressor
Lalonde, J.
;
Lim, R.
;
Ingley, E.
;
Tilbrook, P.
;
Thompson, M.
;
McCulloch, R.
;
Beaumont, J.
;
Wicking, C.
;
Eyre, H.
;
Sutherland, G.
;
Howe, K.
;
Solomon, E.
;
Williams, J.
;
Klinken, S.
2005
Mutation of the androgen receptor causes oncogenic transformation of the prostate
Han, G.
;
Buchanan, G.
;
Ittmann, M.
;
Harris, J.
;
Yu, X.
;
DeMayo, F.
;
Tilley, W.
;
Greenberg, N.
2004
Regulation of neuronal voltage-gated sodium channels by the ubiquitin-protein ligases Nedd4 and Nedd4-2
Fotia, A.
;
Ekberg, J.
;
Adams, D.
;
Cook, D.
;
Poronnik, P.
;
Kumar, S.
2004
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation
Weaving, L.
;
Christodoulou, J.
;
Williamson, S.
;
Friend, K.
;
McKenzie, O.
;
Archer, H.
;
Evans, J.
;
Clarke, A.
;
Pelka, G.
;
Tam, P.
;
Watson, C.
;
Lahooti, H.
;
Ellaway, C.
;
Bennetts, B.
;
Leonard, H.
;
Gecz, J.
2004
Refinement of a therapeutic Shiga toxin-binding probiotic for human trials
Pinyon, R.
;
Paton, J.
;
Paton, A.
;
Botten, J.
;
Morona, R.
2007
A pneumococcal MerR-like regulator and S-nitrosoglutathione reductase are required for systemic virulence
Stroeher, U.
;
Kidd, S.
;
Stafford, S.
;
Jennings, M.
;
Paton, J.
;
McEwan, A.
2007
Evolutionary and expression analysis of the zebrafish deubiquitylating enzyme, Usp9
Khut, P.
;
Tucker, B.
;
Lardelli, M.
;
Wood, S.
2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation
Burdon, K.
;
McKay, J.
;
Sale, M.
;
Russell-Eggitt, I.
;
Mackey, D.
;
Wirth, G.
;
Elder, J.
;
Nicoll, A.
;
Clarke, M.
;
FitzGerald, L.
;
Stankovich, J.
;
Shaw, M.
;
Sharma, S.
;
Gajovic, S.
;
Gruss, P.
;
Ross, S.
;
Thomas, P.
;
Voss, A.
;
Thomas, T.
;
Gecz, J.
;
et al.
2001
A novel missense mutation in lysosomal sulfamidase is the basis of MPS III A in a spontaneous mouse mutant
Bhattacharyya, R.
;
Gliddon, B.
;
Beccari, T.
;
Hopwood, J.
;
Stanley, P.
2004
Immunoneutralization of growth differentiation factor 9 reveals it partially accounts for mouse oocyte mitogenic activity
Gilchrist, R.
;
Ritter, L.
;
Cranfield, M.
;
Jeffrey, L.
;
Amato, F.
;
Scott, S.
;
Myllymaa, S.
;
Kaivo-Oja, N.
;
Lankinen, H.
;
Mottershead, D.
;
Groome, N.
;
Ritvos, O.
Discover
Author
8
Sutherland, G.
6
Paton, J.
5
Eyre, H.
5
Gecz, J.
5
Hopwood, J.
5
Kumar, S.
4
Forbes, B.
4
Whitelaw, M.
3
Beccari, T.
3
Booker, G.
.
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Subject
79
Animals
56
Amino Acid Sequence
54
Humans
28
Base Sequence
24
Sequence Homology, Amino Acid
19
Female
16
Mutation
14
Protein Structure, Tertiary
13
Male
13
Protein Binding
.
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Date issued
5
2009
9
2008
6
2007
5
2006
5
2005
15
2004
6
2003
11
2002
10
2001
7
2000
.
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