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Results 1-10 of 15 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2004
Effect of β₂‐glycoprotein I null mutation on reproductive outcome and antiphospholipid antibody‐mediated pregnancy pathology in mice
Robertson, S.
;
Roberts, C.
;
van Beijering, E.
;
Pensa, K.
;
Sheng, Y.
;
Shi, T.
;
Krilis, S.
2006
Essential role for IL-10 in resistance to lipopolysaccharide-induced preterm labor in mice
Robertson, S.
;
Skinner, R.
;
Care, A.
2004
Inhibition of generation of cytotoxic T lymphocyte activity by a CCL19/macrophage inflammatory protein (MIP)-3beta antagonist
Pilkington, K.
;
Clark-Lewis, I.
;
McColl, S.
2001
The protein tyrosine phosphatase TCPTP suppresses the tumorigenicity of glioblastoma cells expressing a mutant epidermal growth factor receptor
Klingler-Hoffmann, M.
;
Fodero-Tavoletti, M.
;
Mishima, K.
;
Narita, Y.
;
Cavenee, W.
;
Furnari, F.
;
Huang, H.
;
Tiganis, T.
2004
Reproductive performance in female ClockΔ19 mutant mice
Kennaway, D.
;
Boden, M.
;
Voultsios, A.
2001
Impaired thrombin generation in b2-glycoprotein I null mice
Sheng, Y.
;
Reddel, S.
;
Herzog, H.
;
Wang, Y.
;
Brighton, T.
;
France, M.
;
Robertson, S.
;
Krilis, 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.
2009
Csf2 Null Mutation Alters Placental Gene Expression and Trophoblast Glycogen Cell and Giant Cell Abundance in Mice
Sferruzzi-Perri, A.
;
Macpherson, A.
;
Roberts, C.
;
Robertson, S.
2002
Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome
Lower, K.
;
Turner, G.
;
Kerr, B.
;
Mathews, K.
;
Shaw, M.
;
Gedeon, A.
;
Schelley, S.
;
Hoyme, H.
;
White, S.
;
Delatycki, M.
;
Lampe, A.
;
Clayton-Smith, J.
;
Stewart, H.
;
van Ravenswaay, C.
;
de Vries, B.
;
Cox, B.
;
Grompe, M.
;
Ross, S.
;
Thomas, P.
;
Mulley, J.
;
et al.
2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
Stromme, P.
;
Mangelsdorf, M.
;
Shaw, M.
;
Lower, K.
;
Lewis, S.
;
Bruyere, H.
;
Lutcherath, V.
;
Gedeon, A.
;
Wallace, R.
;
Scheffer, I.
;
Turner, G.
;
Partington, M.
;
Frints, S.
;
Fryns, J.
;
Sutherland, G.
;
Mulley, J.
;
Gecz, J.
Discover
Author
6
Robertson, S.
3
Shaw, M.
3
Thomas, P.
2
et al.
2
Gecz, J.
2
Gedeon, A.
2
Krilis, S.
2
Lower, K.
2
Mulley, J.
2
Roberts, C.
.
next >
Subject
8
Humans
8
Male
5
Pregnancy
4
Amino Acid Sequence
4
Molecular Sequence Data
3
Intellectual Disability
3
Mice, Inbred BALB C
3
Mice, Inbred C57BL
3
Mice, Knockout
3
Mice, Mutant Strains
.
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Date issued
2
2009
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2006
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2004
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2003
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2002
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2001