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Results 1-10 of 10 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
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.
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.
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.
2006
Production and characterization of monoclonal antibodies against insulin-like growth factor type 1 receptor
Keyhanfar, M.
;
Forbes, B.
;
Cosgrove, L.
;
Wallace, J.
;
Booker, G.
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.
2008
Platypus Pou5f1 reveals the first steps in the evolution of trophectoderm differentiation and pluripotency in mammals
Niwa, H.
;
Sekita, Y.
;
Tsend-Ayush, E.
;
Grutzner, F.
2004
LGI1 mutations in temporal lobe epilepsies
Berkovic, S.
;
Izzillo, P.
;
McMahon, J.
;
Harkin, L.
;
McIntosh, A.
;
Phillips, H.
;
Briellmann, R.
;
Wallace, R.
;
Mazarib, A.
;
Neufeld, M.
;
Korczyn, A.
;
Scheffer, I.
;
Mulley, J.
2001
TTYH2, a human homologue of the Drosophila melanogaster gene tweety, is located on 17q24 and upregulated in renal cell carcinoma
Rae, F.
;
Hooper, J.
;
Eyre, H.
;
Sutherland, G.
;
Nicol, D.
;
Clements, J.
2002
Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c
Schwarz, Q.
;
Cox, T.
Discover
Author
3
Mulley, J.
3
Shaw, M.
2
et al.
2
Gecz, J.
2
Gedeon, A.
2
Lower, K.
2
Ross, S.
2
Scheffer, I.
2
Sutherland, G.
2
Thomas, P.
.
next >
Subject
10
Animals
9
Amino Acid Sequence
6
Male
5
Sequence Alignment
4
Mutation
4
Pedigree
3
Intellectual Disability
3
Mutation, Missense
3
X Chromosome
2
Base Sequence
.
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2001