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Results 11-20 of 26 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2003
Development of a diagnostic PCR assay that targets a heat-shock protein gene (groES) for detection of Pseudomonas spp. in cystic fibrosis patients
Clarke, L.
;
Moore, J.
;
Millar, B.
;
Garske, L.
;
Xu, J.
;
Heuzenroeder, M.
;
Crowe, M.
;
Elborn, J.
2009
Identifying candidate serum biomarkers of exposure to tunicamycins in rats using two-dimensional electrophoresis
Penno, M.
;
Bacic, A.
;
Colegate, S.
;
Hoffmann, P.
;
Michalski, W.
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.
2009
Thioredoxin reductase is essential for protection of neisseria gonorrhoeae against killing by nitric oxide and for bacterial growth during interaction with cervical epithelial cells
Potter, A.
;
Kidd, S.
;
Edwards, J.
;
Falsetta, M.
;
Apicella, M.
;
Jennings, M.
;
McEwan, A.
2001
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy
Phillips, H.
;
Favre, I.
;
Kirkpatrick, M.
;
Zuberi, S.
;
Goudie, D.
;
Heron, S.
;
Scheffer, I.
;
Sutherland, G.
;
Berkovic, S.
;
Bertrand, D.
;
Mulley, J.
2001
Neuronal sodium-channel a1-subunit mutations in generalized epilepsy with febrile seizures plus
Wallace, R.
;
Scheffer, I.
;
Barnett, S.
;
Richards, M.
;
Dibbens, L.
;
Desai, R.
;
Lerman-Sagie, T.
;
Lev, D.
;
Mazarib, A.
;
Brand, N.
;
Ben-Zeev, B.
;
Goikhman, I.
;
Singh, R.
;
Kremmidiotis, G.
;
Gardner, A.
;
Sutherland, G.
;
George Jr., A.
;
Mulley, J.
;
Berkovic, S.
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.
2007
DMRT gene cluster analysis in the platypus: New insights into genomic organization and regulatory regions
El-Mogharbel, N.
;
Wakefield, M.
;
Deakin, J.
;
Tsend-Ayush, E.
;
Grutzner, F.
;
Alsop, A.
;
Ezaz, T.
;
Graves, J.
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
5
Mulley, J.
4
Scheffer, I.
3
Adelson, D.
3
Berkovic, S.
3
Clark-Lewis, I.
3
et al.
3
Grutzner, F.
3
McColl, S.
3
Sutherland, G.
3
Townley, S.
.
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Subject
21
Animals
18
Amino Acid Sequence
17
Humans
14
Male
11
Mice
7
Base Sequence
7
Mutation
6
Sequence Homology, Amino Acid
5
Evolution, Molecular
5
Pedigree
.
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Date issued
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2009
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2003
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2001