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Results 1-10 of 14 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2000
Differences in the skin peptides of the male and female Australian tree frog Litoria splendida: The discovery of the aquatic male sex pheromone splendipherin, together with Phe8 caerulein and a new antibiotic peptide caerin 1.10
Wabnitz, P.
;
Bowie, J.
;
Tyler, M.
;
Wallace, J.
;
Smith, B.
2005
Identification and characterization of avihepadnaviruses isolated from exotic anseriformes maintained in captivity
Guo, H.
;
Mason, W.
;
Aldrich, C.
;
Saputelli, J.
;
Miller, D.
;
Jilbert, A.
;
Newbold, J.
2000
Molecular cloning and characterisation of GPR74 a novel G-protein coupled receptor closest related to the Y-receptor family
Parker, R.
;
Copeland, N.
;
Eyre, H.
;
Liu, M.
;
Gilbert, D.
;
Crawford, J.
;
Couzens, M.
;
Sutherland, G.
;
Jenkins, N.
;
Herzog, H.
2000
Cytochrome P450 4A, peroxisomal enzymes and nicotinamide cofactors in koala liver
Ngo, S.
;
Kong, S.
;
Kirlich, A.
;
McKinnon, R.
;
Stupans, I.
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.
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
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.
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
4
Mulley, J.
4
Sutherland, G.
3
Scheffer, I.
3
Shaw, M.
2
Berkovic, S.
2
et al.
2
Eyre, H.
2
Gecz, J.
2
Gedeon, A.
2
Lower, K.
.
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Subject
13
Molecular Sequence Data
11
Humans
7
Mice
6
Base Sequence
5
Pedigree
5
Sequence Alignment
4
Mutation
4
Rats
4
Species Specificity
3
Conserved Sequence
.
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