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News / The University of Adelaide Libraries [1993-2001]
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Results 1-10 of 25 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
1996
The stoned locus of drosophila melanogaster produces a dicistronic transcript and encodes two distinct polypeptides
Andrews, J.
;
Smith, M.
;
Merakovsky, J.
;
Coulson, M.
;
Hannan, F.
;
Kelly, L.
2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitus
Raymond, F.
;
Tarpey, P.
;
Edkins, S.
;
Tofts, C.
;
O'Meara, S.
;
Teague, J.
;
Butler, A.
;
Stevens, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Dicks, E.
;
Gray, K.
;
Harrison, R.
;
Hills, K.
;
Hinton, J.
;
Jones, D.
;
Menzies, A.
;
Perry, J.
;
Raine, K.
;
et al.
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.
1996
bcl-w, a novel member of the bcl-2 family, promotes cell survival
Gibson, L.
;
Holmgreen, S.
;
Huang, D.
;
Bernand, O.
;
Copeland, N.
;
Jenkins, N.
;
Sutherland, G.
;
Baker, E.
;
Adams, J.
;
Cory, S.
2007
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation
Tarpey, P.
;
Raymond, F.
;
Nguyen, L.
;
Rodriguez, J.
;
Hackett, A.
;
Vandeleur, L.
;
Smith, R.
;
Shoubridge, C.
;
Edkins, S.
;
Stevens, C.
;
O'Meara, S.
;
Tofts, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Halliday, K.
;
Hills, K.
;
Jones, D.
;
Mironenko, T.
;
Perry, J.
;
et al.
1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
Gedeon, A.
;
Colley, A.
;
Jamieson, R.
;
Thompson, E.
;
Rogers, J.
;
Sillence, D.
;
Tiller, G.
;
Mulley, J.
;
Gecz, J.
2015
Rice SPX-Major Facility Superfamily3, a vacuolar phosphate efflux transporter, is involved in maintaining phosphate homeostasis in rice
Wang, C.
;
Yue, W.
;
Ying, Y.
;
Wang, S.
;
Secco, D.
;
Liu, Y.
;
Whelan, J.
;
Tyerman, S.
;
Shou, H.
1999
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM
Friend, K.
;
Crimmins, D.
;
Phan, T.
;
Sue, C.
;
Colley, A.
;
Fung, V.
;
Morris, J.
;
Sutherland, G.
;
Richards, R.
2010
Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome
Gecz, J.
2010
Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination
Pearlman, A.
;
Loke, J.
;
Le Caignec, C.
;
White, S.
;
Chin, L.
;
Friedman, A.
;
Warr, N.
;
Willan, J.
;
Brauer, D.
;
Farmer, C.
;
Brooks, E.
;
Oddoux, C.
;
Riley, B.
;
Shajahan, S.
;
Camerino, G.
;
Homfray, T.
;
Crosby, A.
;
Couper, J.
;
David, A.
;
Greenfield, A.
;
et al.
Discover
Author
6
Gecz, J.
6
Sutherland, G.
5
Mulley, J.
4
Gedeon, A.
4
Scheffer, I.
3
Baker, E.
3
Berkovic, S.
3
et al.
3
Tarpey, P.
3
Wallace, R.
.
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Subject
24
Molecular Sequence Data
21
Humans
20
Male
14
Animals
13
Base Sequence
13
Pedigree
8
Mutation
5
Family Health
5
Proteins
5
RNA, Messenger
.
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Date issued
5
2010 - 2015
9
2000 - 2009
11
1995 - 1999