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Results 1-10 of 12 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1999
Testisin, a new human serine proteinase expressed by premeiotic testicular germ cells and lost in testicular germ cell tumors
Hooper, J.
;
Nicol, D.
;
Dickinson, J.
;
Eyre, H.
;
Scarman, A.
;
Normyle, J.
;
Stuttgen, M.
;
Douglas, M.
;
Loveland, K.
;
Sutherland, G.
;
Antalis, T.
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.
2001
HPP1: A transmembrane protein-encoding gene commonly methylated in colorectal polyps and cancers
Young, J.
;
Biden, K.
;
Simms, L.
;
Huggard, P.
;
Karamatic, R.
;
Eyre, H.
;
Sutherland, G.
;
Herath, N.
;
Barker, M.
;
Anderson, G.
;
Fitzpatrick, D.
;
Ramm, G.
;
Jass, J.
;
Leggett, B.
1999
Characterization and chromosomal localization of USP3, a novel human ubiquitin-specific protease
Sloper-Mould, K.
;
Eyre, H.
;
Wang, X.W.
;
Sutherland, G.
;
Baker, R.
1997
LAIR-1, a novel inhibitory receptor expressed on human mononuclear leukocytes
Meyaard, L.
;
Adema, G.
;
Chang, C.
;
Woollatt, E.
;
Sutherland, G.
;
Lanier, L.
;
Phillips, J.
1999
Molecular cloning and characterization of a cDNA encoding the human leucocyte vacuolar protein sorting (h1Vps45)
Rajasekariah, P.
;
Eyre, H.
;
Stanley, K.
;
Walls, R.
;
Sutherland, G.
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.
2000
Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells
Ried, K.
;
Finnis, M.
;
Hobson, L.
;
Mangelsdorf, M.
;
Dayan, S.
;
Nancarrow, J.
;
Woollatt, E.
;
Kremmidiotis, G.
;
Gardner, A.
;
Venter, D.
;
Baker, E.
;
Richards, R.
1995
Cloning of the sulphamidase gene and identification of mutations in Sanfilippo A syndrome
Scott, H.
;
Blanch, L.
;
Guo, X.H.
;
Freeman, C.
;
Orsborn, A.
;
Baker, E.
;
Sutherland, G.
;
Morris, C.
;
Hopwood, J.
1998
Preferential pre-mRNA utilisation of an upstream cryptic 5' splice site created by a single base deletion mutation in exon 37 of the FBN-1 gene
Gibson, M.
;
Ellis, S.
;
Ades, L.
;
Haan, E.
;
Cleary, E.
Discover
Author
8
Sutherland, G.
6
Eyre, H.
3
Baker, E.
2
Crawford, J.
2
Woollatt, E.
1
Adema, G.
1
Ades, L.
1
Anderson, G.
1
Antalis, T.
1
Baker, R.
.
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Subject
12
Humans
11
Molecular Sequence Data
10
Base Sequence
7
Cloning, Molecular
6
Male
5
Chromosome Mapping
5
Sequence Homology, Amino Acid
4
DNA, Complementary
4
Female
4
Membrane Proteins
.
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