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Results 1-10 of 10 (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.
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.
2001
MUC13, a novel human cell surface mucin expressed by epithelial and hemopoietic cells
Williams, S.
;
Wreschner, D.
;
Tran, M.
;
Eyre, H.
;
Sutherland, G.
;
McGuckin, M.
2001
Cloning and characterization of the human activity-dependent neuroprotective protein
Zamostiano, R.
;
Pinhasov, A.
;
Gelber, E.
;
Steingart, R.
;
Seroussi, E.
;
Giladi, E.
;
Bassan, M.
;
Wollman, Y.
;
Eyre, H.
;
Mulley, J.
;
Brenneman, D.
;
Gozes, I.
2001
Identification of a novel human tankyrase through its interaction with the adaptor protein Grb14
Lyons, R.
;
Deane, R.
;
Lynch, D.
;
Ye, Z.
;
Sanderson, G.
;
Eyre, H.
;
Sutherland, G.
;
Daly, R.
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.
1997
Human chromosomal fragile site FRA16B is an amplified AT-rich minisatellite repeat
Yu, S.
;
Mangelsdorf, M.
;
Hewett, D.
;
Hobson, L.
;
Baker, E.
;
Eyre, H.
;
Lapsys, N.
;
Le Paslier, D.
;
Doggett, N.
;
Sutherland, G.
;
Richards, R.
1998
FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis
Hewett, D.
;
Handt, O.
;
Hobson, L.
;
Mangelsdorf, M.
;
Eyre, H.
;
Baker, E.
;
Sutherland, G.
;
Schuffenhauer, S.
;
Mao, J.I.
;
Richards, R.
1995
Molecular cloning of the cDNA encoding human skeletal muscle triadin and its localisation to chromosome 6q22-6q23
Taske, N.
;
Eyre, H.
;
O'Brien, R.
;
Sutherland, G.
;
Denborough, M.
;
Foster, P.
1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.
Kortschak, R.
;
Reimann, H.
;
Zimmer, M.
;
Eyre, H.
;
Saint, R.
;
Jenne, D.
Discover
Author
8
Sutherland, G.
2
Baker, E.
2
Hewett, D.
2
Hobson, L.
2
Mangelsdorf, M.
2
Richards, R.
1
Anderson, G.
1
Antalis, T.
1
Barker, M.
1
Bassan, M.
.
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Subject
10
Humans
8
Base Sequence
7
Amino Acid Sequence
6
Chromosome Mapping
5
RNA, Messenger
4
DNA, Complementary
4
In Situ Hybridization, Fluorescence
4
Polymerase Chain Reaction
4
Sequence Alignment
4
Sequence Homology, Amino Acid
.
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Date issued
4
2001
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1999
2
1998
1
1997
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1995