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Issue Date
Title
Author(s)
2004
HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressor
Lalonde, J.
;
Lim, R.
;
Ingley, E.
;
Tilbrook, P.
;
Thompson, M.
;
McCulloch, R.
;
Beaumont, J.
;
Wicking, C.
;
Eyre, H.
;
Sutherland, G.
;
Howe, K.
;
Solomon, E.
;
Williams, J.
;
Klinken, S.
1996
Further characterization of proteins associated with elastic fiber microfibrils including the molecular cloning of MAGP-2 (MP25)
Gibson, M.
;
Hatzinikolas, G.
;
Kumaratilake, J.
;
Sandberg, L.
;
Nicholl, J.
;
Sutherland, G.
;
Cleary, E.
1998
Molecular characterization, pharmacological properties and chromosomal localization of the human GALR2 galanin receptor
Fathi, Z.
;
Battaglino, P.
;
Iben, L.
;
Li, H.
;
Baker, E.
;
Zhang, D.
;
McGovern, R.
;
Mahle, C.
;
Sutherland, G.
;
Iismaa, T.
;
Dickinson, K.
;
Antal Zimanyi, I.
1996
DNAM-1, a novel adhesion molecule involved in the cytolytic function of T lymphocytes
Shibuya, A.
;
Campbell, D.
;
Hannum, C.
;
Yssel, H.
;
Franz-Bacon, K.
;
McClanahan, T.
;
Kitamura, T.
;
Nicholl, J.
;
Sutherland, G.
;
Lanier, L.
;
Phillips, J.
1997
The gene for the human interleukin-11 receptor alpha chain locus is highly homologous to the murine gene and contains alternatively spliced first exons
Nandurkar, H.
;
Robb, L.
;
Nicholl, J.
;
Hilton, D.
;
Sutherland, G.
;
Begley, C.
1998
Complex organisation of the 5'-end of the human glycine tRNA synthetase gene
Mudge, S.
;
Williams, J.
;
Eyre, H.
;
Sutherland, G.
;
Cowan, P.
;
Power, D.
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.
1997
AMP-activated protein kinase isoenzyme family: subunit structure and chromosomal location
Stapleton, D.
;
Woollatt, E.
;
Mitchelhill, K.
;
Nicholl, J.
;
Fernandez, C.
;
Michell, B.
;
Witters, L.
;
Power, D.
;
Sutherland, G.
;
Kemp, B.
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.
1995
A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
Steinlein, O.
;
Mulley, J.
;
Propping, P.
;
Wallace, R.
;
Phillips, H.
;
Sutherland, G.
;
Scheffer, I.
;
Berkovic, S.
Discover
Author
12
Eyre, H.
11
Baker, E.
7
Nicholl, J.
6
Copeland, N.
6
Jenkins, N.
6
Woollatt, E.
5
Gilbert, D.
5
Herzog, H.
4
Crawford, J.
4
Mulley, J.
.
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Subject
34
Molecular Sequence Data
30
Chromosome Mapping
26
Base Sequence
26
Mice
25
Amino Acid Sequence
20
Male
18
In Situ Hybridization, Fluorescence
16
DNA, Complementary
12
Cloning, Molecular
12
Female
.
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