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Results 1-10 of 18 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1995
The brn-2 gene regulates the melanocytic phenotype and tumorigenic potential of human melanoma cells
Angus, J.
;
Thompson, F.
;
Murphy, K.
;
Baker, E.
;
Sutherland, G.
;
Parsons, P.
;
Sturm, R.
1995
Assignment of the human skeletal muscle a-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization
Eyre, H.
;
Akkari, P.
;
Wilton, S.
;
Callen, D.
;
Baker, E.
;
Laing, N.
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.
1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation
Hunt, C.
;
Eyre, H.
;
Akkari, P.
;
Meredith, C.
;
Dorosz, S.
;
Wilton, S.
;
Callen, D.
;
Laing, N.
;
Baker, E.
1995
Localisation of the adenosine A2b receptor subtype (ADORA2B) to chromosome 17p11.2-p12 by FISH and PCR screening of somatic cell hybrids
Townsend-Nicholson, A.
;
Baker, E.
;
Sutherland, G.
;
Schofield, P.
1999
Myeloid DAP12-associating lectin (MDL)-1 is a cell surface receptor involved in the activation of myeloid cells
Baker, E.
;
Sutherland, G.
;
Phillips, J.
;
Lanier, L.
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.
2005
Common chromosomal fragile site FRA16D mutation in cancer cells
Finnis, M.
;
Dayan, S.
;
Hobson, L.
;
Chenevix-Trench, G.
;
Friend, K.
;
Ried, K.
;
Venter, D.
;
Woollatt, E.
;
Baker, E.
;
Richards, R.
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.
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.
Discover
Author
2
Schofield, P.
2
Townsend-Nicholson, A.
2
Wilton, S.
2
Yu, S.
1
Adams, J.
1
Angus, J.
1
Antal Zimanyi, I.
1
Antalis, T.
1
Battaglino, P.
1
Bernand, O.
.
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Subject
17
Humans
12
Chromosome Mapping
10
Animals
9
Cloning, Molecular
9
In Situ Hybridization, Fluorescence
8
Amino Acid Sequence
7
Male
6
DNA, Complementary
6
Mice
5
Polymerase Chain Reaction
.
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Date issued
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2005
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1999
2
1998
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1997
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1996
8
1995