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Results 1-10 of 24 (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.
1999
Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient
Gecz, J.
;
Baker, E.
;
Donnelly, A.
;
Ming, J.
;
McDonald-McGinn, D.
;
Spinner, N.
;
Zackai, E.
;
Sutherland, G.
;
Mulley, J.
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.
1995
Gene duplication of the human peptide YY gene (PYY) generated the pancreatic polypeptide gene (PPY) on chromosome 17q21.1
Hort, Y.
;
Baker, E.
;
Sutherland, G.
;
Shine, J.
;
Herzog, H.
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.
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.
Discover
Author
19
Sutherland, G.
6
Eyre, H.
5
Richards, R.
4
Hobson, L.
4
Mangelsdorf, M.
3
Callen, D.
3
Finnis, M.
2
Akkari, P.
2
Crawford, J.
2
Dayan, S.
.
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Subject
17
Base Sequence
16
Chromosome Mapping
13
In Situ Hybridization, Fluorescence
12
Amino Acid Sequence
11
Animals
10
Cloning, Molecular
10
Male
7
DNA, Complementary
7
Sequence Homology, Amino Acid
6
Chromosome Fragile Sites
.
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2000
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1999
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1998
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1997
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1996
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1995