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Issue Date
Title
Author(s)
1997
Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3
Mitchison, H.
;
Munroe, P.
;
O'Rawe, A.
;
Taschner, P.
;
De Vos, N.
;
Kremmidiotis, G.
;
Lensink, I.
;
Munk, A.
;
D'Arigo, K.
;
Anderson, J.
;
Lerner, T.
;
Moyzis, R.
;
Callen, D.
;
Breuning, M.
;
Doggett, N.
;
Gardiner, R.
;
Mole, S.
1995
Mechanisms of small ring formation suggested by the molecular characterization of 2 small accessory ring chromosomes derived from chromosome 4
Fang, Y.
;
Eyre, H.
;
Bohlander, S.
;
Estop, A.
;
McPherson, E.
;
Trager, T.
;
Riess, O.
;
Callen, D.
1996
Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow
Fairbairn, L.
;
Lashford, L.
;
Spooncer, E.
;
McDermott, R.
;
Lebens, G.
;
Arrand, J.
;
Arrand, J.
;
Bellantuono, I.
;
Holt, R.
;
Hatton, C.
;
Cooper, A.
;
Besley, G.
;
Wraith, J.
;
Anson, D.
;
Hopwood, J.
;
Dexter, T.
1996
Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients
Litjens, T.
;
Brooks, D.
;
Peters, C.
;
Gibson, G.
;
Hopwood, J.
2000
FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutations
Gecz, J.
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.
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.
2008
Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform
Sharma, S.
;
Burdon, K.
;
Dave, A.
;
Jamieson, R.
;
Yaron, Y.
;
Billson, F.
;
van Maldergem, L.
;
Lorenz, B.
;
Gecz, J.
;
Craig, J.
2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitus
Raymond, F.
;
Tarpey, P.
;
Edkins, S.
;
Tofts, C.
;
O'Meara, S.
;
Teague, J.
;
Butler, A.
;
Stevens, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Dicks, E.
;
Gray, K.
;
Harrison, R.
;
Hills, K.
;
Hinton, J.
;
Jones, D.
;
Menzies, A.
;
Perry, J.
;
Raine, K.
;
et al.
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.
Discover
Author
44
Sutherland, G.
20
Eyre, H.
18
Gecz, J.
15
Baker, E.
13
Hopwood, J.
12
Haan, E.
9
et al.
8
Callen, D.
7
Crawford, J.
6
Nicholl, J.
.
next >
Subject
82
Molecular Sequence Data
42
Amino Acid Sequence
42
Animals
38
Male
37
Chromosome Mapping
28
Female
26
Cloning, Molecular
25
DNA Primers
25
DNA, Complementary
22
Mice
.
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Date issued
9
2010 - 2014
31
2000 - 2009
56
1994 - 1999