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Results 1-10 of 45 (Search time: 0.003 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.
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.
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.
1996
Two novel frameshift mutations causing premature stop codons in a patient with the severe form of Maroteaux-Lamy syndrome
Isbrandt, D.
;
Hopwood, J.
;
von Figura, K.
;
Peters, C.
1997
A Novel Epithelial-Expressed ETS Gene, ELF3 - Human and Murine cDNA Sequences, Murine Genomic Organization, Human Mapping to 1q32.2 and Expression in Tissues and Cancer
Tymms, M.
;
Ng, A.
;
Thomas, R.
;
Schutte, B.
;
Zhou, J.
;
Eyre, H.
;
Sutherland, G.
;
Seth, A.
;
Rosenberg, M.
;
Papas, T.
;
Debouck, C.
;
Kola, I.
2015
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Muona, M.
;
Berkovic, S.
;
Dibbens, L.
;
Oliver, K.
;
Maljevic, S.
;
Bayly, M.
;
Joensuu, T.
;
Canafoglia, L.
;
Franceschetti, S.
;
Michelucci, R.
;
Markkinen, S.
;
Heron, S.
;
Hildebrand, M.
;
Andermann, E.
;
Andermann, F.
;
Gambardella, A.
;
Tinuper, P.
;
Licchetta, L.
;
Scheffer, I.
;
Criscuolo, C.
;
et al.
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.
2006
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation
Hagens, O.
;
Dubos, A.
;
Abidi, F.
;
Barbi, G.
;
Van Zutven, L.
;
Hoeltzenbein, M.
;
Tommerup, N.
;
Moraine, C.
;
Fryns, J.
;
Chelly, J.
;
van Bokhoven, H.
;
Gecz, J.
;
Dollfus, H.
;
Ropers, H.
;
Schwartz, C.
;
de Cassia Stocco dos Santos, R.
;
Kalscheuer, V.
;
Hanauer, A.
2000
Gene encoding the mouse sulphamidase: cDNA cloning, structure, and chromosomal mapping
Costanzi, E.
;
Beccari, T.
;
Stinchi, S.
;
Bibi, L.
;
Hopwood, J.
;
Orlacchio, A.
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.
Discover
Author
25
Sutherland, G.
10
Eyre, H.
7
Baker, E.
7
Hopwood, J.
6
Gecz, J.
5
Crawford, J.
4
et al.
4
Haan, E.
4
Nicholl, J.
3
Berkovic, S.
.
next >
Subject
40
Humans
24
Animals
23
Cloning, Molecular
21
Sequence Homology, Amino Acid
20
Chromosome Mapping
19
DNA, Complementary
13
Male
13
Mice
13
Sequence Alignment
12
Female
.
next >
Date issued
3
2010 - 2015
13
2000 - 2009
29
1994 - 1999