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Issue Date
Title
Author(s)
1998
Development of a two-dimensional gel electrophoresis database of human lysosomal proteins
Chataway, T.
;
Whittle, A.
;
Lewis, M.
;
Bindloss, C.
;
Moritz, R.
;
Simpson, R.
;
Hopwood, J.
;
Meikle, P.
2010
Dissemination and genetic context analysis of bla(VIM-6) among Pseudomonas aeruginosa isolates in Asian-Pacific Nations
Castanheira, M.
;
Bell, J.
;
Turnidge, J.
;
Mendes, R.
;
Jones, R.
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
Fragile XE-associated familial mental retardation protein 2 (FMR2) acts as a potent transcription activator
Hillman, M.
;
Gecz, J.
2011
Gaucher disease in sheep
Karageorgos, L.
;
Lancaster, M.
;
Nimmo, J.
;
Hopwood, J.
2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Heron, S.
;
Grinton, B.
;
Kivity, S.
;
Afawi, Z.
;
Zuberi, S.
;
Hughes, J.
;
Pridmore, C.
;
Hodgson, B.
;
Iona, X.
;
Sadleir, L.
;
Pelekanos, J.
;
Herlenius, E.
;
Goldberg-Stern, H.
;
Bassan, H.
;
Haan, E.
;
Korczyn, A.
;
Gardner, A.
;
Corbett, M.
;
Gecz, J.
;
Thomas, P.
;
et al.
2008
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation
Froyen, G.
;
Corbett, M.
;
Vandewalle, J.
;
Jarvela, I.
;
Lawrence, O.
;
Meldrum, C.
;
Bauters, M.
;
Govaerts, K.
;
Vandeleur, L.
;
Van Esch, H.
;
Chelly, J.
;
Sanlaville, D.
;
van Bokhoven, H.
;
Ropers, H.
;
Laumonnier, F.
;
Ranieri, E.
;
Schwartz, C.
;
Abidi, F.
;
Tarpey, P.
;
Futreal, P.
;
et al.
2010
Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly
Giannandrea, M.
;
Bianchi, V.
;
Mignogna, M.
;
Sirri, A.
;
Carrabino, S.
;
D'Elia, E.
;
Vecellio, M.
;
Russo, S.
;
Cogliati, F.
;
Larizza, L.
;
Ropers, H.
;
Tzschach, A.
;
Kalscheuer, V.
;
Oehl-Jaschkowitz, B.
;
Skinner, C.
;
Schwartz, C.
;
Gecz, J.
;
Van Esch, H.
;
Raynaud, M.
;
Chelly, J.
;
et al.
2010
Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome
Gecz, J.
Discover
Author
58
Sutherland, G.
26
Gecz, J.
24
Eyre, H.
22
Hopwood, J.
21
Baker, E.
15
et al.
12
Haan, E.
10
Woollatt, E.
9
Callen, D.
9
Ropers, H.
.
next >
Subject
82
Base Sequence
79
Amino Acid Sequence
59
Animals
53
Male
48
Chromosome Mapping
41
Female
33
Cloning, Molecular
33
Sequence Homology, Amino Acid
32
Mice
29
DNA, Complementary
.
next >
Date issued
11
2010 - 2014
53
2000 - 2009
74
1994 - 1999