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Results 1-10 of 15 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2003
RegR, a global LacI/GalR family regulator, modulates virulence and competence in Streptococcus pneumoniae
Chapuy-Regaud, S.
;
Ogunniyi, A.
;
Diallo, N.
;
Huet, Y.
;
Desnottes, J.
;
Paton, J.
;
Escaich, S.
;
Trombe, M.
1995
Comparative toxicity and virulence of Escherichia coli clones expressing variant and chimeric Shiga-like toxin type II operons
Paton, A.
;
Bourne, A.
;
Manning, P.
;
Paton, J.
1998
Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B
Wallace, R.
;
Wang, D.
;
Singh, R.
;
Scheffer, I.
;
George Jnr., A.
;
Phillips, H.
;
Saar, K.
;
Reis, A.
;
Johnson, E.
;
Sutherland, G.
;
Berkovic, S.
;
Mulley, J.
2010
A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24
Bahlo, M.
;
Jolly, L.
;
Afawi, Z.
;
Gardner, A.
;
Oliver, K.
;
Tan, S.
;
Coffey, A.
;
Mulley, J.
;
Dibbens, L.
;
Simri, W.
;
Shalata, A.
;
Kivity, S.
;
Jackson, G.
;
Berkovic, S.
;
Gecz, J.
;
Corbett, M.
2010
Functional and structural diversification of the Anguimorpha lizard venom system
Scanlon, D.
2001
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy
Phillips, H.
;
Favre, I.
;
Kirkpatrick, M.
;
Zuberi, S.
;
Goudie, D.
;
Heron, S.
;
Scheffer, I.
;
Sutherland, G.
;
Berkovic, S.
;
Bertrand, D.
;
Mulley, J.
2007
DMRT gene cluster analysis in the platypus: New insights into genomic organization and regulatory regions
El-Mogharbel, N.
;
Wakefield, M.
;
Deakin, J.
;
Tsend-Ayush, E.
;
Grutzner, F.
;
Alsop, A.
;
Ezaz, T.
;
Graves, J.
2002
Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome
Lower, K.
;
Turner, G.
;
Kerr, B.
;
Mathews, K.
;
Shaw, M.
;
Gedeon, A.
;
Schelley, S.
;
Hoyme, H.
;
White, S.
;
Delatycki, M.
;
Lampe, A.
;
Clayton-Smith, J.
;
Stewart, H.
;
van Ravenswaay, C.
;
de Vries, B.
;
Cox, B.
;
Grompe, M.
;
Ross, S.
;
Thomas, P.
;
Mulley, J.
;
et al.
2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
Stromme, P.
;
Mangelsdorf, M.
;
Shaw, M.
;
Lower, K.
;
Lewis, S.
;
Bruyere, H.
;
Lutcherath, V.
;
Gedeon, A.
;
Wallace, R.
;
Scheffer, I.
;
Turner, G.
;
Partington, M.
;
Frints, S.
;
Fryns, J.
;
Sutherland, G.
;
Mulley, J.
;
Gecz, J.
2009
The genome sequence of Taurine cattle: a window to ruminant biology and evolution
Bovine Genome Sequencing and Analysis Consortium,
;
Elsik, C.
;
Tellam, R.
;
Worley, K.
;
Adelson, David Louis
Discover
Author
6
Mulley, J.
3
Berkovic, S.
3
Scheffer, I.
3
Sutherland, G.
2
Gecz, J.
2
Gedeon, A.
2
Lower, K.
2
Partington, M.
2
Paton, J.
2
Phillips, H.
.
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Subject
12
Amino Acid Sequence
9
Female
9
Mice
7
Pedigree
6
Base Sequence
5
Mutation
5
Sequence Homology, Amino Acid
4
Hela Cells
4
Intellectual Disability
4
Sequence Alignment
.
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Date issued
10
2000 - 2010
5
1995 - 1999