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Results 21-30 of 41 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2013
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, L.
;
de Vries, B.
;
Donatello, S.
;
Heron, S.
;
Hodgson, B.
;
Chintawar, S.
;
Crompton, D.
;
Hughes, J.
;
Bellows, S.
;
Klein, K.
;
Callenbach, P.
;
Corbett, M.
;
Gardner, A.
;
Kivity, S.
;
Iona, X.
;
Regan, B.
;
Weller, C.
;
Crimmins, D.
;
O'Brien, T.
;
Guerrero-Lopez, R.
;
et al.
2002
Truncation of the GABAA-receptor γ2 subunit in a family with generalized epilepsy with febrile seizures plus
Harkin, L.
;
Bowser, D.
;
Dibbens, L.
;
Singh, R.
;
Phillips, F.
;
Wallace, R.
;
Richards, M.
;
Williams, D.
;
Mulley, J.
;
Berkovic, S.
;
Scheffer, I.
;
Petrou, S.
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.
2009
Location, Location, Location! Monotremes Provide Unique Insights into the Evolution of Sex Chromosome Silencing in Mammals
Daish, T.
;
Grutzner, F.
2004
A functional autoantibody in narcolepsy
Smith, A.
;
Jackson, M.
;
Neufing, P.
;
McEvoy, R.
;
Gordon, T.
2004
Post-meiotic gene products as targets for male contraception
Ivell, R.
;
Danner, S.
;
Fritsch, M.
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.
2006
Cellular origins of testicular dysgenesis in rats exposed in utero to di(n-butyl) phthalate
Mahood, K.
;
McKinnell, C.
;
Walker, M.
;
Hallmark, N.
;
Scott, H.
;
Fisher, J.
;
Rivas, A.
;
Hartung, S.
;
Ivell, R.
;
Mason, J.
;
Sharpe, R.
Discover
Author
6
Paton, J.
5
et al.
5
Mulley, J.
4
Ivell, R.
4
Paton, A.
4
Thomas, P.
3
Berkovic, S.
3
Dibbens, L.
3
Grutzner, F.
3
Scheffer, I.
.
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Subject
26
Female
22
Mice
9
Molecular Sequence Data
8
Amino Acid Sequence
8
Middle Aged
7
Mice, Inbred BALB C
7
Mutation
7
Transcription Factors
6
Adult
6
Aged
.
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Date issued
15
2010 - 2019
25
2000 - 2009
1
1982 - 1989