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Results 1-10 of 13 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2007
Kit signaling is essential for development and maintenance of interstitial cells of Cajal and electrical rhythmicity in the embryonic gastrointestinal tract
Spencer, E.
;
Ro, S.
;
Bayguinov, Y.
;
Sanders, K.
;
Ward, 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.
2001
Gene structure, alternative splicing, and chromosomal localization of pro-apoptotic Bcl-2 relative Bim
Bouillet, P.
;
Zhang, L.
;
Huang, D.
;
Webb, G.
;
Bottema, C.
;
Shore, P.
;
Eyre, H.
;
Sutherland, G.
;
Adams, J.
2005
Mutation of the androgen receptor causes oncogenic transformation of the prostate
Han, G.
;
Buchanan, G.
;
Ittmann, M.
;
Harris, J.
;
Yu, X.
;
DeMayo, F.
;
Tilley, W.
;
Greenberg, N.
2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation
Burdon, K.
;
McKay, J.
;
Sale, M.
;
Russell-Eggitt, I.
;
Mackey, D.
;
Wirth, G.
;
Elder, J.
;
Nicoll, A.
;
Clarke, M.
;
FitzGerald, L.
;
Stankovich, J.
;
Shaw, M.
;
Sharma, S.
;
Gajovic, S.
;
Gruss, P.
;
Ross, S.
;
Thomas, P.
;
Voss, A.
;
Thomas, T.
;
Gecz, J.
;
et al.
2003
Mouse sulphamidase gene: characterization of the promoter region of the gene and expression in mouse tissues
Costanzi, E.
;
Beccari, T.
;
Aisa, M.
;
Tiribuzi, R.
;
Hopwood, J.
;
Orlacchio, A.
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.
2004
LGI1 mutations in temporal lobe epilepsies
Berkovic, S.
;
Izzillo, P.
;
McMahon, J.
;
Harkin, L.
;
McIntosh, A.
;
Phillips, H.
;
Briellmann, R.
;
Wallace, R.
;
Mazarib, A.
;
Neufeld, M.
;
Korczyn, A.
;
Scheffer, I.
;
Mulley, J.
2001
TTYH2, a human homologue of the Drosophila melanogaster gene tweety, is located on 17q24 and upregulated in renal cell carcinoma
Rae, F.
;
Hooper, J.
;
Eyre, H.
;
Sutherland, G.
;
Nicol, D.
;
Clements, J.
Discover
Author
4
Sutherland, G.
3
Mulley, J.
3
Shaw, M.
2
et al.
2
Eyre, H.
2
Gecz, J.
2
Gedeon, A.
2
Lower, K.
2
Ross, S.
2
Scheffer, I.
.
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Subject
13
Animals
10
Amino Acid Sequence
10
Humans
7
Female
5
Sequence Alignment
4
Base Sequence
4
Mutation
4
Pedigree
3
In Situ Hybridization, Fluorescence
3
Intellectual Disability
.
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