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Results 11-20 of 27 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2004
Glycogen branching enzyme (GBE1) mutation causing equine glycogen storage disease IV
Ward, T.
;
Valberg, S.
;
Adelson, D.
;
Abbey, C.
;
Binns, M.
;
Mickelson, J.
2001
Peptide insertions in domain 4 of hbc, the shared signalling receptor subunit for GM-CSF, IL3 and IL5, induce ligand-independent activation
Jones, K.
;
Bagley, C.
;
Butcher, C.
;
Barry, S.
;
Vadas, M.
;
D'Andrea, R.
2007
Cro’s role in the CI–Cro bistable switch is critical for λ’s transition from lysogeny to lytic development
Schubert, R.
;
Dodd, I.
;
Egan, J.
;
Shearwin, K.
2004
Role of N- and C-terminal residues of insulin-like growth factor (IGF)-binding protein-3 in regulating IGF complex formation and receptor activation
Yan, X.
;
Forbes, B.
;
McNeil, K.
;
Baxter, R.
;
Firth, S.
2009
Thioredoxin reductase is essential for protection of neisseria gonorrhoeae against killing by nitric oxide and for bacterial growth during interaction with cervical epithelial cells
Potter, A.
;
Kidd, S.
;
Edwards, J.
;
Falsetta, M.
;
Apicella, M.
;
Jennings, M.
;
McEwan, A.
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.
2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tarda
Gedeon, A.
;
Tiller, G.
;
Le Merrer, M.
;
Heuertz, S.
;
Tranebjaerg, L.
;
Chitayat, D.
;
Robertson, S.
;
Glass, I.
;
Savarirayan, R.
;
Cole, W.
;
Rimoin, D.
;
Kousseff, B.
;
Ohashi, H.
;
Zabel, B.
;
Munnich, A.
;
Gecz, J.
;
Mulley, J.
2001
Neuronal sodium-channel a1-subunit mutations in generalized epilepsy with febrile seizures plus
Wallace, R.
;
Scheffer, I.
;
Barnett, S.
;
Richards, M.
;
Dibbens, L.
;
Desai, R.
;
Lerman-Sagie, T.
;
Lev, D.
;
Mazarib, A.
;
Brand, N.
;
Ben-Zeev, B.
;
Goikhman, I.
;
Singh, R.
;
Kremmidiotis, G.
;
Gardner, A.
;
Sutherland, G.
;
George Jr., A.
;
Mulley, J.
;
Berkovic, S.
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.
Discover
Author
6
Mulley, J.
4
Scheffer, I.
3
Berkovic, S.
3
Gecz, J.
3
Gedeon, A.
3
Sutherland, G.
2
Apicella, M.
2
Dibbens, L.
2
et al.
2
Jennings, M.
.
next >
Subject
20
Amino Acid Sequence
17
Humans
15
Animals
11
Base Sequence
10
Mice
8
Protein Structure, Tertiary
7
Female
7
Protein Binding
7
Sequence Homology, Amino Acid
6
Male
.
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