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Results 1-10 of 12 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2005
Cytoplasmic ATP-sensing domains regulate gating of skeletal muscle ClC-1 chloride channels
Bennetts, B.
;
Rychkov, G.
;
Ng, H.
;
Morton, C.
;
Stapleton, D.
;
Parker, M.
;
Cromer, B.
2007
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation
Tarpey, P.
;
Raymond, F.
;
Nguyen, L.
;
Rodriguez, J.
;
Hackett, A.
;
Vandeleur, L.
;
Smith, R.
;
Shoubridge, C.
;
Edkins, S.
;
Stevens, C.
;
O'Meara, S.
;
Tofts, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Halliday, K.
;
Hills, K.
;
Jones, D.
;
Mironenko, T.
;
Perry, J.
;
et al.
1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
Gedeon, A.
;
Colley, A.
;
Jamieson, R.
;
Thompson, E.
;
Rogers, J.
;
Sillence, D.
;
Tiller, G.
;
Mulley, J.
;
Gecz, J.
2010
The structure of the talin/integrin complex at a lipid bilayer: an NMR and MD simulation study
Kalli, A.
;
Wegener, K.
;
Goult, B.
;
Anthis, N.
;
Campbell, I.
;
Sansom, M.
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.
1999
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM
Friend, K.
;
Crimmins, D.
;
Phan, T.
;
Sue, C.
;
Colley, A.
;
Fung, V.
;
Morris, J.
;
Sutherland, G.
;
Richards, R.
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.
1997
Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean Fever
Aksentijevich, I.
;
Centola, M.
;
Deng, Z.
;
Sood, R.
;
Balow, J.
;
Wood, G.
;
Zaks, N.
;
Mansfield, E.
;
Chen, X.
;
Eisenberg, S.
;
Vedula, A.
;
Shafran, N.
;
Raben, N.
;
Pras, E.
;
Pras, M.
;
Kastner, D.
;
Blake, T.
;
Baxevanis, A.
;
Robbins, C.
;
Krizman, D.
;
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.
2012
HIV-1 infection of human macrophages directly induces viperin which inhibits viral production
Nasr, N.
;
Maddocks, S.
;
Turville, S.
;
Harman, A.
;
Woolger, N.
;
Helbig, K.
;
Wilkinson, J.
;
Bye, C.
;
Wright, T.
;
Rambukwelle, D.
;
Donaghy, H.
;
Beard, M.
;
Cunningham, A.
Discover
Author
2
Colley, A.
2
et al.
2
Gecz, J.
2
Gedeon, A.
2
Mulley, J.
2
Sutherland, G.
1
Aksentijevich, I.
1
Anthis, N.
1
Bagley, C.
1
Balow, J.
.
next >
Subject
12
Amino Acid Sequence
10
Humans
6
Animals
4
Female
4
Male
4
Mutagenesis, Site-Directed
4
Pedigree
4
Protein Binding
4
Protein Structure, Tertiary
3
DNA Mutational Analysis
.
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Date issued
2
2010 - 2012
7
2000 - 2009
3
1997 - 1999