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Results 21-30 of 99 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2007
Phosphorylation of StarD10 on serine 284 by casein kinase II modulates its lipid transfer activity
Olayioye, M.
;
Buchholz, M.
;
Schmid, S.
;
Schoffler, P.
;
Hoffmann, P.
;
Pomorski, T.
2003
Immunoexpression of the relaxin receptor LGR7 in breast and uterine tissues of humans and primates
Ivell, R.
;
Balvers, M.
;
Pohnke, Y.
;
Telgmann, R.
;
Bartsch, O.
;
Milde-Langosch, K.
;
Bamberger, A.
;
Einspanier, A.
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
Construction of an ~700-kb transcript map around the Familial Mediterranean Fever locus on human chromosome 16p13.3
Centola, M.
;
Chen, X.
;
Sood, R.
;
Deng, Z.
;
Aksentijevich, I.
;
Blake, T.
;
Ricke, D.
;
Chen, X.
;
Wood, G.
;
Zaks, N.
;
Richards, N.
;
Krizman, D.
;
Mansfield, E.
;
Apostolou, S.
;
Liu, J.
;
Shafran, N.
;
Vedula, A.
;
Hamon, M.
;
Cercek, A.
;
Kahan, T.
;
et al.
2008
Ribosomal stress induces processing of Mybbp1a and its translocation from the nucleolus to the nucleoplasm
Yamauchi, T.
;
Keough, R.
;
Gonda, T.
;
Ishii, S.
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.
1998
Molecular analysis of shiga toxigenic Escherichia coli O111:H proteins which react with sera from patients with hemolytic-uremic syndrome.
Voss, E.
;
Paton, A.
;
Manning, P.
;
Paton, J.
2002
New roles for old holes: Ion channel function in aquaporin-1
Yool, A.
;
Weinstein, A.
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.
Discover
Author
12
Mulley, J.
9
Sutherland, G.
9
Whitelaw, M.
8
Forbes, B.
8
Gecz, J.
7
Paton, J.
7
Wallace, J.
6
Berkovic, S.
6
Booker, G.
6
McColl, S.
.
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Subject
65
Animals
40
Sequence Homology, Amino Acid
38
Mice
26
Base Sequence
24
Female
24
Mutation
23
Male
20
Sequence Alignment
17
Transcription Factors
16
Cell Line
.
next >
Date issued
15
2010 - 2014
55
2000 - 2009
29
1995 - 1999