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Results 1-10 of 104 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1995
Luteinizing hormone/chorionic gonadotropin bioactivity in the common marmoset (Callithrix jacchus) is due to a chorionic gonadotropin molecule with a structure intermediate between human chorionic gonadotropin and human luteinizing hormone.
Simula, A.
;
Amato, F.
;
Faast, R.
;
Lopata, A.
;
Berka, J.
;
Norman, R.
1997
Most germ-line mutations in the nevoid basal cell carcinoma syndrome lead to a premature termination of the PATCHED protein, and no genotype-phenotype correlations are evident
Wicking, C.
;
Shanley, S.
;
Smyth, I.
;
Gillies, S.
;
Negus, K.
;
Graham, S.
;
Suthers, G.
;
Haites, N.
;
Edwards, M.
;
Wainwright, B.
;
Chenevix Trench, G.
1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24
Phillips, H.
;
Scheffer, I.
;
Crossland, K.
;
Bhatia, K.
;
Fish, D.
;
Marsden, C.
;
Howell, S.
;
Stephenson, J.
;
Tolmie, J.
;
Plazzi, G.
;
Eeg-Olofsson, O.
;
Singh, R.
;
Lopes-Cendes, I.
;
Andermann, E.
;
Berkovic, S.
;
Mulley, J.
2004
Inhibition of generation of cytotoxic T lymphocyte activity by a CCL19/macrophage inflammatory protein (MIP)-3beta antagonist
Pilkington, K.
;
Clark-Lewis, I.
;
McColl, S.
2004
Expression of rat I-TAC/CXCL11/SCYA11 during central nervous system inflammation: comparison with other CXCR3 ligands
McColl, S.
;
Mahalingam, S.
;
Staykova, M.
;
Tylaska, L.
;
Fisher, K.
;
Strick, C.
;
Gladue, R.
;
Neote, K.
;
Willenborg, D.
2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitus
Raymond, F.
;
Tarpey, P.
;
Edkins, S.
;
Tofts, C.
;
O'Meara, S.
;
Teague, J.
;
Butler, A.
;
Stevens, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Dicks, E.
;
Gray, K.
;
Harrison, R.
;
Hills, K.
;
Hinton, J.
;
Jones, D.
;
Menzies, A.
;
Perry, J.
;
Raine, K.
;
et al.
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.
1996
bcl-w, a novel member of the bcl-2 family, promotes cell survival
Gibson, L.
;
Holmgreen, S.
;
Huang, D.
;
Bernand, O.
;
Copeland, N.
;
Jenkins, N.
;
Sutherland, G.
;
Baker, E.
;
Adams, J.
;
Cory, 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.
2005
Ancient DNA from the first European farmers in 7500-year-old Neolithic sites
Haak, W.
;
Forster, P.
;
Bramanti, B.
;
Matsumura, S.
;
Brandt, G.
;
Tanzer, M.
;
Villems, R.
;
Renfrew, C.
;
Gronenborn, D.
;
Alt, K.
;
Burger, J.
Discover
Author
21
Gecz, J.
17
Sutherland, G.
15
Mulley, J.
14
et al.
10
Berkovic, S.
10
Scheffer, I.
8
Haan, E.
7
Gedeon, A.
6
Dibbens, L.
6
Wallace, R.
.
next >
Subject
70
Male
62
Amino Acid Sequence
51
Base Sequence
48
Animals
36
Pedigree
33
Mutation
24
Mice
20
Adult
20
Sequence Homology, Amino Acid
18
Sequence Analysis, DNA
.
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Date issued
27
2010 - 2015
45
2000 - 2009
32
1995 - 1999