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Results 11-20 of 34 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2010
A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24
Bahlo, M.
;
Jolly, L.
;
Afawi, Z.
;
Gardner, A.
;
Oliver, K.
;
Tan, S.
;
Coffey, A.
;
Mulley, J.
;
Dibbens, L.
;
Simri, W.
;
Shalata, A.
;
Kivity, S.
;
Jackson, G.
;
Berkovic, S.
;
Gecz, J.
;
Corbett, M.
2011
Tmprss3, a transmembrane serine protease deficient in human DFNB8/10 deafness, is critical for cochlear hair cell survival at the onset of hearing
Fasquelle, L.
;
Scott, H.
;
Lenoir, M.
;
Wang, J.
;
Rebillard, G.
;
Gaboyard, S.
;
Venteo, S.
;
Francois, F.
;
Masset-Bonnefont, A.
;
Antonarakis, S.
;
Neidhart, E.
;
Chabbert, C.
;
Puel, J.
;
Guipponi, M.
;
Delprat, B.
2008
Islet-1: A potentially important role for an islet cell gene in visceral fat
Li, H.
;
Heilbronn, L.
;
Hu, D.
;
Poynten, A.
;
Blackburn, M.
;
Shirkhedkar, D.
;
Kaplan, W.
;
Kriketos, A.
;
Ye, J.
;
Chisholm, D.
2010
Myc-modulated miR-9 makes more metastases
Khew-Goodall, Y.
;
Goodall, G.
2013
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, L.
;
de Vries, B.
;
Donatello, S.
;
Heron, S.
;
Hodgson, B.
;
Chintawar, S.
;
Crompton, D.
;
Hughes, J.
;
Bellows, S.
;
Klein, K.
;
Callenbach, P.
;
Corbett, M.
;
Gardner, A.
;
Kivity, S.
;
Iona, X.
;
Regan, B.
;
Weller, C.
;
Crimmins, D.
;
O'Brien, T.
;
Guerrero-Lopez, R.
;
et al.
2007
A pneumococcal MerR-like regulator and S-nitrosoglutathione reductase are required for systemic virulence
Stroeher, U.
;
Kidd, S.
;
Stafford, S.
;
Jennings, M.
;
Paton, J.
;
McEwan, A.
2006
Production and characterization of monoclonal antibodies against insulin-like growth factor type 1 receptor
Keyhanfar, M.
;
Forbes, B.
;
Cosgrove, L.
;
Wallace, J.
;
Booker, G.
2004
A functional autoantibody in narcolepsy
Smith, A.
;
Jackson, M.
;
Neufing, P.
;
McEvoy, R.
;
Gordon, T.
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
7
Paton, J.
3
et al.
3
Mulley, J.
3
Paton, A.
2
Alsharifi, M.
2
Corbett, M.
2
de Vries, B.
2
Dibbens, L.
2
Gardner, A.
2
Gecz, J.
.
next >
Subject
34
Animals
15
Male
10
Mutation
9
Mice, Inbred BALB C
8
Molecular Sequence Data
7
Amino Acid Sequence
6
Mice, Inbred C57BL
6
Middle Aged
6
Streptococcus pneumoniae
5
Adult
.
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Date issued
1
2020 - 2023
16
2010 - 2019
17
2001 - 2009