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Results 1-10 of 24 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
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.
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.
2014
Aberrant GDF9 expression and activation are associated with common human ovarian disorders
Simpson, C.
;
Robertson, D.
;
Al-Musawi, S.
;
Heath, D.
;
McNatty, K.
;
Ritter, L.
;
Mottershead, D.
;
Gilchrist, R.
;
Harrison, C.
;
Stanton, P.
2015
p84 forms a negative regulatory complex with p110γ to control PI3Kγ signalling during cell migration
Turvey, M.
;
Klingler-Hoffmann, M.
;
Hoffmann, P.
;
McColl, S.
2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability
Huang, L.
;
Jolly, L.
;
Willis-Owen, S.
;
Gardner, A.
;
Sharma, R.
;
Douglas, E.
;
Shoubridge, C.
;
Wieczorek, D.
;
Tzschach, A.
;
Cohen, M.
;
Hackett, A.
;
Field, M.
;
Froyen, G.
;
Hu, H.
;
Haas, S.
;
Ropers, H.
;
Kalscheuer, V.
;
Corbett, M.
;
Gecz, J.
1995
Expression of bacterial cysteine biosynthesis genes in transgenic mice and sheep: Toward a new in vivo amino acid biosynthesis pathway and improved wool growth
Bawden, C.
;
Sivaprasad, A.
;
Verma, P.
;
Walker, S.
;
Rogers, G.
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.
2010
Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly
Giannandrea, M.
;
Bianchi, V.
;
Mignogna, M.
;
Sirri, A.
;
Carrabino, S.
;
D'Elia, E.
;
Vecellio, M.
;
Russo, S.
;
Cogliati, F.
;
Larizza, L.
;
Ropers, H.
;
Tzschach, A.
;
Kalscheuer, V.
;
Oehl-Jaschkowitz, B.
;
Skinner, C.
;
Schwartz, C.
;
Gecz, J.
;
Van Esch, H.
;
Raynaud, M.
;
Chelly, J.
;
et al.
2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance
Tischfield, M.
;
Baris, H.
;
Wu, C.
;
Rudolph, G.
;
van Maldergem, L.
;
He, W.
;
Chan, W.
;
Andrews, C.
;
Demer, J.
;
Robertson, R.
;
Mackey, D.
;
Ruddle, J.
;
Bird, T.
;
Gottlob, I.
;
Pieh, C.
;
Traboulsi, E.
;
Pomeroy, S.
;
Hunter, D.
;
Soul, J.
;
Newlin, A.
;
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.
Discover
Author
5
Gecz, J.
5
Mulley, J.
4
et al.
3
Shaw, M.
3
Sutherland, G.
2
Berkovic, S.
2
Corbett, M.
2
Gardner, A.
2
Gedeon, A.
2
Gilchrist, R.
.
next >
Subject
24
Animals
18
Amino Acid Sequence
13
Male
10
Mutation
8
Base Sequence
7
Pedigree
6
Intellectual Disability
6
Sequence Alignment
5
X Chromosome
4
Brain
.
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Date issued
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2000 - 2009
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1995 - 1999