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Issue Date
Title
Author(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.
1998
Haemolytic-uraemic syndrome outbreak caused by Escherichia coli O111:H-: clinical outcomes
Henning, P.
;
Tham, E.
;
Martin, A.
;
Beare, T.
;
Jureidini, K.
2019
The transgenerational effects of oocyte mitochondrial supplementation
St John, J.
;
Makanji, Y.
;
Johnson, J.
;
Tsai, T.-S.
;
Lagondar, S.
;
Rodda, F.
;
Sun, X.
;
Pangestu, M.
;
Chen, P.
;
Temple-Smith, P.
2000
Molecular cloning and characterisation of GPR74 a novel G-protein coupled receptor closest related to the Y-receptor family
Parker, R.
;
Copeland, N.
;
Eyre, H.
;
Liu, M.
;
Gilbert, D.
;
Crawford, J.
;
Couzens, M.
;
Sutherland, G.
;
Jenkins, N.
;
Herzog, H.
2017
Targeted insertion of an anti-CD2 monoclonal antibody transgene into the GGTA1 locus in pigs using FokI-dCas9
Nottle, M.
;
Salvaris, E.
;
Fisicaro, N.
;
McIlfatrick, S.
;
Vassiliev, I.
;
Hawthorne, W.
;
O'Connell, P.
;
Brady, J.
;
Lew, A.
;
Cowan, P.
2014
Modifications of human growth differentiation factor 9 to improve the generation of embryos from low competence oocytes
Li, J.
;
Sugimura, S.
;
Mueller, T.
;
White, M.
;
Martin, G.
;
Ritter, L.
;
Liang, X.
;
Gilchrist, R.
;
Mottershead, D.
2016
Prenatal fish oil supplementation and allergy: 6-year follow-up of a randomized controlled trial
Best, K.P.
;
Sullivan, T.
;
Palmer, D.
;
Gold, M.
;
Kennedy, D.J.
;
Martin, J.
;
Makrides, M.
2013
A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome
Buchovecky, C.
;
Turley, S.
;
Brown, H.
;
Kyle, S.
;
McDonald, J.
;
Liu, B.
;
Pieper, A.
;
Huang, W.
;
Katz, D.
;
Russell, D.
;
Shendure, J.
;
Justice, M.
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.
2015
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.
Jolly, L.
;
Nguyen, L.
;
Domingo, D.
;
Sun, Y.
;
Barry, S.
;
Hancarova, M.
;
Plevova, P.
;
Vlckova, M.
;
Havlovicova, M.
;
Kalscheuer, V.
;
Graziano, C.
;
Pippucci, T.
;
Bonora, E.
;
Sedlacek, Z.
;
Gecz, J.
Discover
Author
13
Hopwood, J.
10
Gecz, J.
9
Sutherland, G.
6
et al.
6
Jolly, L.
6
Makrides, M.
5
Gilchrist, R.
5
Shoubridge, C.
4
Barry, S.
4
Byers, S.
.
next >
Subject
62
Male
59
Humans
42
Mice
23
Pregnancy
17
Mutation
16
Disease Models, Animal
15
Molecular Sequence Data
13
Amino Acid Sequence
13
Pedigree
12
Mice, Inbred C57BL
.
next >
Date issued
43
2010 - 2019
40
2000 - 2009
17
1995 - 1999