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Results 21-30 of 51 (Search time: 0.006 seconds).
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Issue Date
Title
Author(s)
2013
Regulation of vascular leak and recovery from ischemic injury by general and VE-cadherin-restricted miRNA antagonists of miR-27
Young, J.
;
Ting, K.
;
Li, J.
;
Moller, T.
;
Dunn, L.
;
Lu, Y.
;
Moses, J.
;
Prado-Lourenco, L.
;
Khachigian, L.
;
Ng, M.
;
Gregory, P.
;
Goodall, G.
;
Tsykin, A.
;
Lichtenstein, I.
;
Hahn, C.
;
Tran, N.
;
Shackel, N.
;
Kench, J.
;
McCaughan, G.
;
Vadas, M.
;
et al.
2016
A syntenic cross species aneuploidy genetic screen links RCAN1 expression to β-Cell mitochondrial dysfunction in type 2 diabetes
Peiris, H.
;
Duffield, M.D.
;
Fadista, J.
;
Jessup, C.F.
;
Kashmir, V.
;
Genders, A.J.
;
McGee, S.L.
;
Martin, A.M.
;
Saiedi, M.
;
Morton, N.
;
Carter, R.
;
Cousin, M.A.
;
Kokotos, A.C.
;
Oskolkov, N.
;
Volkov, P.
;
Hough, T.A.
;
Fisher, E.M.C.
;
Tybulewicz, V.L.J.
;
Busciglio, J.
;
Coskun, P.E.
;
et al.
;
Scott, H.S.
2015
Progesterone receptor modulates ERα action in breast cancer
Mohammed, H.
;
Russell, I.
;
Stark, R.
;
Rueda, O.
;
Hickey, T.
;
Tarulli, G.
;
Serandour, A.
;
Birrell, S.
;
Bruna, A.
;
Saadi, A.
;
Menon, S.
;
Hadfield, J.
;
Pugh, M.
;
Raj, G.
;
Brown, G.
;
D'Santos, C.
;
Robinson, J.
;
Silva, G.
;
Launchbury, R.
;
Perou, C.
;
et al.
2012
Death adder envenoming causes neurotoxicity not reversed by antivenom - Australian snakebite project (ASP-16)
Johnston, C.
;
O'Leary, M.
;
Brown, S.
;
Currie, B.
;
Halkidis, L.
;
Whitaker, R.
;
Close, B.
;
Isbister, G.
;
Nagree, Y.
;
Ker, F.
;
Greene, S.
;
Taylor, M.
;
Macrokanis, C.
;
Wilke, G.
;
Coulson, A.
;
Barnes, C.
;
Bonni, R.
;
Whitake, R.
;
Halkidis, L.
;
Isbiste, G.
;
et al.
;
de Silva, J.
2013
Distinctive expansion of potential virulence genes in the genome of the oomycete fish pathogen Saprolegnia parasitica
Jiang, R.
;
de Bruijn, I.
;
Haas, B.
;
Belmonte, R.
;
Löbach, L.
;
Christie, J.
;
van den Ackerveken, G.
;
Bottin, A.
;
Bulone, V.
;
Díaz-Moreno, S.
;
Dumas, B.
;
Fan, L.
;
Gaulin, E.
;
Govers, F.
;
Grenville-Briggs, L.
;
Horner, N.
;
Levin, J.
;
Mammella, M.
;
Meijer, H.
;
Morris, P.
;
et al.
;
McDowell, J.
2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Heron, S.
;
Grinton, B.
;
Kivity, S.
;
Afawi, Z.
;
Zuberi, S.
;
Hughes, J.
;
Pridmore, C.
;
Hodgson, B.
;
Iona, X.
;
Sadleir, L.
;
Pelekanos, J.
;
Herlenius, E.
;
Goldberg-Stern, H.
;
Bassan, H.
;
Haan, E.
;
Korczyn, A.
;
Gardner, A.
;
Corbett, M.
;
Gecz, J.
;
Thomas, P.
;
et al.
2011
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma
Khan, K.
;
Rudkin, A.
;
Parry, D.
;
Burdon, K.
;
McKibbin, M.
;
Logan, C.
;
Abdelhamed, Z.
;
Muecke, J.
;
Fernandez-Fuentes, N.
;
Laurie, K.
;
Shires, M.
;
Fogarty, R.
;
Carr, I.
;
Poulter, J.
;
Morgan, J.
;
Mohamed, M.
;
Jafri, H.
;
Raashid, Y.
;
Meng, N.
;
Piseth, H.
;
et al.
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
Mutations in MAP3K1 cause 46,XY disorders of sex development and implicate a common signal transduction pathway in human testis determination
Pearlman, A.
;
Loke, J.
;
Le Caignec, C.
;
White, S.
;
Chin, L.
;
Friedman, A.
;
Warr, N.
;
Willan, J.
;
Brauer, D.
;
Farmer, C.
;
Brooks, E.
;
Oddoux, C.
;
Riley, B.
;
Shajahan, S.
;
Camerino, G.
;
Homfray, T.
;
Crosby, A.
;
Couper, J.
;
David, A.
;
Greenfield, A.
;
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.
Discover
Author
4
Hughes, J.
3
Gecz, J.
3
Hahn, C.
2
Amat, J.
2
Babic, M.
2
Baker, A.
2
Burdon, K.
2
Chelly, J.
2
Chong, C.
2
Corbett, M.
.
next >
Subject
39
Humans
32
Mice
27
Male
22
Female
12
Mutation
9
Mice, Inbred C57BL
9
Signal Transduction
7
Adult
7
Base Sequence
7
Brain
.
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Date issued
8
2017
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2016
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2015
3
2014
10
2013
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2012
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2011
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2010