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Results 1-10 of 18 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2017
A genetic screen for impaired systemic RNAi highlights the crucial role of DICER-LIKE 2
Taochy, C.
;
Gursanscky, N.
;
Cao, J.
;
Fletcher, S.
;
Dressel, U.
;
Mitter, N.
;
Tucker, M.
;
Koltunow, A.
;
Bowman, J.
;
Vaucheret, H.
;
Carroll, B.
2017
Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signalling
Hughes, J.
;
Dawson, R.
;
Tea, M.
;
McAninch, D.
;
Piltz, S.
;
Jackson, D.
;
Stewart, L.
;
Ricos, M.
;
Dibbens, L.
;
Harvey, N.
;
Thomas, P.
2017
NAD deficiency, congenital malformations, and niacin supplementation
Shi, H.
;
Enriquez, A.
;
Rapadas, M.
;
Martin, E.
;
Wang, R.
;
Moreau, J.
;
Lim, C.
;
Szot, J.
;
Ip, E.
;
Hughes, J.
;
Sugimoto, K.
;
Humphreys, D.
;
McInerney-Leo, A.
;
Leo, P.
;
Maghzal, G.
;
Halliday, J.
;
Smith, J.
;
Colley, A.
;
Mark, P.
;
Collins, F.
;
et al.
2017
Two SUMO proteases SUMO PROTEASE RELATED TO FERTILITY1 and 2 are required for fertility in arabidopsis
Liu, L.
;
Jiang, Y.
;
Zhang, X.
;
Wang, X.
;
Wang, Y.
;
Han, Y.
;
Coupland, G.
;
Jin, J.
;
Searle, I.
;
Fu, Y.
;
Chen, F.
2017
Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan Anemia patient
Venugopal, P.
;
Moore, S.
;
Lawrence, D.
;
George, A.
;
Hannan, R.
;
Bray, S.
;
To, L.
;
D Andrea, R.
;
Feng, J.
;
Tirimacco, A.
;
Yeoman, A.
;
Young, C.
;
Fine, M.
;
Schreiber, A.
;
Hahn, C.
;
Barnett, C.
;
Saxon, B.
;
Scott, H.
2017
Structure aided design of a Neu5Gc specific lectin
Day, C.
;
Paton, A.
;
Higgins, M.
;
Shewell, L.
;
Jen, F.
;
Schulz, B.
;
Herdman, B.
;
Paton, J.
;
Jennings, M.
2017
A method for next-generation sequencing of paired diagnostic and remission Samples to detect mitochondrial DNA mutations associated with leukemia
Pagani, I.S.
;
Kok, C.H.
;
Saunders, V.A.
;
Van der Hoek, M.B.
;
Heatley, S.L.
;
Schwarer, A.P.
;
Hahn, C.N.
;
Hughes, T.P.
;
White, D.L.
;
Ross, D.M.
2017
Regulation of Orai1/STIM1 mediated ICRAC by intracellular pH
Gavriliouk, D.
;
Scrimgeour, N.
;
Grigoryev, S.
;
Ma, L.
;
Zhou, F.
;
Barritt, G.
;
Rychkov, G.
2017
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Stessman, H.
;
Xiong, B.
;
Coe, B.
;
Wang, T.
;
Hoekzema, K.
;
Fenckova, M.
;
Kvarnung, M.
;
Gerdts, J.
;
Trinh, S.
;
Cosemans, N.
;
Vives, L.
;
Lin, J.
;
Turner, T.
;
Santen, G.
;
Ruivenkamp, C.
;
Kriek, M.
;
Van Haeringen, A.
;
Aten, E.
;
Friend, K.
;
Liebelt, J.
;
et al.
2017
Defective pollen wall 2 (Dpw2) encodes an acyl transferase required for rice pollen development
Xu, D.
;
Shi, J.
;
Rautengarten, C.
;
Yang, L.
;
Qian, X.
;
Uzair, M.
;
Zhu, L.
;
Luo, Q.
;
An, G.
;
Waßmann, F.
;
Schreiber, L.
;
Heazlewood, J.
;
Scheller, H.
;
Hu, J.
;
Zhang, D.
;
Liang, W.
Discover
Author
4
et al.
2
Hughes, J.
2
Liang, W.
2
McAninch, D.
2
Paton, A.
2
Paton, J.
2
Thomas, P.
2
Zhang, D.
1
Allerdice, S.L.
1
An, G.
.
next >
Subject
13
Humans
6
Animals
6
Female
6
Male
5
Phenotype
4
Mice
3
Cell Line, Tumor
3
Epilepsy
3
Intellectual Disability
3
Mice, Knockout
.
next >