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Results 1-10 of 18 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2013
Functional studies of the yeast Med5, Med15 and Med16 mediator tail subunits
Larsson, M.
;
Uvell, H.
;
Sandstrom, J.
;
Ryden, P.
;
Selth, L.
;
Bjorklund, S.
;
Mantovani, R.
2012
CDP-diacylglycerol synthetase-controlled phosphoinositide availability limits VEGFA signaling and vascular morphogenesis
Pan, W.
;
Pham, V.
;
Stratman, A.
;
Castranova, D.
;
Kamei, M.
;
Kidd, K.
;
Lo, B.
;
Shaw, K.
;
Torres-Vazquez, J.
;
Mikelis, C.
;
Gutkind, J.
;
Davis, G.
;
Weinstein, B.
2013
The genomic landscape of hypodiploid acute lymphoblastic leukemia
To, L.
2016
Ampullary cancers harbor ELF3 tumor suppressor gene mutations and exhibit frequent WNT dysregulation
Gingras, M.
;
Chang, D.
;
Donehower, L.
;
Covington, K.
;
Gill, A.
;
Ittmann, M.
;
Creighton, C.
;
Johns, A.
;
Shinbrot, E.
;
Dewal, N.
;
Fisher, W.
;
Pilarsky, C.
;
Grützmann, R.
;
Overman, M.
;
Jamieson, N.
;
Van Buren, G.
;
Drummond, J.
;
Walker, K.
;
Hampton, O.
;
Xi, L.
;
et al.
2014
Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease
Newman, M.
;
Wilson, L.
;
Verdile, G.
;
Lim, A.
;
Khan, I.
;
Nik, S.
;
Pursglove, S.
;
Chapman, G.
;
Martins, R.
;
Lardelli, M.
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.
2011
Conservation of plastid sequences in the plant nuclear genome for millions of years facilitates endosymbiotic evolution
Rousseau, M.
;
Ayliffe, M.
;
Timmis, J.
2010
Poor prognosis in familial acute myeloid leukaemia with combined biallelic CEBPA mutations and downstream events affecting the ATM, FLT3 and CDX2 genes
Carmichael, C.
;
Wilkins, E.
;
Bengtsson, H.
;
Horwitz, M.
;
Speed, T.
;
Vincent, P.
;
Young, G.
;
Hahn, C.
;
Escher, J.
;
Scott, H.
Discover
Author
5
et al.
3
Gecz, J.
2
Christodoulou, J.
2
Haan, E.
2
Liang, W.
2
Timmis, J.
2
Zhang, D.
1
Abdelhamed, Z.
1
Afawi, Z.
1
Al Raisi, Z.
.
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Subject
15
Molecular Sequence Data
11
Humans
7
Animals
5
Amino Acid Sequence
5
Female
5
Male
5
Mice
5
Pedigree
4
Genes, Plant
4
Phylogeny
.
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Date issued
1
2016
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2014
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2013
3
2012
4
2011
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2010