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Results 11-20 of 30 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2019
Combining BH3-mimetics to target both BCL-2 and MCL1 has potent activity in pre-clinical models of acute myeloid leukemia
Moujalled, D.M.
;
Pomilio, G.
;
Ghiurau, C.
;
Ivey, A.
;
Salmon, J.
;
Rijal, S.
;
Macraild, S.
;
Zhang, L.
;
Teh, T.C.
;
Tiong, I.S.
;
Lan, P.
;
Chanrion, M.
;
Claperon, A.
;
Rocchetti, F.
;
Zichi, A.
;
Kraus-Berthier, L.
;
Wang, Y.
;
Halilovic, E.
;
Morris, E.
;
Colland, F.
;
et al.
2015
Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene
Ishibashi, M.
;
Manning, E.
;
Shoubridge, C.
;
Krecsmarik, M.
;
Hawkins, T.
;
Giacomotto, J.
;
Zhao, T.
;
Mueller, T.
;
Bader, P.
;
Cheung, S.
;
Stankiewicz, P.
;
Bain, N.
;
Hackett, A.
;
Reddy, C.
;
Mechaly, A.
;
Peers, B.
;
Wilson, S.
;
Lenhard, B.
;
Bally-Cuif, L.
;
Gecz, J.
;
et al.
2016
Choline kinase alpha as an androgen receptor chaperone and prostate cancer therapeutic target
Asim, M.
;
Massie, C.
;
Orafidiya, F.
;
PĂ©rtega-Gomes, N.
;
Warren, A.
;
Esmaeili, M.
;
Selth, L.
;
Zecchini, H.
;
Luko, K.
;
Qureshi, A.
;
Baridi, A.
;
Menon, S.
;
Madhu, B.
;
Escriu, C.
;
Lyons, S.
;
Vowler, S.
;
Zecchini, V.
;
Shaw, G.
;
Hessenkemper, W.
;
Russell, R.
;
et al.
2013
Identification Of KLHL41 mutations implicates BTB-Kelch-Mediated Ubiquitination as an alternate pathway to myofibrillar disruption in nemaline myopathy
Gupta, V.
;
Ravenscroft, G.
;
Shaheen, R.
;
Todd, E.
;
Swanson, L.
;
Shiina, M.
;
Ogata, K.
;
Hsu, C.
;
Clarke, N.
;
Darras, B.
;
Farrar, M.
;
Hashem, A.
;
Manton, N.
;
Muntoni, F.
;
North, K.
;
Sandaradura, S.
;
Nishino, I.
;
Hayashi, Y.
;
Sewry, C.
;
Thompson, E.
;
et al.
2012
Glucokinase links Kruppel-like factor 6 to the regulation of hepatic insulin sensitivity in nonalcoholic fatty liver disease
Bechmann, L.
;
Gastaldelli, A.
;
Vetter, D.
;
Patman, G.
;
Pascoe, L.
;
Hannivoort, R.
;
Lee, U.
;
Fiel, I.
;
Munoz, U.
;
Ciociaro, D.
;
Lee, Y.
;
Buzzigoli, E.
;
Miele, L.
;
Hui, K.
;
Bugianesi, E.
;
Burt, A.
;
Day, C.
;
Mari, A.
;
Agius, L.
;
Walker, M.
;
et al.
2016
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
Hu, H.
;
Haas, S.
;
Chelly, J.
;
Van Esch, H.
;
Raynaud, M.
;
De Brouwer, A.
;
Weinert, S.
;
Froyen, G.
;
Frints, S.
;
Laumonnier, F.
;
Zemojtel, T.
;
Love, M.
;
Richard, H.
;
Emde, A.
;
Bienek, M.
;
Jensen, C.
;
Hambrock, M.
;
Fischer, U.
;
Langnick, C.
;
Feldkamp, M.
;
et al.
2013
Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome
Aoki, Y.
;
Niihori, T.
;
Banjo, T.
;
Okamoto, N.
;
Mizuno, S.
;
Kurosawa, K.
;
Ogata, T.
;
Takada, F.
;
Yano, M.
;
Ando, T.
;
Hoshika, T.
;
Barnett, C.
;
Ohashi, H.
;
Kawame, H.
;
Hasegawa, T.
;
Okutani, T.
;
Nagashima, T.
;
Hasegawa, S.
;
Funayama, R.
;
Nagashima, T.
;
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.
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.
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.
Discover
Author
4
Hughes, J.
3
Gecz, J.
2
Babic, M.
2
Chelly, J.
2
Chong, C.
2
Corbett, M.
2
Gardner, A.
2
Hahn, C.
2
Heron, S.
2
Hodgson, B.
.
next >
Subject
23
Mice
22
Female
10
Child
10
Mutation
9
Child, Preschool
8
Adult
8
Pedigree
7
Adolescent
6
Brain
6
Disease Models, Animal
.
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Date issued
4
2019
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2018
3
2017
4
2016
1
2015
1
2014
4
2013
5
2012
3
2011
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2010
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