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Issue Date
Title
Author(s)
2016
TBC1D24 genotype-phenotype correlation
Balestrini, S.
;
Milh, M.
;
Castiglioni, C.
;
Lüthy, K.
;
Finelli, M.
;
Verstreken, P.
;
Cardon, A.
;
Stražišar, B.
;
Holder, J.
;
Lesca, G.
;
Mancardi, M.
;
Poulat, A.
;
Repetto, G.
;
Banka, S.
;
Bilo, L.
;
Birkeland, L.
;
Bosch, F.
;
Brockmann, K.
;
Cross, J.
;
Doummar, D.
;
et al.
2017
ProBDNF Accelerates Brain Amyloid-β Deposition and Learning and Memory Impairment in APPswePS1dE9 Transgenic Mice
Chen, J.
;
Zhang, T.
;
Jiao, S.
;
Zhou, X.
;
Zhong, J.
;
Wang, Y.
;
Liu, J.
;
Deng, J.
;
Wang, S.
;
Xu, Z.
2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity
Hirata, H.
;
McMichael, G.
;
Haan, E.
;
MacLennan, A.
;
Yap, T.
;
Nguyen, L.
;
Shaw, 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.
2013
Characterization of mutants of a highly cross-reactive calcium-binding protein from Brassica pollen for allergen-specific immunotherapy
Garmatiuk, T.
;
Swoboda, I.
;
Twardosz-Kropfmüller, A.
;
Dall’Antonia, F.
;
Keller, W.
;
Singh, M.B.
;
Bhalla, P.L.
;
Okada, T.
;
Toriyama, K.
;
Weber, M.
;
Ghannadan, M.
;
Sperr, W.R.
;
Blatt, K.
;
Valent, P.
;
Klein, B.
;
Niederberger, V.
;
Curin, M.
;
Balic, N.
;
Spitzauer, S.
;
Valenta, R.
2013
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, L.
;
de Vries, B.
;
Donatello, S.
;
Heron, S.
;
Hodgson, B.
;
Chintawar, S.
;
Crompton, D.
;
Hughes, J.
;
Bellows, S.
;
Klein, K.
;
Callenbach, P.
;
Corbett, M.
;
Gardner, A.
;
Kivity, S.
;
Iona, X.
;
Regan, B.
;
Weller, C.
;
Crimmins, D.
;
O'Brien, T.
;
Guerrero-Lopez, R.
;
et al.
2012
Identification of a novel pneumococcal vaccine antigen preferentially expressed during meningitis in mice
Mahdi, L.
;
Wang, H.
;
Van der Hoek, M.
;
Paton, J.
;
Ogunniyi, A.
2018
A Upf3b-mutant mouse model with behavioral and neurogenesis defects
Huang, L.
;
Shum, E.
;
Jones, S.
;
Lou, C.-H.
;
Dumdie, J.
;
Kim, H.
;
Roberts, A.
;
Jolly, L.
;
Espinoza, J.
;
Skarbrevik, D.
;
Phan, M.
;
Cook-Andersen, H.
;
Swerdlow, N.
;
Gecz, J.
;
Wilkinson, M.
Discover
Author
3
Gecz, J.
2
et al.
2
Jolly, L.
2
Nguyen, L.
1
Balestrini, S.
1
Balic, N.
1
Banka, S.
1
Barry, S.
1
Bellows, S.
1
Bhalla, P.L.
.
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Subject
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6
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3
Brain
3
Carrier Proteins
3
Pedigree
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Young Adult
2
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Amino Acid Sequence
2
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