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Issue Date
Title
Author(s)
2013
Mechanotransduction pathways promoting tumor progression are activated in invasive human squamous cell carcinoma
Ibbetson, S.
;
Pyne, N.
;
Pollard, A.
;
Olson, M.
;
Samuel, M.
2013
Yunis-VarĂ³n Syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase
Campeau, P.
;
Lenk, G.
;
Lu, J.
;
Bae, Y.
;
Burrage, L.
;
Turnpenny, P.
;
Corona-Rivera, J.
;
Morandi, L.
;
Mora, M.
;
Reutter, H.
;
Vulto-van Silfhout, A.
;
Faivre, L.
;
Haan, E.
;
Gibbs, R.
;
Meisler, M.
;
Lee, B.
2013
Phosphorylation of serine 779 in fibroblast growth factor receptor 1 and 2 by protein Kinase C(epsilon) regulates Ras/mitogen-activated protein kinase signaling and neuronal differentiation
Lonic, A.
;
Powell, J.
;
Kong, Y.
;
Thomas, D.
;
Holien, J.
;
Truong, N.
;
Parker, M.
;
Guthridge, M.
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.
2013
Tmprss3 loss of function impairs cochlear inner hair cell Kcnma1 channel membrane expression
Molina, L.
;
Fasquelle, L.
;
Nouvian, R.
;
Salvetat, N.
;
Scott, H.
;
Guipponi, M.
;
Molina, F.
;
Puel, J.
;
Delprat, B.
2013
Mechanistic insight into the pathology of polyalanine expansion disorders revealed by a mouse model for x linked hypopituitarism
Hughes, J.
;
Piltz, S.
;
Rogers, N.
;
McAninch, D.
;
Rowley, L.
;
Thomas, P.
;
Camper, S.
2013
Mammalian sex determination and gonad development
Wilhelm, D.
;
Yang, J.
;
Thomas, P.
2013
Impact of dynasore an inhibitor of dynamin II on Shigella flexneri infection
Lum, M.
;
Attridge, S.
;
Morona, R.
;
Mantis, N.J.
Discover
Author
2
Hughes, J.
2
Thomas, P.
1
Attridge, S.
1
Bae, Y.
1
Bellows, S.
1
Burrage, L.
1
Callenbach, P.
1
Campeau, P.
1
Camper, S.
1
Chintawar, S.
.
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Subject
3
Male
2
Disease Models, Animal
2
Exome
2
Female
2
Fluorescent Antibody Technique
2
Genetic Predisposition to Disease
2
Genotype
2
Mutation, Missense
2
Neurons
1
Adolescent
.
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