Noebels
Noebels
Professor of Neurology, Baylor College of Medicine
Verified email at bcm.edu
Title
Cited by
Cited by
Year
Aberrant excitatory neuronal activity and compensatory remodeling of inhibitory hippocampal circuits in mouse models of Alzheimer's disease
JJ Palop, J Chin, ED Roberson, J Wang, MT Thwin, N Bien-Ly, J Yoo, ...
Neuron 55 (5), 697-711, 2007
12972007
Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes
HT Chao, H Chen, RC Samaco, M Xue, M Chahrour, J Yoo, JL Neul, ...
Nature 468 (7321), 263-269, 2010
10362010
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
MD Shahbazian, JI Young, LA Yuva-Paylor, CM Spencer, BA Antalffy, ...
Neuron 35 (2), 243-254, 2002
8322002
Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation
Y Jiang, D Armstrong, U Albrecht, CM Atkins, JL Noebels, G Eichele, ...
Neuron 21 (4), 799-811, 1998
8031998
Amyloid-β/Fyn–induced synaptic, network, and cognitive impairments depend on tau levels in multiple mouse models of Alzheimer's disease
ED Roberson, B Halabisky, JW Yoo, J Yao, J Chin, F Yan, T Wu, P Hamto, ...
Journal of Neuroscience 31 (2), 700-711, 2011
6142011
Mild overexpression of MeCP2 causes a progressive neurological disorder in mice
AL Collins, JM Levenson, AP Vilaythong, R Richman, DL Armstrong, ...
Human molecular genetics 13 (21), 2679-2689, 2004
5882004
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
T Matsuura, T Yamagata, DL Burgess, A Rasmussen, RP Grewal, ...
Nature genetics 26 (2), 191-194, 2000
5382000
Mutation of the Ca2+ channel β subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse
DL Burgess, JM Jones, MH Meisler, JL Noebels
Cell 88 (3), 385-392, 1997
5091997
Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy
I Cobos, ME Calcagnotto, AJ Vilaythong, MT Thwin, JL Noebels, ...
Nature neuroscience 8 (8), 1059-1068, 2005
4902005
“Jasper’s Basic Mechanisms of the Epilepsies” Workshop
JL Noebels, M Avoli, M Rogawski, R Olsen, AV Delgado‐Escueta
Epilepsia 51, 1-5, 2010
441*2010
Mutation in AP-3 δ in the mocha mouse links endosomal transport to storage deficiency in platelets, melanosomes, and synaptic vesicles
P Kantheti, X Qiao, ME Diaz, AA Peden, GE Meyer, SL Carskadon, ...
Neuron 21 (1), 111-122, 1998
4391998
Genetic disruption of cortical interneuron development causes region-and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction
EM Powell, DB Campbell, GD Stanwood, C Davis, JL Noebels, P Levitt
Journal of Neuroscience 23 (2), 622-631, 2003
3672003
BK channel β4 subunit reduces dentate gyrus excitability and protects against temporal lobe seizures
R Brenner, QH Chen, A Vilaythong, GM Toney, JL Noebels, RW Aldrich
Nature neuroscience 8 (12), 1752-1759, 2005
3602005
Epilepsy in mice deficient in the 65-kDa isoform of glutamic acid decarboxylase
SF Kash, RS Johnson, LH Tecott, JL Noebels, RD Mayfield, D Hanahan, ...
Proceedings of the National Academy of Sciences 94 (25), 14060-14065, 1997
3581997
Sensorineural deafness and seizures in mice lacking vesicular glutamate transporter 3
RP Seal, O Akil, E Yi, CM Weber, L Grant, J Yoo, A Clause, K Kandler, ...
Neuron 57 (2), 263-275, 2008
3572008
Loss of BETA2/NeuroD leads to malformation of the dentate gyrus and epilepsy
M Liu, SJ Pleasure, AE Collins, JL Noebels, FJ Naya, MJ Tsai, ...
Proceedings of the National Academy of Sciences 97 (2), 865-870, 2000
3302000
Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice
LA Pennacchio, DM Bouley, KM Higgins, MP Scott, JL Noebels, ...
Nature genetics 20 (3), 251-258, 1998
3171998
Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse tottering
JL Noebels, RL Sidman
Science 204 (4399), 1334-1336, 1979
3101979
The biology of epilepsy genes
JL Noebels
Annual review of neuroscience 26 (1), 599-625, 2003
3022003
Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice
GA Cox, CM Lutz, CL Yang, D Biemesderfer, RT Bronson, A Fu, ...
Cell 91 (1), 139-148, 1997
2941997
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Articles 1–20