Noebels JL[au] - Search Results

Year	Number of Results
1975	1
1977	2
1978	3
1979	2
1981	1
1984	2
1986	1
1989	1
1990	2
1991	4
1992	2
1993	3
1994	2
1995	4
1996	4
1997	5
1998	6
1999	8
2000	9
2001	7
2002	6
2003	10
2004	5
2005	6
2006	4
2007	6
2008	4
2009	6
2010	5
2011	8
2012	6
2013	9
2014	7
2015	7
2016	9
2017	5
2018	2
2019	4
2020	5
2021	3

1

Identification of diverse astrocyte populations and their malignant analogs.

John Lin CC, Yu K, Hatcher A, Huang TW, Lee HK, Carlson J, Weston MC, Chen F, Zhang Y, Zhu W, Mohila CA, Ahmed N, Patel AJ, Arenkiel BR, Noebels JL, Creighton CJ, Deneen B. John Lin CC, et al. Among authors: noebels jl. Nat Neurosci. 2017 Mar;20(3):396-405. doi: 10.1038/nn.4493. Epub 2017 Feb 6. Nat Neurosci. 2017. PMID: 28166219 Free PMC article.

2

PIK3CA variants selectively initiate brain hyperactivity during gliomagenesis.

Yu K, Lin CJ, Hatcher A, Lozzi B, Kong K, Huang-Hobbs E, Cheng YT, Beechar VB, Zhu W, Zhang Y, Chen F, Mills GB, Mohila CA, Creighton CJ, Noebels JL, Scott KL, Deneen B. Yu K, et al. Among authors: noebels jl. Nature. 2020 Feb;578(7793):166-171. doi: 10.1038/s41586-020-1952-2. Epub 2020 Jan 29. Nature. 2020. PMID: 31996845 Free PMC article.

3

Therapeutic inhibition of mTORC2 rescues the behavioral and neurophysiological abnormalities associated with Pten-deficiency.

Chen CJ, Sgritta M, Mays J, Zhou H, Lucero R, Park J, Wang IC, Park JH, Kaipparettu BA, Stoica L, Jafar-Nejad P, Rigo F, Chin J, Noebels JL, Costa-Mattioli M. Chen CJ, et al. Among authors: noebels jl. Nat Med. 2019 Nov;25(11):1684-1690. doi: 10.1038/s41591-019-0608-y. Epub 2019 Oct 21. Nat Med. 2019. PMID: 31636454 Free PMC article.

4

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.

Chao HT, Chen H, Samaco RC, Xue M, Chahrour M, Yoo J, Neul JL, Gong S, Lu HC, Heintz N, Ekker M, Rubenstein JL, Noebels JL, Rosenmund C, Zoghbi HY. Chao HT, et al. Among authors: noebels jl. Nature. 2010 Nov 11;468(7321):263-9. doi: 10.1038/nature09582. Nature. 2010. PMID: 21068835 Free PMC article.

5

Pathogenesis of peritumoral hyperexcitability in an immunocompetent CRISPR-based glioblastoma model.

Hatcher A, Yu K, Meyer J, Aiba I, Deneen B, Noebels JL. Hatcher A, et al. Among authors: noebels jl. J Clin Invest. 2020 May 1;130(5):2286-2300. doi: 10.1172/JCI133316. J Clin Invest. 2020. PMID: 32250339 Free PMC article.

6

Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein.

Tang M, Gao G, Rueda CB, Yu H, Thibodeaux DN, Awano T, Engelstad KM, Sanchez-Quintero MJ, Yang H, Li F, Li H, Su Q, Shetler KE, Jones L, Seo R, McConathy J, Hillman EM, Noebels JL, De Vivo DC, Monani UR. Tang M, et al. Among authors: noebels jl. Nat Commun. 2017 Jan 20;8:14152. doi: 10.1038/ncomms14152. Nat Commun. 2017. PMID: 28106060 Free PMC article.

7

Aberrant excitatory neuronal activity and compensatory remodeling of inhibitory hippocampal circuits in mouse models of Alzheimer's disease.

Palop JJ, Chin J, Roberson ED, Wang J, Thwin MT, Bien-Ly N, Yoo J, Ho KO, Yu GQ, Kreitzer A, Finkbeiner S, Noebels JL, Mucke L. Palop JJ, et al. Among authors: noebels jl. Neuron. 2007 Sep 6;55(5):697-711. doi: 10.1016/j.neuron.2007.07.025. Neuron. 2007. PMID: 17785178 Free PMC article.

8

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

Collins AL, Levenson JM, Vilaythong AP, Richman R, Armstrong DL, Noebels JL, David Sweatt J, Zoghbi HY. Collins AL, et al. Among authors: noebels jl. Hum Mol Genet. 2004 Nov 1;13(21):2679-89. doi: 10.1093/hmg/ddh282. Epub 2004 Sep 6. Hum Mol Genet. 2004. PMID: 15351775

9

Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation.

Jiang YH, Armstrong D, Albrecht U, Atkins CM, Noebels JL, Eichele G, Sweatt JD, Beaudet AL. Jiang YH, et al. Among authors: noebels jl. Neuron. 1998 Oct;21(4):799-811. doi: 10.1016/s0896-6273(00)80596-6. Neuron. 1998. PMID: 9808466 Free article.

10

Predicting the impact of sodium channel mutations in human brain disease.

Noebels JL. Noebels JL. Epilepsia. 2019 Dec;60 Suppl 3(Suppl 3):S8-S16. doi: 10.1111/epi.14724. Epilepsia. 2019. PMID: 31904123 Free PMC article. Review.

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