Olsen ML - Search Results

1

Microbial community changes in a female rat model of Rett syndrome.

Gallucci A, Patterson KC, Weit AR, Van Der Pol WJ, Dubois LG, Percy AK, Morrow CD, Campbell SL, Olsen ML. Gallucci A, et al. Among authors: olsen ml. Prog Neuropsychopharmacol Biol Psychiatry. 2021 Jul 13;109:110259. doi: 10.1016/j.pnpbp.2021.110259. Epub 2021 Feb 4. Prog Neuropsychopharmacol Biol Psychiatry. 2021. PMID: 33548354 Free PMC article.

2

Functional expression of Kir4.1 channels in spinal cord astrocytes.

Olsen ML, Higashimori H, Campbell SL, Hablitz JJ, Sontheimer H. Olsen ML, et al. Glia. 2006 Apr 1;53(5):516-28. doi: 10.1002/glia.20312. Glia. 2006. PMID: 16369934 Free PMC article.

3

Differential distribution of Kir4.1 in spinal cord astrocytes suggests regional differences in K+ homeostasis.

Olsen ML, Campbell SL, Sontheimer H. Olsen ML, et al. J Neurophysiol. 2007 Aug;98(2):786-93. doi: 10.1152/jn.00340.2007. Epub 2007 Jun 20. J Neurophysiol. 2007. PMID: 17581847 Free PMC article.

4

Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.

Cuddapah VA, Pillai RB, Shekar KV, Lane JB, Motil KJ, Skinner SA, Tarquinio DC, Glaze DG, McGwin G, Kaufmann WE, Percy AK, Neul JL, Olsen ML. Cuddapah VA, et al. Among authors: olsen ml. J Med Genet. 2014 Mar;51(3):152-8. doi: 10.1136/jmedgenet-2013-102113. Epub 2014 Jan 7. J Med Genet. 2014. PMID: 24399845 Free PMC article.

5

Functional changes in glutamate transporters and astrocyte biophysical properties in a rodent model of focal cortical dysplasia.

Campbell SL, Hablitz JJ, Olsen ML. Campbell SL, et al. Among authors: olsen ml. Front Cell Neurosci. 2014 Dec 17;8:425. doi: 10.3389/fncel.2014.00425. eCollection 2014. Front Cell Neurosci. 2014. PMID: 25565960 Free PMC article.

6

The role of glial-specific Kir4.1 in normal and pathological states of the CNS.

Nwaobi SE, Cuddapah VA, Patterson KC, Randolph AC, Olsen ML. Nwaobi SE, et al. Among authors: olsen ml. Acta Neuropathol. 2016 Jul;132(1):1-21. doi: 10.1007/s00401-016-1553-1. Epub 2016 Mar 9. Acta Neuropathol. 2016. PMID: 26961251 Free PMC article. Review.

7

MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats.

Patterson KC, Hawkins VE, Arps KM, Mulkey DK, Olsen ML. Patterson KC, et al. Among authors: olsen ml. Hum Mol Genet. 2016 Aug 1;25(15):3303-3320. doi: 10.1093/hmg/ddw179. Epub 2016 Jun 21. Hum Mol Genet. 2016. PMID: 27329765 Free PMC article.

8

MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats.

Patterson KC, Hawkins VE, Arps KM, Mulkey DK, Olsen ML. Patterson KC, et al. Among authors: olsen ml. Hum Mol Genet. 2016 Dec 15;25(24):5514-5515. doi: 10.1093/hmg/ddw435. Hum Mol Genet. 2016. PMID: 28201743 Free PMC article. No abstract available.

9

RNA sequencing and proteomics approaches reveal novel deficits in the cortex of Mecp2-deficient mice, a model for Rett syndrome.

Pacheco NL, Heaven MR, Holt LM, Crossman DK, Boggio KJ, Shaffer SA, Flint DL, Olsen ML. Pacheco NL, et al. Among authors: olsen ml. Mol Autism. 2017 Oct 24;8:56. doi: 10.1186/s13229-017-0174-4. eCollection 2017. Mol Autism. 2017. PMID: 29090078 Free PMC article.

10

MeCP2 Deficiency Leads to Loss of Glial Kir4.1.

Kahanovitch U, Cuddapah VA, Pacheco NL, Holt LM, Mulkey DK, Percy AK, Olsen ML. Kahanovitch U, et al. Among authors: olsen ml. eNeuro. 2018 Feb 19;5(1):ENEURO.0194-17.2018. doi: 10.1523/ENEURO.0194-17.2018. eCollection 2018 Jan-Feb. eNeuro. 2018. PMID: 29464197 Free PMC article.

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