Mayer-Pröschel M - Search Results

1

A novel mouse model for ataxia-telangiectasia with a N-terminal mutation displays a behavioral defect and a low incidence of lymphoma but no increased oxidative burden.

Campbell A, Krupp B, Bushman J, Noble M, Pröschel C, Mayer-Pröschel M. Campbell A, et al. Hum Mol Genet. 2015 Nov 15;24(22):6331-49. doi: 10.1093/hmg/ddv342. Epub 2015 Aug 26. Hum Mol Genet. 2015. PMID: 26310626 Free PMC article.

2

Mutation of ataxia-telangiectasia mutated is associated with dysfunctional glutathione homeostasis in cerebellar astroglia.

Campbell A, Bushman J, Munger J, Noble M, Pröschel C, Mayer-Pröschel M. Campbell A, et al. Glia. 2016 Feb;64(2):227-39. doi: 10.1002/glia.22925. Epub 2015 Oct 15. Glia. 2016. PMID: 26469940 Free PMC article.

3

Redox regulation of precursor cell function: insights and paradoxes.

Noble M, Mayer-Pröschel M, Pröschel C. Noble M, et al. Antioxid Redox Signal. 2005 Nov-Dec;7(11-12):1456-67. doi: 10.1089/ars.2005.7.1456. Antioxid Redox Signal. 2005. PMID: 16356108 Review.

4

Heterozygote galactocerebrosidase (GALC) mutants have reduced remyelination and impaired myelin debris clearance following demyelinating injury.

Scott-Hewitt NJ, Folts CJ, Hogestyn JM, Piester G, Mayer-Pröschel M, Noble MD. Scott-Hewitt NJ, et al. Among authors: mayer proschel m. Hum Mol Genet. 2017 Aug 1;26(15):2825-2837. doi: 10.1093/hmg/ddx153. Hum Mol Genet. 2017. PMID: 28575206 Free PMC article.

5

Ataxia-telangiectasia mutated is required for the development of protective immune memory after influenza A virus infection.

Warren R, Domm W, Yee M, Campbell A, Malone J, Wright T, Mayer-Pröschel M, O'Reilly MA. Warren R, et al. Among authors: mayer proschel m. Am J Physiol Lung Cell Mol Physiol. 2019 Nov 1;317(5):L591-L601. doi: 10.1152/ajplung.00031.2019. Epub 2019 Sep 11. Am J Physiol Lung Cell Mol Physiol. 2019. PMID: 31509427 Free PMC article.

6

Redox state as a central modulator of precursor cell function.

Noble M, Smith J, Power J, Mayer-Pröschel M. Noble M, et al. Ann N Y Acad Sci. 2003 Jun;991:251-71. doi: 10.1111/j.1749-6632.2003.tb07481.x. Ann N Y Acad Sci. 2003. PMID: 12846992 Review.

7

EIF2B5 mutations compromise GFAP+ astrocyte generation in vanishing white matter leukodystrophy.

Dietrich J, Lacagnina M, Gass D, Richfield E, Mayer-Pröschel M, Noble M, Torres C, Pröschel C. Dietrich J, et al. Nat Med. 2005 Mar;11(3):277-83. doi: 10.1038/nm1195. Epub 2005 Feb 20. Nat Med. 2005. PMID: 15723074

8

Precursor cell biology and the development of astrocyte transplantation therapies: lessons from spinal cord injury.

Noble M, Davies JE, Mayer-Pröschel M, Pröschel C, Davies SJ. Noble M, et al. Neurotherapeutics. 2011 Oct;8(4):677-93. doi: 10.1007/s13311-011-0071-z. Neurotherapeutics. 2011. PMID: 21918888 Free PMC article. Review.

9

iOPs: a new tool for studying myelin pathologies?

Noble M, Mayer-Pröschel M, Pröschel C. Noble M, et al. Cell Stem Cell. 2013 May 2;12(5):503-4. doi: 10.1016/j.stem.2013.04.021. Cell Stem Cell. 2013. PMID: 23642358 Free article.

10

Oligodendrocyte/type-2 astrocyte progenitor cells and glial-restricted precursor cells generate different tumor phenotypes in response to the identical oncogenes.

Wang J, Bushman J, Wang X, Mayer-Proschel M, Johnson M, Noble M. Wang J, et al. J Neurosci. 2013 Oct 16;33(42):16805-17. doi: 10.1523/JNEUROSCI.0546-13.2013. J Neurosci. 2013. PMID: 24133281 Free PMC article.

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