Goldman JE - Search Results

1

Metabolic Enzyme Alterations and Astrocyte Dysfunction in a Murine Model of Alexander Disease With Severe Reactive Gliosis.

Heaven MR, Herren AW, Flint DL, Pacheco NL, Li J, Tang A, Khan F, Goldman JE, Phinney BS, Olsen ML. Heaven MR, et al. Among authors: goldman je. Mol Cell Proteomics. 2022 Jan;21(1):100180. doi: 10.1016/j.mcpro.2021.100180. Epub 2021 Nov 20. Mol Cell Proteomics. 2022. PMID: 34808356 Free PMC article.

2

GFAP mutations in Alexander disease.

Li R, Messing A, Goldman JE, Brenner M. Li R, et al. Among authors: goldman je. Int J Dev Neurosci. 2002 Jun-Aug;20(3-5):259-68. doi: 10.1016/s0736-5748(02)00019-9. Int J Dev Neurosci. 2002. PMID: 12175861 Review.

3

Alexander-disease mutation of GFAP causes filament disorganization and decreased solubility of GFAP.

Hsiao VC, Tian R, Long H, Der Perng M, Brenner M, Quinlan RA, Goldman JE. Hsiao VC, et al. Among authors: goldman je. J Cell Sci. 2005 May 1;118(Pt 9):2057-65. doi: 10.1242/jcs.02339. Epub 2005 Apr 19. J Cell Sci. 2005. PMID: 15840648

4

Plectin regulates the organization of glial fibrillary acidic protein in Alexander disease.

Tian R, Gregor M, Wiche G, Goldman JE. Tian R, et al. Among authors: goldman je. Am J Pathol. 2006 Mar;168(3):888-97. doi: 10.2353/ajpath.2006.051028. Am J Pathol. 2006. PMID: 16507904 Free PMC article.

5

Adaptive autophagy in Alexander disease-affected astrocytes.

Tang G, Yue Z, Talloczy Z, Goldman JE. Tang G, et al. Among authors: goldman je. Autophagy. 2008 Jul;4(5):701-3. Epub 2008 Apr 3. Autophagy. 2008. PMID: 18414043 Review.

6

Oligomers of mutant glial fibrillary acidic protein (GFAP) Inhibit the proteasome system in alexander disease astrocytes, and the small heat shock protein alphaB-crystallin reverses the inhibition.

Tang G, Perng MD, Wilk S, Quinlan R, Goldman JE. Tang G, et al. Among authors: goldman je. J Biol Chem. 2010 Apr 2;285(14):10527-37. doi: 10.1074/jbc.M109.067975. Epub 2010 Jan 28. J Biol Chem. 2010. PMID: 20110364 Free PMC article.

7

Alexander disease mutant glial fibrillary acidic protein compromises glutamate transport in astrocytes.

Tian R, Wu X, Hagemann TL, Sosunov AA, Messing A, McKhann GM, Goldman JE. Tian R, et al. Among authors: goldman je. J Neuropathol Exp Neurol. 2010 Apr;69(4):335-45. doi: 10.1097/NEN.0b013e3181d3cb52. J Neuropathol Exp Neurol. 2010. PMID: 20448479 Free PMC article.

8

Splice site, frameshift, and chimeric GFAP mutations in Alexander disease.

Flint D, Li R, Webster LS, Naidu S, Kolodny E, Percy A, van der Knaap M, Powers JM, Mantovani JF, Ekstein J, Goldman JE, Messing A, Brenner M. Flint D, et al. Among authors: goldman je. Hum Mutat. 2012 Jul;33(7):1141-8. doi: 10.1002/humu.22094. Epub 2012 Apr 30. Hum Mutat. 2012. PMID: 22488673 Free PMC article.

9

Phenotypic conversions of "protoplasmic" to "reactive" astrocytes in Alexander disease.

Sosunov AA, Guilfoyle E, Wu X, McKhann GM 2nd, Goldman JE. Sosunov AA, et al. Among authors: goldman je. J Neurosci. 2013 Apr 24;33(17):7439-50. doi: 10.1523/JNEUROSCI.4506-12.2013. J Neurosci. 2013. PMID: 23616550 Free PMC article.

10

Astrocytic TDP-43 pathology in Alexander disease.

Walker AK, Daniels CM, Goldman JE, Trojanowski JQ, Lee VM, Messing A. Walker AK, et al. Among authors: goldman je. J Neurosci. 2014 May 7;34(19):6448-58. doi: 10.1523/JNEUROSCI.0248-14.2014. J Neurosci. 2014. PMID: 24806671 Free PMC article.

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