Faust PL - Search Results

1

Reduced Bergmann glial process terminations and lateral appendages in essential tremor.

Ruff DS, Balbo I, Lai RY, Dieng D, Hennessey C, Vennam K, Dwork AJ, McCreary M, Louis ED, Faust PL, Kuo SH. Ruff DS, et al. Among authors: faust pl. Ann Clin Transl Neurol. 2024 Feb;11(2):377-388. doi: 10.1002/acn3.51958. Epub 2023 Dec 14. Ann Clin Transl Neurol. 2024. PMID: 38098226 Free PMC article.

2

Peroxisome deficiency causes a complex phenotype because of hepatic SREBP/Insig dysregulation associated with endoplasmic reticulum stress.

Kovacs WJ, Tape KN, Shackelford JE, Wikander TM, Richards MJ, Fliesler SJ, Krisans SK, Faust PL. Kovacs WJ, et al. Among authors: faust pl. J Biol Chem. 2009 Mar 13;284(11):7232-45. doi: 10.1074/jbc.M809064200. Epub 2008 Dec 24. J Biol Chem. 2009. PMID: 19110480 Free PMC article.

3

Neuropathology of lubag (x-linked dystonia parkinsonism).

Waters CH, Faust PL, Powers J, Vinters H, Moskowitz C, Nygaard T, Hunt AL, Fahn S. Waters CH, et al. Among authors: faust pl. Mov Disord. 1993 Jul;8(3):387-90. doi: 10.1002/mds.870080328. Mov Disord. 1993. PMID: 8341310

4

New directions for neuronal migration.

Pearlman AL, Faust PL, Hatten ME, Brunstrom JE. Pearlman AL, et al. Among authors: faust pl. Curr Opin Neurobiol. 1998 Feb;8(1):45-54. doi: 10.1016/s0959-4388(98)80007-x. Curr Opin Neurobiol. 1998. PMID: 9568391 Free article. Review.

5

Purification of brain peroxisomes and localization of 3-hydroxy-3-methylglutaryl coenzyme A reductase.

Kovacs WJ, Faust PL, Keller GA, Krisans SK. Kovacs WJ, et al. Among authors: faust pl. Eur J Biochem. 2001 Sep;268(18):4850-9. doi: 10.1046/j.0014-2956.2001.02409.x. Eur J Biochem. 2001. PMID: 11559353 Free article.

6

Phenotypic variability of CADASIL and novel morphologic findings.

Rubio A, Rifkin D, Powers JM, Patel U, Stewart J, Faust P, Goldman JE, Mohr JP, Numaguchi Y, Jensen K. Rubio A, et al. Acta Neuropathol. 1997 Sep;94(3):247-54. doi: 10.1007/s004010050700. Acta Neuropathol. 1997. PMID: 9292694

7

Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.

Faust PL, Hatten ME. Faust PL, et al. J Cell Biol. 1997 Dec 1;139(5):1293-305. doi: 10.1083/jcb.139.5.1293. J Cell Biol. 1997. PMID: 9382874 Free PMC article.

8

Expression of human cathepsin D in Xenopus oocytes: phosphorylation and intracellular targeting.

Faust PL, Wall DA, Perara E, Lingappa VR, Kornfeld S. Faust PL, et al. J Cell Biol. 1987 Nov;105(5):1937-45. doi: 10.1083/jcb.105.5.1937. J Cell Biol. 1987. PMID: 3680368 Free PMC article.

9

Renin, a secretory glycoprotein, acquires phosphomannosyl residues.

Faust PL, Chirgwin JM, Kornfeld S. Faust PL, et al. J Cell Biol. 1987 Nov;105(5):1947-55. doi: 10.1083/jcb.105.5.1947. J Cell Biol. 1987. PMID: 2960682 Free PMC article.

10

alpha-Synuclein abnormalities in mouse models of peroxisome biogenesis disorders.

Yakunin E, Moser A, Loeb V, Saada A, Faust P, Crane DI, Baes M, Sharon R. Yakunin E, et al. J Neurosci Res. 2010 Mar;88(4):866-76. doi: 10.1002/jnr.22246. J Neurosci Res. 2010. PMID: 19830841 Free PMC article.

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