De Strooper B - Search Results

1

Mitochondria dysfunction and neurodegenerative disorders: cause or consequence.

Morais VA, De Strooper B. Morais VA, et al. Among authors: de strooper b. J Alzheimers Dis. 2010;20 Suppl 2:S255-63. doi: 10.3233/JAD-2010-100345. J Alzheimers Dis. 2010. PMID: 20463408 Review.

2

Gene therapeutic strategies for neurodegenerative diseases.

Baekelandt V, De Strooper B, Nuttin B, Debyser Z. Baekelandt V, et al. Among authors: de strooper b. Curr Opin Mol Ther. 2000 Oct;2(5):540-54. Curr Opin Mol Ther. 2000. PMID: 11249757 Review.

3

A cell biological perspective on mitochondrial dysfunction in Parkinson disease and other neurodegenerative diseases.

Mandemakers W, Morais VA, De Strooper B. Mandemakers W, et al. Among authors: de strooper b. J Cell Sci. 2007 May 15;120(Pt 10):1707-16. doi: 10.1242/jcs.03443. J Cell Sci. 2007. PMID: 17502481 Free article. Review.

4

Alterations of the microRNA network cause neurodegenerative disease.

Hébert SS, De Strooper B. Hébert SS, et al. Among authors: de strooper b. Trends Neurosci. 2009 Apr;32(4):199-206. doi: 10.1016/j.tins.2008.12.003. Epub 2009 Mar 4. Trends Neurosci. 2009. PMID: 19268374 Review.

5

G protein-coupled receptors, cholinergic dysfunction, and Abeta toxicity in Alzheimer's disease.

Thathiah A, De Strooper B. Thathiah A, et al. Among authors: de strooper b. Sci Signal. 2009 Oct 20;2(93):re8. doi: 10.1126/scisignal.293re8. Sci Signal. 2009. PMID: 19843960 Review.

6

Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function.

Morais VA, Verstreken P, Roethig A, Smet J, Snellinx A, Vanbrabant M, Haddad D, Frezza C, Mandemakers W, Vogt-Weisenhorn D, Van Coster R, Wurst W, Scorrano L, De Strooper B. Morais VA, et al. Among authors: de strooper b. EMBO Mol Med. 2009 May;1(2):99-111. doi: 10.1002/emmm.200900006. EMBO Mol Med. 2009. PMID: 20049710 Free PMC article.

7

Dysregulated microRNAs in neurodegenerative disorders.

Lau P, de Strooper B. Lau P, et al. Among authors: de strooper b. Semin Cell Dev Biol. 2010 Sep;21(7):768-73. doi: 10.1016/j.semcdb.2010.01.009. Epub 2010 Jan 18. Semin Cell Dev Biol. 2010. PMID: 20080199 Review.

8

Proteases and proteolysis in Alzheimer disease: a multifactorial view on the disease process.

De Strooper B. De Strooper B. Physiol Rev. 2010 Apr;90(2):465-94. doi: 10.1152/physrev.00023.2009. Physiol Rev. 2010. PMID: 20393191 Free article. Review.

9

The yeast complex I equivalent NADH dehydrogenase rescues pink1 mutants.

Vilain S, Esposito G, Haddad D, Schaap O, Dobreva MP, Vos M, Van Meensel S, Morais VA, De Strooper B, Verstreken P. Vilain S, et al. Among authors: de strooper b. PLoS Genet. 2012 Jan;8(1):e1002456. doi: 10.1371/journal.pgen.1002456. Epub 2012 Jan 5. PLoS Genet. 2012. PMID: 22242018 Free PMC article.

10

Vitamin K2 is a mitochondrial electron carrier that rescues pink1 deficiency.

Vos M, Esposito G, Edirisinghe JN, Vilain S, Haddad DM, Slabbaert JR, Van Meensel S, Schaap O, De Strooper B, Meganathan R, Morais VA, Verstreken P. Vos M, et al. Among authors: de strooper b. Science. 2012 Jun 8;336(6086):1306-10. doi: 10.1126/science.1218632. Epub 2012 May 10. Science. 2012. PMID: 22582012 Free article.

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