Schüle B - Search Results

1

Loss-of-Function NUBPL Mutation May Link Parkinson's Disease to Recessive Complex I Deficiency.

Eis PS, Huang N, Langston JW, Hatchwell E, Schüle B. Eis PS, et al. Among authors: schule b. Front Neurol. 2020 Oct 29;11:555961. doi: 10.3389/fneur.2020.555961. eCollection 2020. Front Neurol. 2020. PMID: 33224084 Free PMC article.

2

Novel features in a patient homozygous for the L347P mutation in the PINK1 gene.

Doostzadeh J, Tetrud JW, Allen-Auerbach M, Langston JW, Schüle B. Doostzadeh J, et al. Among authors: schule b. Parkinsonism Relat Disord. 2007 Aug;13(6):359-61. doi: 10.1016/j.parkreldis.2006.08.009. Epub 2006 Oct 19. Parkinsonism Relat Disord. 2007. PMID: 17055324

3

Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.

Fuchs J, Nilsson C, Kachergus J, Munz M, Larsson EM, Schüle B, Langston JW, Middleton FA, Ross OA, Hulihan M, Gasser T, Farrer MJ. Fuchs J, et al. Among authors: schule b. Neurology. 2007 Mar 20;68(12):916-22. doi: 10.1212/01.wnl.0000254458.17630.c5. Epub 2007 Jan 24. Neurology. 2007. PMID: 17251522

4

Parkin gene variations and parkinsonism: association does not imply causation.

Langston JW, Tanner CM, Schüle B. Langston JW, et al. Among authors: schule b. Ann Neurol. 2007 Jan;61(1):4-6. doi: 10.1002/ana.21069. Ann Neurol. 2007. PMID: 17262853 No abstract available.

5

Alpha-synuclein-glucocerebrosidase interactions in pharmacological Gaucher models: a biological link between Gaucher disease and parkinsonism.

Manning-Boğ AB, Schüle B, Langston JW. Manning-Boğ AB, et al. Among authors: schule b. Neurotoxicology. 2009 Nov;30(6):1127-32. doi: 10.1016/j.neuro.2009.06.009. Epub 2009 Jul 2. Neurotoxicology. 2009. PMID: 19576930

6

Can cellular models revolutionize drug discovery in Parkinson's disease?

Schüle B, Pera RA, Langston JW. Schüle B, et al. Biochim Biophys Acta. 2009 Nov;1792(11):1043-51. doi: 10.1016/j.bbadis.2009.08.014. Epub 2009 Sep 3. Biochim Biophys Acta. 2009. PMID: 19733239 Free article. Review.

7

Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers.

Marras C, Schüle B, Munhoz RP, Rogaeva E, Langston JW, Kasten M, Meaney C, Klein C, Wadia PM, Lim SY, Chuang RS, Zadikof C, Steeves T, Prakash KM, de Bie RM, Adeli G, Thomsen T, Johansen KK, Teive HA, Asante A, Reginold W, Lang AE. Marras C, et al. Among authors: schule b. Neurology. 2011 Jul 26;77(4):325-33. doi: 10.1212/WNL.0b013e318227042d. Epub 2011 Jul 13. Neurology. 2011. PMID: 21753163 Free PMC article.

8

SNCA triplication Parkinson's patient's iPSC-derived DA neurons accumulate α-synuclein and are susceptible to oxidative stress.

Byers B, Cord B, Nguyen HN, Schüle B, Fenno L, Lee PC, Deisseroth K, Langston JW, Pera RR, Palmer TD. Byers B, et al. Among authors: schule b. PLoS One. 2011;6(11):e26159. doi: 10.1371/journal.pone.0026159. Epub 2011 Nov 16. PLoS One. 2011. PMID: 22110584 Free PMC article.

9

Small molecules greatly improve conversion of human-induced pluripotent stem cells to the neuronal lineage.

Mak SK, Huang YA, Iranmanesh S, Vangipuram M, Sundararajan R, Nguyen L, Langston JW, Schüle B. Mak SK, et al. Among authors: schule b. Stem Cells Int. 2012;2012:140427. doi: 10.1155/2012/140427. Epub 2012 Apr 10. Stem Cells Int. 2012. PMID: 22567022 Free PMC article.

10

Mitochondrial dysfunction in skin fibroblasts from a Parkinson's disease patient with an alpha-synuclein triplication.

Mak SK, Tewari D, Tetrud JW, Langston JW, Schüle B. Mak SK, et al. Among authors: schule b. J Parkinsons Dis. 2011;1(2):175-83. doi: 10.3233/JPD-2011-11025. J Parkinsons Dis. 2011. PMID: 23934919

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