Lücking CB - Search Results

1

Complex relationship between Parkin mutations and Parkinson disease.

West A, Periquet M, Lincoln S, Lücking CB, Nicholl D, Bonifati V, Rawal N, Gasser T, Lohmann E, Deleuze JF, Maraganore D, Levey A, Wood N, Dürr A, Hardy J, Brice A, Farrer M; French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility on Parkinson's Disease. West A, et al. Among authors: lucking cb. Am J Med Genet. 2002 Jul 8;114(5):584-91. doi: 10.1002/ajmg.10525. Am J Med Genet. 2002. PMID: 12116199

2

Semiquantitative PCR for the detection of exon rearrangements in the Parkin gene.

Lücking CB, Brice A. Lücking CB, et al. Methods Mol Biol. 2003;217:13-26. doi: 10.1385/1-59259-330-5:13. Methods Mol Biol. 2003. PMID: 12491917 No abstract available.

3

Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism.

Illarioshkin SN, Periquet M, Rawal N, Lücking CB, Zagorovskaya TB, Slominsky PA, Miloserdova OV, Markova ED, Limborska SA, Ivanova-Smolenskaya IA, Brice A. Illarioshkin SN, et al. Among authors: lucking cb. Mov Disord. 2003 Aug;18(8):914-9. doi: 10.1002/mds.10467. Mov Disord. 2003. PMID: 12889082

4

Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease.

Klopstock T, Elstner M, Lücking CB, Müller-Myhsok B, Gasser T, Botz E, Lichtner P, Hörtnagel K. Klopstock T, et al. Among authors: lucking cb. Neurosci Lett. 2005 May 13;379(3):195-8. doi: 10.1016/j.neulet.2004.12.061. Neurosci Lett. 2005. PMID: 15843062

5

Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death.

Darios F, Corti O, Lücking CB, Hampe C, Muriel MP, Abbas N, Gu WJ, Hirsch EC, Rooney T, Ruberg M, Brice A. Darios F, et al. Among authors: lucking cb. Hum Mol Genet. 2003 Mar 1;12(5):517-26. doi: 10.1093/hmg/ddg044. Hum Mol Genet. 2003. PMID: 12588799

6

The C289G and C418R missense mutations cause rapid sequestration of human Parkin into insoluble aggregates.

Gu WJ, Corti O, Araujo F, Hampe C, Jacquier S, Lücking CB, Abbas N, Duyckaerts C, Rooney T, Pradier L, Ruberg M, Brice A. Gu WJ, et al. Among authors: lucking cb. Neurobiol Dis. 2003 Dec;14(3):357-64. doi: 10.1016/j.nbd.2003.08.011. Neurobiol Dis. 2003. PMID: 14678753

7

Proteasomal inhibition reduces parkin mRNA in PC12 and SH-SY5Y cells.

Koch A, Lehmann-Horn K, Dächsel JC, Gasser T, Kahle PJ, Lücking CB. Koch A, et al. Among authors: lucking cb. Parkinsonism Relat Disord. 2009 Mar;15(3):220-5. doi: 10.1016/j.parkreldis.2008.05.005. Epub 2008 Jun 30. Parkinsonism Relat Disord. 2009. PMID: 18586549

8

Nonradioactive PCR sequencing using digoxigenin.

Kösel S, Lücking CB, Egensperger R, Graeber MB. Kösel S, et al. Among authors: lucking cb. Methods Mol Biol. 1996;65:81-9. doi: 10.1385/0-89603-344-9:81. Methods Mol Biol. 1996. PMID: 8956254 No abstract available.

9

Nonradioactive PCR sequencing using digoxigenin.

Kösel S, Lücking CB, Egensperger R, Graeber MB. Kösel S, et al. Among authors: lucking cb. Methods Mol Biol. 2003;226:347-54. doi: 10.1385/1-59259-384-4:347. Methods Mol Biol. 2003. PMID: 12958520 No abstract available.

10

Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonism.

Kösel S, Lücking CB, Egensperger R, Mehraein P, Graeber MB. Kösel S, et al. Among authors: lucking cb. J Neurosci Res. 1996 Apr 15;44(2):174-83. doi: 10.1002/(SICI)1097-4547(19960415)44:2<174::AID-JNR10>3.0.CO;2-6. J Neurosci Res. 1996. PMID: 8723226

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