Meitinger T - Search Results

1

Cellular rescue-assay aids verification of causative DNA-variants in mitochondrial complex I deficiency.

Danhauser K, Iuso A, Haack TB, Freisinger P, Brockmann K, Mayr JA, Meitinger T, Prokisch H. Danhauser K, et al. Among authors: meitinger t. Mol Genet Metab. 2011 Jun;103(2):161-6. doi: 10.1016/j.ymgme.2011.03.004. Epub 2011 Mar 11. Mol Genet Metab. 2011. PMID: 21458341

2

An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria.

Hörtnagel K, Prokisch H, Meitinger T. Hörtnagel K, et al. Among authors: meitinger t. Hum Mol Genet. 2003 Feb 1;12(3):321-7. doi: 10.1093/hmg/ddg026. Hum Mol Genet. 2003. PMID: 12554685

3

Integrative analysis of the mitochondrial proteome in yeast.

Prokisch H, Scharfe C, Camp DG 2nd, Xiao W, David L, Andreoli C, Monroe ME, Moore RJ, Gritsenko MA, Kozany C, Hixson KK, Mottaz HM, Zischka H, Ueffing M, Herman ZS, Davis RW, Meitinger T, Oefner PJ, Smith RD, Steinmetz LM. Prokisch H, et al. Among authors: meitinger t. PLoS Biol. 2004 Jun;2(6):e160. doi: 10.1371/journal.pbio.0020160. Epub 2004 Jun 15. PLoS Biol. 2004. PMID: 15208715 Free PMC article.

4

Mechanisms for multiple intracellular localization of human mitochondrial proteins.

Mueller JC, Andreoli C, Prokisch H, Meitinger T. Mueller JC, et al. Among authors: meitinger t. Mitochondrion. 2004 May;3(6):315-25. doi: 10.1016/j.mito.2004.02.002. Mitochondrion. 2004. PMID: 16120363

5

Proteome analysis of mitochondrial outer membrane from Neurospora crassa.

Schmitt S, Prokisch H, Schlunck T, Camp DG 2nd, Ahting U, Waizenegger T, Scharfe C, Meitinger T, Imhof A, Neupert W, Oefner PJ, Rapaport D. Schmitt S, et al. Among authors: meitinger t. Proteomics. 2006 Jan;6(1):72-80. doi: 10.1002/pmic.200402084. Proteomics. 2006. PMID: 16294304

6

The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity.

Gloeckner CJ, Kinkl N, Schumacher A, Braun RJ, O'Neill E, Meitinger T, Kolch W, Prokisch H, Ueffing M. Gloeckner CJ, et al. Among authors: meitinger t. Hum Mol Genet. 2006 Jan 15;15(2):223-32. doi: 10.1093/hmg/ddi439. Epub 2005 Dec 1. Hum Mol Genet. 2006. PMID: 16321986

7

Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation.

Hartig MB, Hörtnagel K, Garavaglia B, Zorzi G, Kmiec T, Klopstock T, Rostasy K, Svetel M, Kostic VS, Schuelke M, Botz E, Weindl A, Novakovic I, Nardocci N, Prokisch H, Meitinger T. Hartig MB, et al. Among authors: meitinger t. Ann Neurol. 2006 Feb;59(2):248-56. doi: 10.1002/ana.20771. Ann Neurol. 2006. PMID: 16437574

8

A population-based epidemiological and genetic study of X-linked retinitis pigmentosa.

Prokisch H, Hartig M, Hellinger R, Meitinger T, Rosenberg T. Prokisch H, et al. Among authors: meitinger t. Invest Ophthalmol Vis Sci. 2007 Sep;48(9):4012-8. doi: 10.1167/iovs.07-0071. Invest Ophthalmol Vis Sci. 2007. PMID: 17724181

9

SLC2A9 influences uric acid concentrations with pronounced sex-specific effects.

Döring A, Gieger C, Mehta D, Gohlke H, Prokisch H, Coassin S, Fischer G, Henke K, Klopp N, Kronenberg F, Paulweber B, Pfeufer A, Rosskopf D, Völzke H, Illig T, Meitinger T, Wichmann HE, Meisinger C. Döring A, et al. Among authors: meitinger t. Nat Genet. 2008 Apr;40(4):430-6. doi: 10.1038/ng.107. Epub 2008 Mar 9. Nat Genet. 2008. PMID: 18327256

10

MitoP2: an integrative tool for the analysis of the mitochondrial proteome.

Elstner M, Andreoli C, Ahting U, Tetko I, Klopstock T, Meitinger T, Prokisch H. Elstner M, et al. Among authors: meitinger t. Mol Biotechnol. 2008 Nov;40(3):306-15. doi: 10.1007/s12033-008-9100-5. Epub 2008 Sep 9. Mol Biotechnol. 2008. PMID: 18780189 Review.

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