Meitinger T - Search Results

1

Severe respiratory complex III defect prevents liver adaptation to prolonged fasting.

Kremer LS, L'hermitte-Stead C, Lesimple P, Gilleron M, Filaut S, Jardel C, Haack TB, Strom TM, Meitinger T, Azzouz H, Tebib N, Ogier de Baulny H, Touati G, Prokisch H, Lombès A. Kremer LS, et al. Among authors: meitinger t. J Hepatol. 2016 Aug;65(2):377-85. doi: 10.1016/j.jhep.2016.04.017. Epub 2016 May 2. J Hepatol. 2016. PMID: 27151179 Free PMC article.

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

The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted.

Grabowski M, Zimprich A, Lorenz-Depiereux B, Kalscheuer V, Asmus F, Gasser T, Meitinger T, Strom TM. Grabowski M, et al. Among authors: meitinger t. Eur J Hum Genet. 2003 Feb;11(2):138-44. doi: 10.1038/sj.ejhg.5200938. Eur J Hum Genet. 2003. PMID: 12634861

4

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.

5

A gene locus responsible for the familial hair shaft abnormality pili annulati maps to chromosome 12q24.32-24.33.

Giehl KA, Eckstein GN, Benet-Pagès A, Tosti A, de Berker DA, Meitinger T, Müller-Myhsok B, Strom TM. Giehl KA, et al. Among authors: meitinger t. J Invest Dermatol. 2004 Dec;123(6):1073-7. doi: 10.1111/j.0022-202X.2004.23423.x. J Invest Dermatol. 2004. PMID: 15610517 Free article.

6

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

7

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

8

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

9

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

10

Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation.

Wagenstaller J, Spranger S, Lorenz-Depiereux B, Kazmierczak B, Nathrath M, Wahl D, Heye B, Glaser D, Liebscher V, Meitinger T, Strom TM. Wagenstaller J, et al. Among authors: meitinger t. Am J Hum Genet. 2007 Oct;81(4):768-79. doi: 10.1086/521274. Epub 2007 Aug 28. Am J Hum Genet. 2007. PMID: 17847001 Free PMC article.

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