Year |
Citation |
Score |
2021 |
Berndt N, Kolbe E, Gajowski R, Eckstein J, Ott F, Meierhofer D, Holzhütter HG, Matz-Soja M. Functional Consequences of Metabolic Zonation in Murine Livers: Insights for an Old Story. Hepatology (Baltimore, Md.). 73: 795-810. PMID 32286709 DOI: 10.1002/Hep.31274 |
0.321 |
|
2020 |
Xiao Y, Clima R, Busch J, Rabien A, Kilic E, Villegas SL, Timmermann B, Attimonelli M, Jung K, Meierhofer D. Decreased mitochondrial DNA content drives OXPHOS dysregulation in chromophobe renal cell carcinoma. Cancer Research. PMID 32694149 DOI: 10.1158/0008-5472.Can-20-0754 |
0.385 |
|
2019 |
Kolbe E, Aleithe S, Rennert C, Spormann L, Ott F, Meierhofer D, Gajowski R, Stöpel C, Hoehme S, Kücken M, Brusch L, Seifert M, von Schoenfels W, Schafmayer C, Brosch M, et al. Mutual Zonated Interactions of Wnt and Hh Signaling Are Orchestrating the Metabolism of the Adult Liver in Mice and Human. Cell Reports. 29: 4553-4567.e7. PMID 31875560 DOI: 10.1016/J.Celrep.2019.11.104 |
0.322 |
|
2019 |
Sen NE, Arsovic A, Meierhofer D, Brodesser S, Oberschmidt C, Canet-Pons J, Kaya ZE, Halbach MV, Gispert S, Sandhoff K, Auburger G. In Human and Mouse Spino-Cerebellar Tissue, Ataxin-2 Expansion Affects Ceramide-Sphingomyelin Metabolism. International Journal of Molecular Sciences. 20. PMID 31766565 DOI: 10.3390/Ijms20235854 |
0.335 |
|
2019 |
Ni Y, Hagras MA, Konstantopoulou V, Mayr JA, Stuchebrukhov AA, Meierhofer D. Mutations in Cause Metabolic Reprogramming and Disruption of the Electron Transfer. Cells. 8. PMID 31557978 DOI: 10.3390/Cells8101149 |
0.539 |
|
2019 |
Al Ahmad A, Paffrath V, Clima R, Busch JF, Rabien A, Kilic E, Villegas S, Timmermann B, Attimonelli M, Jung K, Meierhofer D. Papillary Renal Cell Carcinomas Rewire Glutathione Metabolism and Are Deficient in Both Anabolic Glucose Synthesis and Oxidative Phosphorylation. Cancers. 11. PMID 31484429 DOI: 10.3390/Cancers11091298 |
0.323 |
|
2019 |
Sen NE, Canet-Pons J, Halbach MV, Arsovic A, Pilatus U, Chae WH, Kaya ZE, Seidel K, Rollmann E, Mittelbronn M, Meierhofer D, De Zeeuw CI, Bosman LWJ, Gispert S, Auburger G. Generation of an Atxn2-CAG100 knock-in mouse reveals N-acetylaspartate production deficit due to early Nat8l dysregulation. Neurobiology of Disease. 104559. PMID 31376479 DOI: 10.1016/J.Nbd.2019.104559 |
0.326 |
|
2019 |
Berndt N, Eckstein J, Heucke N, Gajowski R, Stockmann M, Meierhofer D, Holzhütter HG. Characterization of Lipid and Lipid Droplet Metabolism in Human HCC. Cells. 8. PMID 31137921 DOI: 10.3390/Cells8050512 |
0.308 |
|
2018 |
Berndt N, Bulik S, Wallach I, Wünsch T, König M, Stockmann M, Meierhofer D, Holzhütter HG. HEPATOKIN1 is a biochemistry-based model of liver metabolism for applications in medicine and pharmacology. Nature Communications. 9: 2386. PMID 29921957 DOI: 10.1038/S41467-018-04720-9 |
0.329 |
|
2017 |
Kürschner G, Zhang Q, Clima R, Xiao Y, Busch JF, Kilic E, Jung K, Berndt N, Bulik S, Holzhütter HG, Gasparre G, Attimonelli M, Babu M, Meierhofer D. Renal oncocytoma characterized by the defective complex I of the respiratory chain boosts the synthesis of the ROS scavenger glutathione. Oncotarget. 8: 105882-105904. PMID 29285300 DOI: 10.18632/Oncotarget.22413 |
0.354 |
|
2017 |
Torres-Odio S, Key J, Hoepken HH, Canet-Pons J, Valek L, Roller B, Walter M, Morales-Gordo B, Meierhofer D, Harter PN, Mittelbronn M, Tegeder I, Gispert S, Auburger G. Progression of pathology in PINK1-deficient mouse brain from splicing via ubiquitination, ER stress, and mitophagy changes to neuroinflammation. Journal of Neuroinflammation. 14: 154. PMID 28768533 DOI: 10.1186/S12974-017-0928-0 |
0.305 |
|
2017 |
Auburger G, Sen NE, Meierhofer D, Başak AN, Gitler AD. Efficient Prevention of Neurodegenerative Diseases by Depletion of Starvation Response Factor Ataxin-2. Trends in Neurosciences. PMID 28684172 DOI: 10.1016/J.Tins.2017.06.004 |
0.345 |
|
2017 |
Medina AB, Banaszczak M, Ni Y, Aretz I, Meierhofer D. ρ⁰ Cells Feature De-Ubiquitination of SLC Transporters and Increased Levels and Fluxes of Amino Acids. International Journal of Molecular Sciences. 18. PMID 28425971 DOI: 10.3390/Ijms18040879 |
0.517 |
|
2017 |
Lorenz C, Lesimple P, Bukowiecki R, Zink A, Inak G, Mlody B, Singh M, Semtner M, Mah N, Auré K, Leong M, Zabiegalov O, Lyras EM, Pfiffer V, Fauler B, ... ... Meierhofer D, et al. Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders. Cell Stem Cell. PMID 28132834 DOI: 10.1016/J.Stem.2016.12.013 |
0.335 |
|
2016 |
Seidel G, Meierhofer D, Sen NE, Guenther A, Krobitsch S, Auburger G. Quantitative global proteomics of yeast PBP1 deletion mutants and their stress responses identifies glucose metabolism, mitochondrial, and stress granule changes. Journal of Proteome Research. PMID 27966978 DOI: 10.1021/Acs.Jproteome.6B00647 |
0.335 |
|
2016 |
Knierim E, Hirata H, Wolf NI, Morales-Gonzalez S, Schottmann G, Tanaka Y, Rudnik-Schöneborn S, Orgeur M, Zerres K, Vogt S, van Riesen A, Gill E, Seifert F, Zwirner A, Kirschner J, ... ... Meierhofer D, et al. Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures. American Journal of Human Genetics. PMID 26924529 DOI: 10.1016/J.Ajhg.2016.01.006 |
0.307 |
|
2016 |
Aretz I, Hardt C, Wittig I, Meierhofer D. An Impaired Respiratory Electron Chain Triggers Down-regulation of the Energy Metabolism and De-ubiquitination of Solute Carrier Amino Acid Transporters. Molecular & Cellular Proteomics : McP. 15: 1526-38. PMID 26852163 DOI: 10.1074/Mcp.M115.053181 |
0.389 |
|
2016 |
Meierhofer D, Halbach M, Sen NE, Gispert S, Auburger G. Atxn2-Knock-Out mice show branched chain amino acids and fatty acids pathway alterations. Molecular & Cellular Proteomics : McP. PMID 26850065 DOI: 10.1074/Mcp.M115.056770 |
0.36 |
|
2015 |
Correia JC, Massart J, de Boer JF, Porsmyr-Palmertz M, Martínez-Redondo V, Agudelo LZ, Sinha I, Meierhofer D, Ribeiro V, Björnholm M, Sauer S, Dahlman-Wright K, Zierath JR, Groen AK, Ruas JL. Bioenergetic cues shift FXR splicing towards FXRα2 to modulate hepatic lipolysis and fatty acid metabolism. Molecular Metabolism. 4: 891-902. PMID 26909306 DOI: 10.1016/J.Molmet.2015.09.005 |
0.32 |
|
2015 |
Fischer-Zirnsak B, Escande-Beillard N, Ganesh J, Tan YX, Al Bughaili M, Lin AE, Sahai I, Bahena P, Reichert SL, Loh A, Wright GD, Liu J, Rahikkala E, Pivnick EK, Choudhri AF, ... ... Meierhofer D, et al. Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa. American Journal of Human Genetics. 97: 483-92. PMID 26320891 DOI: 10.1016/J.Ajhg.2015.08.001 |
0.342 |
|
2015 |
Egerer J, Emmerich D, Fischer-Zirnsak B, Chan WL, Meierhofer D, Tuysuz B, Marschner K, Sauer S, Barr FA, Mundlos S, Kornak U. GORAB Missense Mutations Disrupt RAB6 and ARF5 Binding and Golgi Targeting. The Journal of Investigative Dermatology. 135: 2368-2376. PMID 26000619 DOI: 10.1038/Jid.2015.192 |
0.3 |
|
2015 |
Gielisch I, Meierhofer D. Metabolome and proteome profiling of complex I deficiency induced by rotenone. Journal of Proteome Research. 14: 224-35. PMID 25361611 DOI: 10.1021/Pr500894V |
0.354 |
|
2014 |
Meierhofer D, Weidner C, Sauer S. Integrative analysis of transcriptomics, proteomics, and metabolomics data of white adipose and liver tissue of high-fat diet and rosiglitazone-treated insulin-resistant mice identified pathway alterations and molecular hubs. Journal of Proteome Research. 13: 5592-602. PMID 25287014 DOI: 10.1021/Pr5005828 |
0.339 |
|
2013 |
Meierhofer D, Weidner C, Hartmann L, Mayr JA, Han CT, Schroeder FC, Sauer S. Protein sets define disease states and predict in vivo effects of drug treatment. Molecular & Cellular Proteomics : McP. 12: 1965-79. PMID 23579186 DOI: 10.1074/Mcp.M112.025031 |
0.322 |
|
2011 |
Mayr JA, Zimmermann FA, Fauth C, Bergheim C, Meierhofer D, Radmayr D, Zschocke J, Koch J, Sperl W. Lipoic acid synthetase deficiency causes neonatal-onset epilepsy, defective mitochondrial energy metabolism, and glycine elevation. American Journal of Human Genetics. 89: 792-7. PMID 22152680 DOI: 10.1016/J.Ajhg.2011.11.011 |
0.354 |
|
2008 |
Mayr JA, Meierhofer D, Zimmermann F, Feichtinger R, Kögler C, Ratschek M, Schmeller N, Sperl W, Kofler B. Loss of complex I due to mitochondrial DNA mutations in renal oncocytoma. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 14: 2270-5. PMID 18413815 DOI: 10.1158/1078-0432.Ccr-07-4131 |
0.367 |
|
2006 |
Wiesbauer M, Meierhofer D, Mayr JA, Sperl W, Paulweber B, Kofler B. Multiplex primer extension analysis for rapid detection of major European mitochondrial haplogroups. Electrophoresis. 27: 3864-8. PMID 16960846 DOI: 10.1002/Elps.200600086 |
0.313 |
|
2006 |
Meierhofer D, Mayr JA, Fink K, Schmeller N, Kofler B, Sperl W. Mitochondrial DNA mutations in renal cell carcinomas revealed no general impact on energy metabolism British Journal of Cancer. 94: 268-274. PMID 16404428 DOI: 10.1038/Sj.Bjc.6602929 |
0.357 |
|
2006 |
Meierhofer D, Ebner S, Mayr JA, Jones ND, Kofler B, Sperl W. Platelet transfusion can mimic somatic mtDNA mutations Leukemia. 20: 362-363. PMID 16357835 DOI: 10.1038/Sj.Leu.2404070 |
0.313 |
|
2005 |
Meierhofer D, Mayr JA, Ebner S, Sperl W, Kofler B. Rapid screening of the entire mitochondrial DNA for low-level heteroplasmic mutations. Mitochondrion. 5: 282-96. PMID 16050991 DOI: 10.1016/J.Mito.2005.06.001 |
0.327 |
|
2004 |
Meierhofer D, Mayr JA, Foetschl U, Berger A, Fink K, Schmeller N, Hacker GW, Hauser-Kronberger C, Kofler B, Sperl W. Decrease of mitochondrial DNA content and energy metabolism in renal cell carcinoma. Carcinogenesis. 25: 1005-10. PMID 14764459 DOI: 10.1093/Carcin/Bgh104 |
0.319 |
|
2003 |
Berger A, Mayr JA, Meierhofer D, Fötschl U, Bittner R, Budka H, Grethen C, Huemer M, Kofler B, Sperl W. Severe depletion of mitochondrial DNA in spinal muscular atrophy. Acta Neuropathologica. 105: 245-51. PMID 12557011 DOI: 10.1007/S00401-002-0638-1 |
0.304 |
|
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