Search Results - Holger Prokisch

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  1. 1
    MitoP2: the mitochondrial proteome database--now including mouse data

    MitoP2: the mitochondrial proteome database--now including mouse data by Holger Prokisch

    Published 2005
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  2. 2
    Mitochondria: Much ado about nothing? How dangerous is reactive oxygen species production?

    Mitochondria: Much ado about nothing? How dangerous is reactive oxygen species production? by Eliška Holzerová, Holger Prokisch

    Published 2015
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  3. 3
    ncRNAs: New Players in Mitochondrial Health and Disease?

    ncRNAs: New Players in Mitochondrial Health and Disease? by Mirjana Gušić, Holger Prokisch

    Published 2020
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  4. 4
    Genetics of mitochondrial diseases: Identifying mutations to help diagnosis

    Genetics of mitochondrial diseases: Identifying mutations to help diagnosis by Sarah L. Stenton, Holger Prokisch

    Published 2020
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  5. 5
    The Dimensions of Primary Mitochondrial Disorders

    The Dimensions of Primary Mitochondrial Disorders by Lea D. Schlieben, Holger Prokisch

    Published 2020
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  6. 6
    “Transcriptomics”: molecular diagnosis of inborn errors of metabolism via RNA‐sequencing

    “Transcriptomics”: molecular diagnosis of inborn errors of metabolism via RNA‐sequencing by Laura S. Kremer, Saskia B. Wortmann, Holger Prokisch

    Published 2018
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  7. 7
    Mitochondrial disorders

    Mitochondrial disorders by Thomas Klopstock, Claudia Priglinger, Ali Yılmaz, Cornelia Kornblum, Felix Distelmaier, Holger Prokisch

    Published 2021
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  8. 8
    Treatable mitochondrial diseases: cofactor metabolism and beyond

    Treatable mitochondrial diseases: cofactor metabolism and beyond by Felix Distelmaier, Tobias B. Haack, Saskia B. Wortmann, Johannes A. Mayr, Holger Prokisch

    Published 2016
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  9. 9
    The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi‐omic pipelines

    The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi‐omic pipelines by Charlotte L. Alston, Sarah L. Stenton, Gavin Hudson, Holger Prokisch, Robert W. Taylor

    Published 2021
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  10. 10
    Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca2+

    Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress a... by Paola Venco, Massimo Bonora, Carlotta Giorgi, Elena Papaleo, Arcangela Iuso, Holger Prokisch, Paolo Pinton, Valeria Tiranti

    Published 2015
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  11. 11
    Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease

    Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease by Tobias B. Haack, Dirk Klee, Tim M. Strom, Ertan Mayatepek, Thomas Meitinger, Holger Prokisch, Felix Distelmaier

    Published 2014
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  12. 12
    Aberrant splicing prediction across human tissues

    Aberrant splicing prediction across human tissues by Nils Wagner, Muhammed Hasan Çelik, Florian R. Hölzlwimmer, Christian Mertes, Holger Prokisch, Vicente A. Yépez, Julien Gagneur

    Published 2023
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  13. 13
    A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1

    A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1 by Eva Lattka, Stefanie Eggers, Gabriele Moeller, Katharina Heim, Malory Weber, Divya Mehta, Holger Prokisch, Thomas Illig, Jerzy Adamski

    Published 2009
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  14. 14
    Assessing Systems Properties of Yeast Mitochondria through an Interaction Map of the Organelle

    Assessing Systems Properties of Yeast Mitochondria through an Interaction Map of the Organelle by Fabiana Perocchi, Lars Juhl Jensen, Julien Gagneur, Uwe Ahting, Christian von Mering, Peer Bork, Holger Prokisch, Lars M. Steinmetz

    Published 2006
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  15. 15
    OUTRIDER: A Statistical Method for Detecting Aberrantly Expressed Genes in RNA Sequencing Data

    OUTRIDER: A Statistical Method for Detecting Aberrantly Expressed Genes in RNA Sequencing Data by Felix Brechtmann, Christian Mertes, Agnė Matusevičiūtė, Vicente A. Yépez, Žiga Avsec, Maximilian Herzog, Daniel M. Bader, Holger Prokisch, Julien Gagneur

    Published 2018
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  16. 16
    The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity

    The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity by Christian Johannes Gloeckner, Norbert Kinkl, Annette Schumacher, Ralf J. Braun, Eric O’Neill, Thomas Meitinger, Walter Kölch, Holger Prokisch, Marius Ueffing

    Published 2005
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  17. 17
    OCR-Stats: Robust estimation and statistical testing of mitochondrial respiration activities using Seahorse XF Analyzer

    OCR-Stats: Robust estimation and statistical testing of mitochondrial respiration activities using Seahorse XF Analyzer by Vicente A. Yépez, Laura S. Kremer, Arcangela Iuso, Mirjana Gušić, Robert Kopajtich, Eliška Koňaříková, Agnieszka Nadel, Leonhard Wachutka, Holger Prokisch, Julien Gagneur

    Published 2018
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  18. 18
    Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases

    Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases by Jing Tan, Matias Wagner, Sarah L. Stenton, Tim M. Strom, Saskia B. Wortmann, Holger Prokisch, Thomas Meitinger, Konrad Oexle, Thomas Klopstock

    Published 2020
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  19. 19
    Detection of aberrant splicing events in RNA-seq data using FRASER

    Detection of aberrant splicing events in RNA-seq data using FRASER by Christian Mertes, Ines F. Scheller, Vicente A. Yépez, Muhammed Hasan Çelik, Yingjiqiong Liang, Laura S. Kremer, Mirjana Gušić, Holger Prokisch, Julien Gagneur

    Published 2021
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  20. 20
    Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9

    Fatal neonatal encephalopathy and lactic acidosis caused by a homozygous loss-of-function variant in COQ9 by Katharina Danhauser, Diran Herebıan, Tobias B. Haack, Richard J. Rodenburg, Tim M. Strom, Thomas Meitinger, Dirk Klee, Ertan Mayatepek, Holger Prokisch, Felix Distelmaier

    Published 2015
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