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Holger Prokisch

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Julia Mayerle; Matthias Nauck; Marjolein J Peters; Holger Prokisch; Fernando Rivadeneira; Claudia Schurmann; Ivo Steinmetz; Lisette Stolk; Alexander Teumer; Andre G Uitterlinden; Joyce B J van Meurs; Uwe Völker; Henry Völzke; Frank-Ulrich Weiss; Martin Zenker; Kathrin Zimmermann; Lisette G Capelle; Annemarie C de Vries; Caroline M den Hoed; Florian Ernst; Sybille Gruska; Albert Hofman; Georg Homuth; Heyo K Kroemer; Markus M Lerch; Ernst Kuipers
Identification of genetic loci associated with Helicobacter pylori serologic status.
Konrad Oexle; Annette Peters; Holger Prokisch; Janina S Ried; Barbara Schormair; Michael Specht; Joachim Thiery; Claudia Trenkwalder; H-Erich Wichmann; Darina Czamara; Angela Döring; Birgit Frauscher; Christian Gieger; Katharina Heim; Birgit Högl; Peter Lichtner; G Martin Fiedler; Thomas Meitinger; Bertram Müller-Myhsok; Juliane Winkelmann
Dilution of candidates: the case of iron-related genes in restless legs syndrome.
Eva C Schulte; Juliane Winkelmann; Angela Jochim; Holger Prokisch; Malte C Claussen; Annette Förschler; Tobias Haack; Monika Hartig; Ursula Haun-Jünger; Bernhard Hemmer; Maja Hempel; Rüdiger Ilg
Mitochondrial membrane protein associated neurodegenration: a novel variant of neurodegeneration with brain iron accumulation.

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2013: Julia Mayerle; Matthias Nauck; Marjolein J Peters; Holger Prokisch; Fernando Rivadeneira; Claudia Schurmann; Ivo Steinmetz; Lisette Stolk; Alexander Teumer; Andre G Uitterlinden; Joyce B J van Meurs; Uwe Völker; Henry Völzke; Frank-Ulrich Weiss; Martin Zenker; Kathrin Zimmermann; Lisette G Capelle; Annemarie C de Vries; Caroline M den Hoed; Florian Ernst; Sybille Gruska; Albert Hofman; Georg Homuth; Heyo K Kroemer; Markus M Lerch; Ernst Kuipers
Identification of genetic loci associated with Helicobacter pylori serologic status.
JAMA : the journal of the American Medical Association 2013;309(18):1912-20.
2013: Konrad Oexle; Annette Peters; Holger Prokisch; Janina S Ried; Barbara Schormair; Michael Specht; Joachim Thiery; Claudia Trenkwalder; H-Erich Wichmann; Darina Czamara; Angela Döring; Birgit Frauscher; Christian Gieger; Katharina Heim; Birgit Högl; Peter Lichtner; G Martin Fiedler; Thomas Meitinger; Bertram Müller-Myhsok; Juliane Winkelmann
Dilution of candidates: the case of iron-related genes in restless legs syndrome.
European journal of human genetics : EJHG 2013;21(4):410-4.
2013: Eva C Schulte; Juliane Winkelmann; Angela Jochim; Holger Prokisch; Malte C Claussen; Annette Förschler; Tobias Haack; Monika Hartig; Ursula Haun-Jünger; Bernhard Hemmer; Maja Hempel; Rüdiger Ilg
Mitochondrial membrane protein associated neurodegenration: a novel variant of neurodegeneration with brain iron accumulation.
Movement disorders : official journal of the Movement Disorder Society 2013;28(2):224-7.
2013: Cornelia Kornblum; Wolfram S Kunz; Thomas Meitinger; Michal Minczuk; Maurizio Moggio; Vamsi K Mootha; Thomas J Nicholls; Viktoriya Peeva; Sarah E Calvo; Giacomo P Comi; Katharina Danhauser; Salvatore DiMauro; Tobias B Haack; Kerstin Hallmann; Arcangela Iuso; Thomas Klopstock; Catarina M Quinzii; Dario Ronchi; Joanna Rorbach; Susanne Schöler; Monica Sciacco; Tim M Strom; Thomas Wieland; Gabor Zsurka; Holger Prokisch
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease.
Nature genetics 2013;45(2):214-9.
2013: Divya Mehta; Thomas Meitinger; Matthias Nauck; Maren Carstensen; Gertrud Eckstein; Christian Gieger; Katharina Heim; Christian Herder; Georg Homuth; Thomas Illig; Michael Roden; Claudia Schurmann; Uwe Völker; Holger Prokisch
Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood.
European journal of human genetics : EJHG 2013;21(1):48-54.
2013: Tobias B Haack; Birgit Haberberger; Thomas Hoppen; Johannes A Mayr; Thomas Meitinger; B Rolinski; Jessica Schum; Wolfgang Sperl; Valentina Strecker; Tim M Strom; Ilka Wittig; Franz Zimmermann; Uwe Athing; Peter Freisinger; Elisabeth Graf; Holger Prokisch
Homozygous missense mutation in BOLA3 causes multiple mitochondrial dysfunctions syndrome in two siblings.
Journal of inherited metabolic disease 2013;36(1):55-62.
2012: Katharina Danhauser; Elisabeth Graf; Tobias B Haack; Georg F Hoffmann; Thomas Meitinger; Jürgen G Okun; Holger Prokisch; Sven W Sauer; Christian Staufner; Tim M Strom; Thorsten Traub; Thomas Wieland; Johannes Zschocke; Stefan Kölker
DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduria.
American journal of human genetics 2012;91(6):1082-7.
2012: Tobias B Haack; Maja Hempel; Ken Inui; Christine Makowski; Johannes A Mayr; Thomas Meitinger; Tim M Strom; Ulrike Tauer; Thomas Wieland; Yoshiaki Yao; Atsushi Yonezawa; Hiroki Yoshimatsu; Uwe Ahting; Peter Freisinger; Elisabeth Graf; Holger Prokisch
Impaired riboflavin transport due to missense mutations in SLC52A2 causes Brown-Vialetto-Van Laere syndrome.
Journal of inherited metabolic disease 2012;35(6):943-8.
2012: Monika B Hartig; Thomas Meitinger; Holger Prokisch; Thomas Klopstock
Pantothenate kinase-associated neurodegeneration.
Current drug targets 2012;13(9):1182-9.
2012: Daniele Ghezzi; Tobias B Haack; Federica Invernizzi; Thomas Meitinger; Laura Melchionda; Rossella Parini; Holger Prokisch; Tim M Strom; Enrico Baruffini; Alberto B Burlina; Cristina Dallabona; Ileana Ferrero; Massimo Zeviani
Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosis.
American journal of human genetics 2012;90(6):1079-87.
2012: Marjan E Steenweg; Tim M Strom; Johann Te Water Naudé; Carola G M van Berkel; Marjo S van der Knaap; Truus E M Abbink; Enrico Bertini; Annette Bley; Luisa Diogo; Daniele Ghezzi; Eugenio Grillo; Tobias Haack; Diego Martinelli; Holger Prokisch; Massimo Zeviani
Leukoencephalopathy with thalamus and brainstem involvement and high lactate 'LTBL' caused by EARS2 mutations.
Brain : a journal of neurology 2012;135(Pt 5):1387-94.
2012: Tobias B Haack; Birgit Haberberger; Hana Hansikova; Julia B Hennermann; Ulrike Herberg; Georg F Hoffmann; Arcangela Iuso; Thomas Klopstock; Klaus A Kuhn; Johannes A Mayr; Thomas Meitinger; Barbara Plecko; Markus Schuelke; Wolfgang Sperl; Valentina Strecker; Tim M Strom; Marketa Tesarova; Thomas Wieland; Ekkehard Wilichowski; Ilka Wittig; Jiri Zeman; Massimo Zeviani; Uwe Ahting; Peter Freisinger; Eva-Maria Frisch; Matteo Gorza; Elisabeth Graf; Holger Prokisch
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
Journal of medical genetics 2012;49(4):277-83.
2012: Johannes A Mayr; Thomas Meitinger; Isabella Moroni; Matthias R Baumgartner; Elisabeth Graf; Tobias B Haack; Birgit Haberberger; Janbernd Kirschner; Eleonora Lamantea; Richard J Rodenburg; Jan Smeitink; Wolfgang Sperl; Beat Steinmann; Tim M Strom; Andrea Superti-Furga; Thomas Wieland; Massimo Zeviani; Franz A Zimmermann; Holger Prokisch
Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome.
American journal of human genetics 2012;90(2):314-20.
2012: Homa Attar; Karen Bedard; Christelle Borel; jean maurice delabar; Emmanouil T Dermitzakis; Patrick Descombes; Samuel Deutsch; Yann Dupré; Maryline Gagnebin; Karl-Heinz Krause; Divya Mehta; Thomas Meitinger; Eugenia Migliavacca; Holger Prokisch; Erich Wichmann; Stylianos E Antonarakis
Extensive natural variation for cellular hydrogen peroxide release is genetically controlled.
PloS one 2012;7(8):e43566.
2011: Monika B Hartig; Katharina Heim; Maja Hempel; Arcangela Iuso; Sergiusz Jozwiak; Elzbieta Jurkiewicz; Thomas Klopstock; Tomasz Kmiec; Malgorzata Krajewska-Walasek; Hans A Kretzschmar; Thomas Meitinger; Wolfgang Mueller-Felber; Konrad Oexle; Sabrina Dusi; Matthias Elstner; Thomas Gasser; Tobias Haack; Sigrun Roeber; Gerd Schmitz; Tim M Strom; Victoria Tarabin; Valeria Tiranti; Claudia Trenkwalder; Juliane Winkelmann; Holger Prokisch
Absence of an orphan mitochondrial protein, c19orf12, causes a distinct clinical subtype of neurodegeneration with brain iron accumulation.
American journal of human genetics 2011;89(4):543-50.
2011: Matthias Elstner; Katharina Heim; Evelyn Jaros; Thomas Klopstock; Divya Mehta; Thomas Meitinger; Christopher M Morris; Andreas Bender; Douglass M Turnbull; Holger Prokisch
Expression analysis of dopaminergic neurons in Parkinson's disease and aging links transcriptional dysregulation of energy metabolism to cell death.
Acta neuropathologica 2011;122(1):75-86.
2011: Katharina Danhauser; Arcangela Iuso; Tobias B Haack; Peter Freisinger; Knut Brockmann; Johannes A Mayr; Thomas Meitinger; Holger Prokisch
Cellular rescue-assay aids verification of causative DNA-variants in mitochondrial complex I deficiency.
Molecular genetics and metabolism 2011;103(2):161-6.
2011: Matthias Elstner; Thomas Klopstock; Lena Krieg; Christoph Laub; Lars Leidolt; Birgit Liss; Eliezer Masliah; Chris Morris; Sarina K Müller; Holger Prokisch; Falk Schlaudraff; Douglass M Turnbull; Andreas Bender
Neuromelanin, neurotransmitter status and brainstem location determine the differential vulnerability of catecholaminergic neurons to mitochondrial DNA deletions.
Molecular brain 2011;4():43.
2011: Mike Gerards; Bianca J C van den Bosch; Katharina Danhauser; Valérie Serre; Michel van Weeghel; Ronald J A Wanders; Gerry A F Nicolaes; Wim Sluiter; Kees Schoonderwoerd; Hans R Scholte; Holger Prokisch; Agnès Rötig; I F M de Coo; H J M Smeets
Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene.
Brain : a journal of neurology 2011;134(Pt 1):210-9.
2010: Georg Winterer; Kirstin Mittelstrass; Ina Giegling; Claudia Lamina; Christoph Fehr; Hermann Brenner; Lutz P Breitling; Barbara Nitz; Elke Raum; Heiko Müller; Jürgen Gallinat; Andreas Gal; Katharina Heim; Holger Prokisch; Thomas Meitinger; Annette M Hartmann; Hans-Jürgen Möller; Christian Gieger; H-Erich Wichmann; Thomas Illig; Norbert Dahmen; Dan Rujescu
Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(8):1448-58.
2010: Tobias B Haack; Katharina Danhauser; Birgit Haberberger; Jonathan Hoser; Valentina Strecker; Detlef Boehm; Graziella Uziel; Eleonora Lamantea; Federica Invernizzi; Joanna Poulton; Boris Rolinski; Arcangela Iuso; Saskia Biskup; Thorsten Schmidt; Hans-Werner Mewes; Ilka Wittig; Thomas Meitinger; Massimo Zeviani; Holger Prokisch
Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency.
Nature genetics 2010;42(12):1131-4.
2010: Carola Marzi; Eva Albrecht; Pirro G Hysi; Vasiliki Lagou; Melanie Waldenberger; Anke Tönjes; Inga Prokopenko; Katharina Heim; Hannah Blackburn; Janina S Ried; Marcus E Kleber; Massimo Mangino; Barbara Thorand; Annette Peters; Christopher J Hammond; Harald Grallert; Bernhard O Boehm; Peter Kovacs; Ludwig Geistlinger; Holger Prokisch; Bernhard R Winkelmann; Tim D Spector; H-Erich Wichmann; Michael Stumvoll; Nicole Soranzo; Winfried März; Wolfgang Koenig; Thomas Illig; Christian Gieger
Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.
PLoS genetics 2010;6(11):e1001213.
2010: Patrick Linsel-Nitschke; Jörg Heeren; Zouhair Aherrahrou; Petra Bruse; Christian Gieger; Thomas Illig; Holger Prokisch; Katharina Heim; Angela Doering; Annette Peters; Thomas Meitinger; H-Erich Wichmann; Anke Hinney; Thomas Reinehr; Christian Roth; Jan R Ortlepp; Mouhidien Soufi; Alexander M Sattler; Jürgen Schaefer; Klaus Stark; Christian Hengstenberg; Arne Schaefer; Stefan Schreiber; Florian Kronenberg; Nilesh J Samani; Heribert Schunkert; Jeanette Erdmann
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.
Atherosclerosis 2010;208(1):183-9.
2010: E Lattka; S Eggers; G Moeller; K Heim; M Weber; D Mehta; Holger Prokisch; T Illig; J Adamski
A common FADS2 promoter polymorphism increases promoter activity and facilitates binding of transcription factor ELK1.
Journal of lipid research 2010;51(1):182-91.
2009: Daniele Ghezzi; Paola Goffrini; Graziella Uziel; Rita Horvath; Thomas Klopstock; Hanns Lochmüller; Pio D'Adamo; Paolo Gasparini; Tim M Strom; Holger Prokisch; Federica Invernizzi; Ileana Ferrero; Massimo Zeviani
SDHAF1, encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy.
Nature genetics 2009;41(6):654-6.
2009: Uwe Ahting; Thomas Floss; Nikolas Uez; Ilka Schneider-Lohmar; Lore Becker; Eva Kling; Arcangela Iuso; Andreas Bender; Martin Hrabé De Angelis; Valérie Gailus-Durner; Helmut Fuchs; Thomas Meitinger; Wolfgang Wurst; Holger Prokisch; Thomas Klopstock
Neurological phenotype and reduced lifespan in heterozygous Tim23 knockout mice, the first mouse model of defective mitochondrial import.
Biochimica et biophysica acta 2009;1787(5):371-6.
2009: Nicole Soranzo; Augusto Rendon; Christian Gieger; Chris I Jones; Nicholas A Watkins; Stephan Menzel; Angela Döring; Jonathan Stephens; Holger Prokisch; Wendy Erber; Simon C Potter; Sarah L Bray; Philippa Burns; Jennifer Jolley; Mario Falchi; Brigitte Kühnel; Jeanette Erdmann; Heribert Schunkert; Nilesh J Samani; Thomas Illig; Stephen F Garner; Angela Rankin; Christa Meisinger; John R Bradley; Swee Lay Thein; Alison H Goodall; Tim D Spector; Panos Deloukas; Willem H Ouwehand
A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function.
Blood 2009;113(16):3831-7.
2009: Matthias Elstner; C Andreoli; Thomas Klopstock; Thomas Meitinger; Holger Prokisch
The mitochondrial proteome database: MitoP2.
Methods in enzymology 2009;457():3-20.
2009: Christa Meisinger; Holger Prokisch; Christian Gieger; Nicole Soranzo; Divya Mehta; Dieter Rosskopf; Peter Lichtner; Norman Klopp; Jonathan Stephens; Nicholas A Watkins; Panos Deloukas; Andreas Greinacher; Wolfgang Koenig; Matthias Nauck; Christian Rimmbach; Henry Völzke; Annette Peters; Thomas Illig; Willem H Ouwehand; Thomas Meitinger; H-Erich Wichmann; Angela Döring
A genome-wide association study identifies three loci associated with mean platelet volume.
American journal of human genetics 2009;84(1):66-71.
2008: Tobias Birnbaum; H J Blom; Holger Prokisch; M Hartig; Thomas Klopstock
Methylenetetrahydrofolate reductase deficiency (homocystinuria type II) as a rare cause of rapidly progressive tetraspasticity and psychosis in a previously healthy adult.
Journal of neurology 2008;255(11):1845-6.
2008: Matthias Elstner; Christophe Andreoli; Uwe Ahting; Igor Tetko; Thomas Klopstock; Thomas Meitinger; Holger Prokisch
MitoP2: an integrative tool for the analysis of the mitochondrial proteome.
Molecular biotechnology 2008;40(3):306-15.
2008: Angela Döring; Christian Gieger; Divya Mehta; Henning Gohlke; Holger Prokisch; Stefan Coassin; Guido Fischer; Kathleen Henke; Norman Klopp; Florian Kronenberg; Bernhard Paulweber; Arne Pfeufer; Dieter Rosskopf; Henry Völzke; Thomas Illig; Thomas Meitinger; H-Erich Wichmann; Christa Meisinger
SLC2A9 influences uric acid concentrations with pronounced sex-specific effects.
Nature genetics 2008;40(4):430-6.
2008: Chul Hyoung Lyoo; Holger Prokisch; Thomas Meitinger; Seung Yeob Lee; Do Hyoun Kim; Myung Sik Lee
Anticholinergic-responsive gait freezing in a patient with pantothenate kinase-associated neurodegeneration.
Movement disorders : official journal of the Movement Disorder Society 2008;23(2):283-4.
2007: Holger Prokisch; Monika Hartig; Rosa Hellinger; Thomas Meitinger; Thomas Rosenberg
A population-based epidemiological and genetic study of X-linked retinitis pigmentosa.
Investigative ophthalmology & visual science 2007;48(9):4012-8.
2007: Klaus Gempel; Haluk Topaloglu; Beril Talim; Peter Schneiderat; Benedikt Schoser; Volkmar H Hans; Beatrix Pálmafy; Gülsev Kale; Aysegul Tokatli; Catarina M Quinzii; Michio Hirano; Ali Naini; Salvatore DiMauro; Holger Prokisch; Hanns Lochmüller; Rita Horvath
The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene.
Brain : a journal of neurology 2007;130(Pt 8):2037-44.
2007: Holger Prokisch; Uwe Ahting
MitoP2, an integrated database for mitochondrial proteins.
Methods in molecular biology (Clifton, N.J.) 2007;372():573-86.
2006: Fabiana Perocchi; Lars Jensen; Julien Gagneur; Uwe Ahting; Christian von Mering; Peer Bork; Holger Prokisch; Lars M Steinmetz
Assessing systems properties of yeast mitochondria through an interaction map of the organelle.
PLoS genetics 2006;2(10):e170.
2006: Rita Horvath; Gavin Hudson; Gianfrancesco Ferrari; Nancy Fütterer; Sofia Ahola; Eleonora Lamantea; Holger Prokisch; Hanns Lochmüller; Robert McFarland; V Ramesh; Thomas Klopstock; Peter Freisinger; Fabrizio Salvi; Johannes A Mayr; René Santer; Marketa Tesarova; Jirí Zeman; Bjarne Udd; Robert W Taylor; Douglass Turnbull; Michael Hanna; Doreen Fialho; Anu Suomalainen; Massimo Zeviani; Patrick F Chinnery
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.
Brain : a journal of neurology 2006;129(Pt 7):1674-84.
2006: Angelo Antonini; Stefano Goldwurm; Riccardo Benti; Holger Prokisch; Monika Ebhardt; Roberto Cilia; Michela Zini; Andrea Righini; Giovanni Cossu; Gianni Pezzoli
Genetic, clinical, and imaging characterization of one patient with late-onset, slowly progressive, pantothenate kinase-associated neurodegeneration.
Movement disorders : official journal of the Movement Disorder Society 2006;21(3):417-8.
2006: Monika B Hartig; Konstanze Hörtnagel; Barbara Garavaglia; Giovanna Zorzi; Tomasz Kmiec; Thomas Klopstock; Kevin Rostasy; Marina Svetel; Vladimir S Kostic; Markus Schuelke; Evelyn Botz; Adolf Weindl; Ivana Novakovic; Nardo Nardocci; Holger Prokisch; Thomas Meitinger
Genotypic and phenotypic spectrum of PANK2 mutations in patients with neurodegeneration with brain iron accumulation.
Annals of neurology 2006;59(2):248-56.
2006: Christian Johannes Gloeckner; Norbert Kinkl; Annette Schumacher; Ralf J Braun; Eric O'Neill; Thomas Meitinger; Walter Kolch; Holger Prokisch; Marius Ueffing
The Parkinson disease causing LRRK2 mutation I2020T is associated with increased kinase activity.
Human molecular genetics 2006;15(2):223-32.
2006: Alexander C Adam; Carsten Bornhövd; Holger Prokisch; Walter Neupert; Kai Hell
The Nfs1 interacting protein Isd11 has an essential role in Fe/S cluster biogenesis in mitochondria.
The EMBO journal 2006;25(1):174-83.
2006: Holger Prokisch; Christophe Andreoli; Uwe Ahting; K Heiss; A Ruepp; Curt Scharfe; Thomas Meitinger
MitoP2: the mitochondrial proteome database--now including mouse data.
Nucleic acids research 2006;34(Database issue):D705-11.
2006: Rita Horváth; Angela Abicht; Elke Holinski-Feder; A Laner; Klaus Gempel; Holger Prokisch; Hanns Lochmüller; Thomas Klopstock; Michaela Jaksch
Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA).
Journal of neurology, neurosurgery, and psychiatry 2006;77(1):74-6.
2006: Simone Schmitt; Holger Prokisch; Tilman Schlunck; David G Camp; Uwe Ahting; Thomas Waizenegger; Curt Scharfe; Thomas Meitinger; Axel imhof; Walter Neupert; Peter J Oefner; Doron Rapaport
Proteome analysis of mitochondrial outer membrane from Neurospora crassa.
Proteomics 2006;6(1):72-80.
2004: Holger Prokisch; Curt Scharfe; David G Camp; wenzhong xiao; Lior David; Christophe Andreoli; Matthew Monroe; Ronald J Moore; Marina A Gritsenko; Christian Kozany; Kim K Hixson; Heather M Mottaz; Hans Zischka; Marius Ueffing; Zelek S Herman; Ronald W Davis; Thomas Meitinger; Peter J Oefner; Richard D Smith; Lars M Steinmetz
Integrative analysis of the mitochondrial proteome in yeast.
PLoS biology 2004;2(6):e160.
2004: Jakob C Mueller; Christophe Andreoli; Holger Prokisch; Thomas Meitinger
Mechanisms for multiple intracellular localization of human mitochondrial proteins.
Mitochondrion 2004;3(6):315-25.
2004: Andreja Vasiljev; Uwe Ahting; Frank E Nargang; Nancy E Go; Shukry J Habib; Christian Kozany; Valérie Panneels; Irmgard Sinning; Holger Prokisch; Walter Neupert; Stephan Nussberger; Doron Rapaport
Reconstituted TOM core complex and Tim9/Tim10 complex of mitochondria are sufficient for translocation of the ADP/ATP carrier across membranes.
Molecular biology of the cell 2004;15(3):1445-58.
2004: Christophe Andreoli; Holger Prokisch; Konstanze Hörtnagel; Jakob C Mueller; Martin Münsterkötter; Curt Scharfe; Thomas Meitinger
MitoP2, an integrated database on mitochondrial proteins in yeast and man.
Nucleic acids research 2004;32(Database issue):D459-62.
2003: Dejana Mokranjac; Stefan A Paschen; Christian Kozany; Holger Prokisch; Suzanne C Hoppins; Frank E Nargang; Walter Neupert; Kai Hell
Tim50, a novel component of the TIM23 preprotein translocase of mitochondria.
The EMBO journal 2003;22(4):816-25.
2003: Martin Sichting; Annette Schell-Steven; Holger Prokisch; Ralf Erdmann; Hanspeter Rottensteiner
Pex7p and Pex20p of Neurospora crassa function together in PTS2-dependent protein import into peroxisomes.
Molecular biology of the cell 2003;14(2):810-21.
2003: Konstanze Hörtnagel; Holger Prokisch; Thomas Meitinger
An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria.
Human molecular genetics 2003;12(3):321-7.
2002: Lars M Steinmetz; Curt Scharfe; Adam M Deutschbauer; Dejana Mokranjac; Zelek S Herman; Ted Jones; Angela M Chu; Guri Giaever; Holger Prokisch; Peter J Oefner; Ronald W Davis
Systematic screen for human disease genes in yeast.
Nature genetics 2002;31(4):400-4.
2002: Benedikt Westermann; Holger Prokisch
Mitochondrial dynamics in filamentous fungi.
Fungal genetics and biology : FG & B 2002;36(2):91-7.
2002: Holger Prokisch; Stephan Nussberger; Benedikt Westermann
Protein import into mitochondria of Neurospora crassa.
Fungal genetics and biology : FG & B 2002;36(2):85-90.
2002: Florian Fuchs; Holger Prokisch; Walter Neupert; Benedikt Westermann
Interaction of mitochondria with microtubules in the filamentous fungus Neurospora crassa.
Journal of cell science 2002;115(Pt 9):1931-7.
2001: C Klanner; Holger Prokisch; T Langer
MAP-1 and IAP-1, two novel AAA proteases with catalytic sites on opposite membrane surfaces in mitochondrial inner membrane of Neurospora crassa.
Molecular biology of the cell 2001;12(9):2858-69.
2000: Holger Prokisch; Walter Neupert; Benedikt Westermann
Role of MMM1 in maintaining mitochondrial morphology in Neurospora crassa.
Molecular biology of the cell 2000;11(9):2961-71.
2000: Curt Scharfe; Paolo Zaccaria; K Hoertnagel; Michaela Jaksch; Thomas Klopstock; M Dembowski; Roland Lill; Holger Prokisch; Klaus-Dieter Gerbitz; Walter Neupert; Hans-Werner Mewes; Thomas Meitinger
MITOP, the mitochondrial proteome database: 2000 update.
Nucleic acids research 2000;28(1):155-8.
1999: Curt Scharfe; Paolo Zaccaria; K Hoertnagel; Michaela Jaksch; Thomas Klopstock; Roland Lill; Holger Prokisch; Klaus-Dieter Gerbitz; Hans-Werner Mewes; Thomas Meitinger
MITOP: database for mitochondria-related proteins, genes and diseases.
Nucleic acids research 1999;27(1):153-5.