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Manfred Fliegauf

Research Profile

Anatomy

Cilium

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Zuzanna Bukowy-Bieryłło; Manfred Fliegauf; Maciej Geremek; Eric Haan; Niki Tomas Loges; James Martin; Lucy Morgan; Heike Olbrich; Heymut Omran; Andrzej Pogorzelski; Ewa Rutkiewicz; Jonathan Rutland; Katarzyna Voelkel; Mariana Wittmer; Ewa Ziętkiewicz; Wolfgang Berger; Michał Witt
RPGR mutations might cause reduced orientation of respiratory cilia.
Manfred Fliegauf; Bernhard Kremer; Andreas F-P Sonnen; Philipp Henneke
Mucociliary clearance defects in a murine in vitro model of pneumococcal airway infection.
Björn Hackanson; Manfred Jung; Mahmoud Abdelkarim; Marco Benkißer; Manfred Fliegauf; Leander Rimmele; Michael Lübbert
HDAC6 as a target for antileukemic drugs in acute myeloid leukemia.

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All Publications

2013: Zuzanna Bukowy-Bieryłło; Manfred Fliegauf; Maciej Geremek; Eric Haan; Niki Tomas Loges; James Martin; Lucy Morgan; Heike Olbrich; Heymut Omran; Andrzej Pogorzelski; Ewa Rutkiewicz; Jonathan Rutland; Katarzyna Voelkel; Mariana Wittmer; Ewa Ziętkiewicz; Wolfgang Berger; Michał Witt
RPGR mutations might cause reduced orientation of respiratory cilia.
Pediatric pulmonology 2013;48(4):352-63.
2013: Manfred Fliegauf; Bernhard Kremer; Andreas F-P Sonnen; Philipp Henneke
Mucociliary clearance defects in a murine in vitro model of pneumococcal airway infection.
PloS one 2013;8(3):e59925.
2012: Björn Hackanson; Manfred Jung; Mahmoud Abdelkarim; Marco Benkißer; Manfred Fliegauf; Leander Rimmele; Michael Lübbert
HDAC6 as a target for antileukemic drugs in acute myeloid leukemia.
Leukemia research 2012;36(8):1055-62.
2011: Fabian Schmid; Gudrun Nürnberg; Peter Nürnberg; Heymut Omran; Daniel Barthelmes; Wolfgang Berger; Manfred Fliegauf; Harald Gaspar; Esther Glaus; John Neidhardt
U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutation.
Human mutation 2011;32(7):815-24.
2011: Anita Becker-Heck; Irene E Zohn; Noriko Okabe; Andrew Pollock; Kari Baker Lenhart; Jessica Sullivan-Brown; Jason McSheene; Niki Tomas Loges; Heike Olbrich; Karsten Haeffner; Manfred Fliegauf; Judith Horvath; Richard Reinhardt; Kim G Nielsen; June K Marthin; György Baktai; Kathryn V Anderson; Robert Geisler; Lee Niswander; Heymut Omran; Rebecca D Burdine
The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation.
Nature genetics 2011;43(1):79-84.
2010: Axel Karow; Christian Flotho; Michaela Schneider; Manfred Fliegauf; Charlotte M Niemeyer
Mutations of the Shwachman-Bodian-Diamond syndrome gene in patients presenting with refractory cytopenia--do we have to screen?
Haematologica 2010;95(4):689-90.
2009: Mignon L Loh; Debbie S Sakai; Christian Flotho; Michelle Kang; Manfred Fliegauf; Sophie Archambeault; Charles G Mullighan; Leslie Chen; Eva Bergstraesser; Carlos E Bueso-Ramos; Peter D Emanuel; Henrik Hasle; Jean-Pierre J Issa; Marry M van den Heuvel-Eibrink; Franco Locatelli; Jan Stary; Monika M Trebo; Marcin Wlodarski; Marco Zecca; Kevin Shannon; Charlotte M Niemeyer
Mutations in CBL occur frequently in juvenile myelomonocytic leukemia.
Blood 2009;114(9):1859-63.
2008: Heymut Omran; Daisuke Kobayashi; Heike Olbrich; Tatsuya Tsukahara; Niki Tomas Loges; Haruo Hagiwara; Qi Zhang; Gerard Leblond; Eileen O'Toole; Chikako Hara; Hideaki Mizuno; Hiroyuki Kawano; Manfred Fliegauf; Toshiki Yagi; Sumito Koshida; Atsushi Miyawaki; Hanswalter Zentgraf; Horst Seithe; Richard Reinhardt; Yoshinori Watanabe; Ritsu Kamiya; David R Mitchell; Hiroyuki Takeda
Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneins.
Nature 2008;456(7222):611-6.
2008: Niki Tomas Loges; Heike Olbrich; Lale Fenske; Huda Mussaffi; Judit Horvath; Manfred Fliegauf; Heiner Kuhl; György Baktai; Erzsebet Peterffy; Rahul Chodhari; Eddie M K Chung; Andrew Rutman; Christopher O'Callaghan; Hannah Blau; Laszlo Tiszlavicz; Katarzyna Voelkel; Michal Witt; Ewa Zietkiewicz; Juergen Neesen; Richard Reinhardt; Hannah M Mitchison; Heymut Omran
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein arm.
American journal of human genetics 2008;83(5):547-58.
2008: Tobias Berg; Manfred Fliegauf; Jan Burger; Martin S Staege; Shaohua Liu; Natalia Martinez; Olaf Heidenreich; Stefan Burdach; Torsten Haferlach; Milton H Werner; Michael Lübbert
Transcriptional upregulation of p21/WAF/Cip1 in myeloid leukemic blasts expressing AML1-ETO.
Haematologica 2008;93(11):1728-33.
2008: Carsten Bergmann; Manfred Fliegauf; Nadina Ortiz Brüchle; Valeska Frank; Heike Olbrich; Jan Kirschner; Bernhard Schermer; Ingolf Schmedding; Andreas Kispert; Bettina Kränzlin; Gudrun Nürnberg; Christian Becker; Tiemo Grimm; Gundula Girschick; Sally A Lynch; Peter Kelehan; Jan Senderek; Thomas J Neuhaus; Thomas Stallmach; Hanswalter Zentgraf; Peter Nürnberg; Norbert Gretz; Cecilia Lo; Soeren Lienkamp; Tobias Schäfer; Gerd Walz; Thomas Benzing; Klaus Zerres; Heymut Omran
Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia.
American journal of human genetics 2008;82(4):959-70.
2008: Georg C Schwabe; Katrin Hoffmann; Niki Tomas Loges; Daniel Birker; Colette Rossier; Margherita M de Santi; Heike Olbrich; Manfred Fliegauf; Mike Failly; Uta Liebers; Mirella Collura; Gerhard Gaedicke; Stefan Mundlos; Ulrich Wahn; Jean-Louis Blouin; Bodo Niggemann; Heymut Omran; Stylianos E Antonarakis; Lucia Bartoloni
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations.
Human mutation 2008;29(2):289-98.
2007: Manfred Fliegauf; Thomas Benzing; Heymut Omran
When cilia go bad: cilia defects and ciliopathies.
Nature reviews. Molecular cell biology 2007;8(11):880-93.
2007: Christian von Schnakenburg; Manfred Fliegauf; Heymut Omran
Nephrocystin and ciliary defects not only in the kidney?
Pediatric nephrology (Berlin, Germany) 2007;22(6):765-9.
2007: Tobias Berg; Yalin Guo; Mahmoud Abdelkarim; Manfred Fliegauf; Michael Lübbert
Reversal of p15/INK4b hypermethylation in AML1/ETO-positive and -negative myeloid leukemia cell lines.
Leukemia research 2007;31(4):497-506.
2006: Rainer Claus; Manfred Fliegauf; Michael Stock; Jesús A Duque; Mateusz Kolanczyk; Michael Lübbert
Inhibitors of DNA methylation and histone deacetylation independently relieve AML1/ETO-mediated lysozyme repression.
Journal of leukocyte biology 2006;80(6):1462-72.
2006: Bernhard Schermer; Cristina Ghenoiu; Malte Bartram; Roman Ulrich Müller; Fruzsina Kotsis; Martin Höhne; Wolfgang Kühn; Manuela Rapka; Roland Nitschke; Hanswalter Zentgraf; Manfred Fliegauf; Heymut Omran; Gerd Walz; Thomas Benzing
The von Hippel-Lindau tumor suppressor protein controls ciliogenesis by orienting microtubule growth.
The Journal of cell biology 2006;175(4):547-54.
2006: Manfred Fliegauf; Judit Horvath; Christian von Schnakenburg; Heike Olbrich; Dominik Müller; Julia Thumfart; Bernhard Schermer; Gregory Pazour; Hartmut P H Neumann; Hanswalter Zentgraf; Thomas Benzing; Heymut Omran
Nephrocystin specifically localizes to the transition zone of renal and respiratory cilia and photoreceptor connecting cilia.
Journal of the American Society of Nephrology : JASN 2006;17(9):2424-33.
2006: Bartlomiej Budny; Wei Chen; Heymut Omran; Manfred Fliegauf; Andreas Tzschach; Marzena Wisniewska; Lars Riff Jensen; Martine Raynaud; Sarah A Shoichet; Magda Badura; Steffen Lenzner; Anna Latos-Bielenska; Hans-Hilger Ropers
A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral-facial-digital type I syndrome.
Human genetics 2006;120(2):171-8.
2006: Nada Hornef; Heike Olbrich; Judit Horvath; Maimoona A Zariwala; Manfred Fliegauf; Niki Tomas Loges; Johannes H Wildhaber; Peadar G Noone; Marcus Kennedy; Stylianos E Antonarakis; Jean-Louis Blouin; Lucia Bartoloni; Thomas Nüsslein; Peter Ahrens; Matthias Griese; Heiner Kuhl; Ralf Sudbrak; Michael Knowles; Richard Reinhardt; Heymut Omran
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects.
American journal of respiratory and critical care medicine 2006;174(2):120-6.
2006: Y Lu; Ya-Bei Xu; T-T Yuan; M-G Song; Michael Lübbert; Manfred Fliegauf; Guo-Qiang Chen
Inducible expression of AML1-ETO fusion protein endows leukemic cells with susceptibility to extrinsic and intrinsic apoptosis.
Leukemia 2006;20(6):987-93.
2006: Manfred Fliegauf; Heymut Omran
Novel tools to unravel molecular mechanisms in cilia-related disorders.
Trends in genetics : TIG 2006;22(5):241-5.
2006: Jörn Lausen; Shaohua Liu; Manfred Fliegauf; Michael Lübbert; Milton H Werner
ELA2 is regulated by hematopoietic transcription factors, but not repressed by AML1-ETO.
Oncogene 2006;25(9):1349-57.
2006: Jorn Oliver Sass; Verena Mohr; Heike Olbrich; Udo Engelke; Judit Horvath; Manfred Fliegauf; Niki Tomas Loges; Susanne Schweitzer-Krantz; Ralf Moebus; Polly Weiler; Andreas Kispert; andrea superti-furga; Ron A Wevers; Heymut Omran
Mutations in ACY1, the gene encoding aminoacylase 1, cause a novel inborn error of metabolism.
American journal of human genetics 2006;78(3):401-9.
2005: Bernhard Schermer; Katja Höpker; Heymut Omran; Cristina Ghenoiu; Manfred Fliegauf; Andrea Fekete; Judit Horvath; Michael Köttgen; Matthias Hackl; Stefan Zschiedrich; Tobias B Huber; Albrecht Kramer-Zucker; Hanswalter Zentgraf; Andree Blaukat; Gerd Walz; Thomas Benzing
Phosphorylation by casein kinase 2 induces PACS-1 binding of nephrocystin and targeting to cilia.
The EMBO journal 2005;24(24):4415-24.
2005: Judit Horváth; Manfred Fliegauf; Heike Olbrich; Andreas Kispert; Stephen M King; Hannah M Mitchison; Maimoona A Zariwala; Michael Knowles; Ralf Sudbrak; György Fekete; Juergen Neesen; Richard Reinhardt; Heymut Omran
Identification and analysis of axonemal dynein light chain 1 in primary ciliary dyskinesia patients.
American journal of respiratory cell and molecular biology 2005;33(1):41-7.
2005: Manfred Fliegauf; Heike Olbrich; Judit Horvath; Johannes H Wildhaber; Maimoona A Zariwala; Marcus Kennedy; Michael Knowles; Heymut Omran
Mislocalization of DNAH5 and DNAH9 in respiratory cells from patients with primary ciliary dyskinesia.
American journal of respiratory and critical care medicine 2005;171(12):1343-9.
2004: Manfred Fliegauf; Michael Stock; Tobias Berg; Michael Lübbert
Williams-Beuren syndrome critical region-5/non-T-cell activation linker: a novel target gene of AML1/ETO.
Oncogene 2004;23(56):9070-81.
2004: Inés Ibañez-Tallon; Axel Pagenstecher; Manfred Fliegauf; Heike Olbrich; Andreas Kispert; Uwe-Peter Ketelsen; Alison North; Nathaniel Heintz; Heymut Omran
Dysfunction of axonemal dynein heavy chain Mdnah5 inhibits ependymal flow and reveals a novel mechanism for hydrocephalus formation.
Human molecular genetics 2004;13(18):2133-41.
2004: Michael Stock; Henning Schäfer; Manfred Fliegauf; Florian Otto
Identification of novel genes of the bone-specific transcription factor Runx2.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2004;19(6):959-72.
2003: Florian Otto; Michael Stock; Manfred Fliegauf; P Fenaux; C Preudhomme; Michael Lübbert
Absence of somatic mutations within the Runt domain of AML2/RUNX3 in acute myeloid leukaemia.
Leukemia 2003;17(8):1677-8.
2003: Heike Olbrich; Manfred Fliegauf; Julia Hoefele; Andreas Kispert; Edgar Otto; Andreas Volz; Matthias T F Wolf; Gürsel Sasmaz; Ute Trauer; Richard Reinhardt; Ralf Sudbrak; Corinne Antignac; Norbert Gretz; Gerd Walz; Bernhard Schermer; Thomas Benzing; Friedhelm Hildebrandt; Heymut Omran
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.
Nature genetics 2003;34(4):455-9.
2003: Manfred Fliegauf; Christian Fröhlich; Judit Horvath; Heike Olbrich; Friedhelm Hildebrandt; Heymut Omran
Identification of the human CYS1 gene and candidate gene analysis in Boichis disease.
Pediatric nephrology (Berlin, Germany) 2003;18(6):498-505.
2002: Ditsa Levanon; David Bettoun; Catherine Harris-Cerruti; Eilon Woolf; Varda Negreanu; Raya Eilam; Yael Bernstein; Dalia Goldenberg; Cuiying Xiao; Manfred Fliegauf; Eitan Kremer; Florian Otto; Ori Brenner; Aharon Lev-Tov; Yoram Groner
The Runx3 transcription factor regulates development and survival of TrkC dorsal root ganglia neurons.
The EMBO journal 2002;21(13):3454-63.
2002: Jan Henrik Eggers; Michael Stock; Manfred Fliegauf; Birgitta Vonderstrass; Florian Otto
Genomic characterization of the RUNX2 gene of Fugu rubripes.
Gene 2002;291(1-2):159-67.