FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Ilja Demuth

Research Profile

Chemicals & Drugs

Disorders

Physiology

Co-author Network

Publications

TOP 3
Bastian Salewsky; Detlev Schindler; Maren Schmiester; Martin Digweed; Ilja Demuth
The nuclease hSNM1B/Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP/SLX4.
Harald Krenzlin; Bastian Salewsky; Kathrin Weidele; Petra Wessendorf; Alexander Bürkle; Ilja Demuth; Martin Digweed
DNA damage in Nijmegen Breakage Syndrome cells leads to PARP hyperactivation and increased oxidative stress.
Ilja Demuth; Martin Digweed; Petja S Dimova; Thilo Dörk; Véronique Dutrannoy; Timm O Goecke; Luitgard M Graul-Neumann; Hanna Gregorek; Ursula Gruber-Sedlmayr; Csongor Kiss; Peter Michael Kroisel; Charles Marques Lourenco; Wilson Marques; Heidemarie Neitzel; Marion Nicke; Eva Oláh; Detlev Schindler; Ilka Schulze; Sigrun Sodia; Karl Sperling; Katalin Szakszon; Beáta Bessenyei; Veneta Bojinova; Elcin Bora; Tufan Cankaya; Krystyna H Chrzanowska; Joaquim de Sá; Arpad von Moers; Raymonda Varon
New mutations in the ATM gene and clinical data of 25 AT patients.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Ilja Demuth (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Bastian Salewsky; Detlev Schindler; Maren Schmiester; Martin Digweed; Ilja Demuth
The nuclease hSNM1B/Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP/SLX4.
Human molecular genetics 2012;21(22):4948-56.
2012: Harald Krenzlin; Bastian Salewsky; Kathrin Weidele; Petra Wessendorf; Alexander Bürkle; Ilja Demuth; Martin Digweed
DNA damage in Nijmegen Breakage Syndrome cells leads to PARP hyperactivation and increased oxidative stress.
PLoS genetics 2012;8(3):e1002557.
2011: Ilja Demuth; Martin Digweed; Petja S Dimova; Thilo Dörk; Véronique Dutrannoy; Timm O Goecke; Luitgard M Graul-Neumann; Hanna Gregorek; Ursula Gruber-Sedlmayr; Csongor Kiss; Peter Michael Kroisel; Charles Marques Lourenco; Wilson Marques; Heidemarie Neitzel; Marion Nicke; Eva Oláh; Detlev Schindler; Ilka Schulze; Sigrun Sodia; Karl Sperling; Katalin Szakszon; Beáta Bessenyei; Veneta Bojinova; Elcin Bora; Tufan Cankaya; Krystyna H Chrzanowska; Joaquim de Sá; Arpad von Moers; Raymonda Varon
New mutations in the ATM gene and clinical data of 25 AT patients.
Neurogenetics 2011;12(4):273-82.
2010: Véronique Dutrannoy; Ilja Demuth; Ulrich Baumann; Detlev Schindler; Kateryna Konrat; Heidemarie Neitzel; Gabriele Gillessen-Kaesbach; Janina Radszewski; Susanne Rothe; Mario T Schellenberger; Gudrun Nürnberg; Peter Nürnberg; Keng Wee Teik; Revathy Nallusamy; André Reis; Karl Sperling; Martin Digweed; Raymonda Varon
Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype.
Human mutation 2010;31(9):1059-68.
2009: Marco Anders; Jens Mattow; Martin Digweed; Ilja Demuth
Evidence for hSNM1B/Apollo functioning in the HSP70 mediated DNA damage response.
Cell cycle (Georgetown, Tex.) 2009;8(11):1725-32.
2009: Martin Digweed; Ilja Demuth; Lisa Wiesmüller
DNA repair 2008: Tenth Biennial Meeting of the German Society for Research on DNA Repair.
DNA repair 2009;8(3):424-8.
2009: Anna Melchers; Lars Stöckl; Janina Radszewski; Marco Anders; Harald Krenzlin; Candy Kalischke; Regina Scholz; Andreas Jordan; Grit Nebrich; Joachim Klose; Karl Sperling; Martin Digweed; Ilja Demuth
A systematic proteomic study of irradiated DNA repair deficient Nbn-mice.
PloS one 2009;4(5):e5423.
2008: Ilja Demuth; Paul S Bradshaw; Anika Lindner; Marco Anders; Stefanie Heinrich; Julia Kallenbach; Karin Schmelz; Martin Digweed; M Stephen Meyn; Patrick Concannon
Endogenous hSNM1B/Apollo interacts with TRF2 and stimulates ATM in response to ionizing radiation.
DNA repair 2008;7(8):1192-201.
2008: Nadja Thierfelder; Ilja Demuth; Nadine Burghardt; Karin Schmelz; Karl Sperling; Krystyna H Chrzanowska; Eva Seemanova; Martin Digweed
Extreme variation in apoptosis capacity amongst lymphoid cells of Nijmegen breakage syndrome patients.
European journal of cell biology 2008;87(2):111-21.
2007: Ilja Demuth; Martin Digweed
The clinical manifestation of a defective response to DNA double-strand breaks as exemplified by Nijmegen breakage syndrome.
Oncogene 2007;26(56):7792-8.
2007: Lars Krüger; Ilja Demuth; Heidemarie Neitzel; Raymonda Varon; Karl Sperling; Krystyna H Chrzanowska; Eva Seemanova; Martin Digweed
Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS protein.
Carcinogenesis 2007;28(1):107-11.
2006: Jens Mattow; Ilja Demuth; Gisela Haeselbarth; Peter Jungblut; Joachim Klose
Selenium-binding protein 2, the major hepatic target for acetaminophen, shows sex differences in protein abundance.
Electrophoresis 2006;27(8):1683-91.
2005: Yun-Gui Yang; Zdenko Herceg; Koji Nakanishi; Ilja Demuth; Colette Piccoli; Jocelyne Michelon; Gabriele Hildebrand; Maria Jasin; Martin Digweed; Zhao-Qi Wang
The Fanconi anemia group A protein modulates homologous repair of DNA double-strand breaks in mammalian cells.
Carcinogenesis 2005;26(10):1731-40.
2005: Pierre-Olivier Frappart; Wei-Min Tong; Ilja Demuth; Ivan Radovanovic; Zdenko Herceg; Adriano Aguzzi; Martin Digweed; Zhao-Qi Wang
An essential function for NBS1 in the prevention of ataxia and cerebellar defects.
Nature medicine 2005;11(5):538-44.
2005: Neil V Morgan; Fahmida Essop; Ilja Demuth; T J L de Ravel; Stander Jansen; Marc Tischkowitz; Cathryn M Lewis; Linda Wainwright; Janet Poole; Hans Joenje; Martin Digweed; Amanda Krause; Christopher G Mathew
A common Fanconi anemia mutation in black populations of sub-Saharan Africa.
Blood 2005;105(9):3542-4.
2005: Sven Kracker; Yvonne Bergmann; Ilja Demuth; Pierre-Olivier Frappart; Gabriele Hildebrand; Rainer Christine; Zhao-Qi Wang; Karl Sperling; Martin Digweed; Andreas Radbruch
Nibrin functions in Ig class-switch recombination.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(5):1584-9.
2004: Ilja Demuth; Martin Digweed; Patrick Concannon
Human SNM1B is required for normal cellular response to both DNA interstrand crosslink-inducing agents and ionizing radiation.
Oncogene 2004;23(53):8611-8.
2004: Ilja Demuth; Pierre-Olivier Frappart; Gabriele Hildebrand; Anna Melchers; Stephan Lobitz; Lars Stöckl; Raymonda Varon; Zdenko Herceg; Karl Sperling; Zhao-Qi Wang; Martin Digweed
An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability.
Human molecular genetics 2004;13(20):2385-97.
2003: Paola Maraschio; Emanuela Spadoni; Caterina Tanzarella; Antonio Antoccia; Alessandra di Masi; M Maghnie; Raymonda Varon; Ilja Demuth; Luciano Tiepolo; Cesare Danesino
Genetic heterogeneity for a Nijmegen breakage-like syndrome.
Clinical genetics 2003;63(4):283-90.
2002: Martin Digweed; Ilja Demuth; Susanne Rothe; Regina Scholz; Andreas Jordan; Carsten Grötzinger; Detlev Schindler; Markus Grompe; Karl Sperling
SV40 large T-antigen disturbs the formation of nuclear DNA-repair foci containing MRE11.
Oncogene 2002;21(32):4873-8.
2002: Martin Digweed; Susanne Rothe; Ilja Demuth; Regina Scholz; Detlev Schindler; Markus Stumm; Markus Grompe; Andreas Jordan; Karl Sperling
Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia.
Carcinogenesis 2002;23(7):1121-6.
2000: Ilja Demuth; M Wlodarski; Alex J Tipping; Neil V Morgan; Johan P de Winter; M Thiel; S Gräsl; Detlev Schindler; Alan D D'Andrea; Cigdem Altay; H Kayserili; Adriana Zatterale; Jürgen Kunze; Wolfram Ebell; Christopher G Mathew; Hans Joenje; Karl Sperling; Martin Digweed
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.
European journal of human genetics : EJHG 2000;8(11):861-8.
2000: Johan P de Winter; France Léveillé; Carola G M van Berkel; Martin A Rooimans; Laura van der Weel; Jûrgen Steltenpool; Ilja Demuth; Neil V Morgan; Noa Alon; Lucine Bosnoyan-Collins; J Lightfoot; P A J Leegwater; Quinten Waisfisz; K Komatsu; Fré Arwert; Jan C Pronk; Christopher G Mathew; Martin Digweed; Manuel Buchwald; Hans Joenje
Isolation of a cDNA representing the Fanconi anemia complementation group E gene.
American journal of human genetics 2000;67(5):1306-8.
2000: Monika Wilda; Ilja Demuth; P Concannon; Karl Sperling; Horst Hameister
Expression pattern of the Nijmegen breakage syndrome gene, Nbs1, during murine development.
Human molecular genetics 2000;9(12):1739-44.
1998: Johan P de Winter; Quinten Waisfisz; Martin A Rooimans; Carola G M van Berkel; Lucine Bosnoyan-Collins; Noa Alon; Madeleine Carreau; O Bender; Ilja Demuth; Detlev Schindler; Jan C Pronk; Fré Arwert; Holger Hoehn; Martin Digweed; Manuel Buchwald; Hans Joenje
The Fanconi anaemia group G gene FANCG is identical with XRCC9.
Nature genetics 1998;20(3):281-3.
1998: Ilja Demuth; Martin Digweed
Genomic organization of a potential human DNA-crosslink repair gene, KIAA0086.
Mutation research 1998;409(1):11-6.
1998: Tetsuya Otsuki; Jin Wang; Ilja Demuth; Martin Digweed; Johnson Ming-Yu Liu
Assessment of mitomycin C sensitivity in Fanconi anemia complementation group C gene (Fac) knock-out mouse cells.
International journal of hematology 1998;67(3):243-8.