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Detlev Schindler

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Massimo Bogliolo; Juan A. Bueren; José A Casado; Johan P de Winter; Burak Derkunt; Nicolaas G J Jaspers; Kerstin Knies; Jordi Minguillón; Roser Pujol; Anja Raams; María J Ramírez; Paula Rio; Orlando D Schärer; Detlev Schindler; Beatrice Schuster; Chantal Stoepker; Yan Su; Rocío Baños; Javier Benítez; Juan P Trujillo; Sheila Zúñiga; Jordi Surrallés
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia.
Caroline C Huard; Georges Lévesque; Detlev Schindler; Cédric S Tremblay; Marie-Chantal Delisle; Kathrin Helsper; Madeleine Carreau
Fanconi anemia proteins interact with CtBP1 and modulate the expression of the Wnt antagonist Dickkopf-1.
Beatrice Schuster; Chantal Stoepker; Eunike Velleuer; Johan P de Winter; Richard Friedl; Birgit Gottwald-Mühlhauser; Kerstin Knies; Detlev Schindler
Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCP.

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2013: Massimo Bogliolo; Juan A. Bueren; José A Casado; Johan P de Winter; Burak Derkunt; Nicolaas G J Jaspers; Kerstin Knies; Jordi Minguillón; Roser Pujol; Anja Raams; María J Ramírez; Paula Rio; Orlando D Schärer; Detlev Schindler; Beatrice Schuster; Chantal Stoepker; Yan Su; Rocío Baños; Javier Benítez; Juan P Trujillo; Sheila Zúñiga; Jordi Surrallés
Mutations in ERCC4, Encoding the DNA-Repair Endonuclease XPF, Cause Fanconi Anemia.
American journal of human genetics 2013;92(5):800-6.
2013: Caroline C Huard; Georges Lévesque; Detlev Schindler; Cédric S Tremblay; Marie-Chantal Delisle; Kathrin Helsper; Madeleine Carreau
Fanconi anemia proteins interact with CtBP1 and modulate the expression of the Wnt antagonist Dickkopf-1.
Blood 2013;121(10):1729-39.
2013: Beatrice Schuster; Chantal Stoepker; Eunike Velleuer; Johan P de Winter; Richard Friedl; Birgit Gottwald-Mühlhauser; Kerstin Knies; Detlev Schindler
Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCP.
Human mutation 2013;34(1):93-6.
2012: Juan P Trujillo; Joris Andrieux; Massimo Bogliolo; Muriel Holder; Leonardo B Mina; Roser Pujol; Detlev Schindler; Beatrice Schuster; Jordi Surrallés
On the role of FAN1 in Fanconi anemia.
Blood 2012;120(1):86-9.
2012: Kathrin Scheckenbach; Wolfram Scheurlen; Detlev Schindler; Bruce Strimling; Judith Filger-Brillinger; Ulrich Göbel; Mary Morgan; Matthias Sandmann; Helmut Hanenberg
Treatment of the bone marrow failure in Fanconi anemia patients with danazol.
Blood cells, molecules & diseases 2012;48(2):128-31.
2012: Kerstin Knies; Martin Rooimans; Najim Ameziane; Thomas Bettecken; Johan P de Winter; Beatrice Schuster; Detlev Schindler
Genotyping of fanconi anemia patients by whole exome sequencing: advantages and challenges.
PloS one 2012;7(12):e52648.
2012: Ioannis Gavvovidis; Helmut Hanenberg; Frank J Kaiser; Heidemarie Neitzel; Josephine Purps; Isabell Rost; Marc Trimborn; Constanze Wiek; Detlev Schindler
A novel MCPH1 isoform complements the defective chromosome condensation of human MCPH1-deficient cells.
PloS one 2012;7(8):e40387.
2011: Rosa Landwehr; Andreas Meyer; Tjoung-Won Park-Simon; Detlev Schindler; Natalia Antonenkova; Natalia V Bogdanova; Michael Bremer; Peter Hillemanns; Johann H Karstens; Thilo Dörk
Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer.
Breast cancer research and treatment 2011;130(3):1021-8.
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.
2011: Daisuke Yamashita; Ioannis Gavvovidis; Heidemarie Neitzel; Takao Ono; Detlev Schindler; Keishi Shintomi; Marc Trimborn; Tatsuya Hirano
MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin II.
The Journal of cell biology 2011;194(6):841-54.
2011: Magtouf Gatei; Nuri Gueven; Burkhard Jakob; Reinhard Kalb; Amanda W Kijas; Olivier J Becherel; Geoff Birrell; Philip Chen; Thilo Dörk; Shazrul Fazry; Ji-Hoon Lee; Yaniv lerenthal; Tanya T Paull; Detlev Schindler; Gisela Taucher-Scholz; Regina Waltes; Martin F Lavin
ATM protein-dependent phosphorylation of Rad50 protein regulates DNA repair and cell cycle control.
The Journal of biological chemistry 2011;286(36):31542-56.
2011: Juan Alberto Marchal; Stefan Mundlos; Andreas Busche; Veronique Esquitino; Ioannis Gavvovidis; Mahdi Ghani; Luitgard Graul-Neumann; Joachim Hecht; Peter Krawitz; Peter Robinson; Detlev Schindler; Karl Sperling; Nadine Sternberg; Marc Trimborn; Tina Winkler; Heidemarie Neitzel
Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly.
Cell cycle (Georgetown, Tex.) 2011;10(17):2967-77.
2011: Chantal Stoepker; Karolina Hain; Beatrice Schuster; Yvonne Hilhorst-Hofstee; Martin A Rooimans; Jûrgen Steltenpool; Anneke B Oostra; Katharina Eirich; Elisabeth T Korthof; A W M Nieuwint; Nicolaas G J Jaspers; Thomas Bettecken; Hans Joenje; Detlev Schindler; John Rouse; Johan P de Winter
SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype.
Nature genetics 2011;43(2):138-41.
2011: Daniel Meier; Detlev Schindler
Fanconi anemia core complex gene promoters harbor conserved transcription regulatory elements.
PloS one 2011;6(8):e22911.
2010: Ioannis Gavvovidis; Charlotte Pöhlmann; Juan Alberto Marchal; Markus Stumm; Daisuke Yamashita; Tatsuya Hirano; Detlev Schindler; Heidemarie Neitzel; Marc Trimborn
MCPH1 patient cells exhibit delayed release from DNA damage-induced G2/M checkpoint arrest.
Cell cycle (Georgetown, Tex.) 2010;9(24):4893-9.
2010: Linda Hartmann; Kornelia Neveling; Stephanie Borkens; Hildegard Schneider; Marcel Freund; Elke Grassman; Stephan Theiss; A Wawer; Stefan Burdach; Arleen D Auerbach; Detlev Schindler; Helmut Hanenberg; Heiner Schaal
Correct mRNA processing at a mutant TT splice donor in FANCC ameliorates the clinical phenotype in patients and is enhanced by delivery of suppressor U1 snRNAs.
American journal of human genetics 2010;87(4):480-93.
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.
2010: Alfons Meindl; Heide Hellebrand; Constanze Wiek; Verena Erven; Barbara Wappenschmidt; Dieter Niederacher; Marcel Freund; Peter Lichtner; Linda Hartmann; Heiner Schaal; Juliane Ramser; Ellen Honisch; Christian Kubisch; Hans E Wichmann; Karin Kast; Helmut Deissler; Christoph Engel; Bertram Müller-Myhsok; Kornelia Neveling; Marion Kiechle; Christopher G Mathew; Detlev Schindler; Rita K Schmutzler; Helmut Hanenberg
Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
Nature genetics 2010;42(5):410-4.
2010: Fiona Vaz; Helmut Hanenberg; Beatrice Schuster; Karen Barker; Constanze Wiek; Verena Erven; Kornelia Neveling; Daniela Endt; Ian Kesterton; Flavia Autore; Franca Fraternali; Marcel Freund; Linda Hartmann; David Grimwade; Roland Roberts; Heiner Schaal; Shehla Mohammed; Nazneen Rahman; Detlev Schindler; Christopher G Mathew
Mutation of the RAD51C gene in a Fanconi anemia-like disorder.
Nature genetics 2010;42(5):406-9.
2010: Marc Trimborn; Mahdi Ghani; Diego J Walther; Monika Dopatka; Véronique Dutrannoy; Andreas Busche; Franziska Meyer; Stefanie Nowak; Jean Nowak; Zabel Claus; Joachim Klose; Veronica Esquitino; Masoud Garshasbi; Andreas W Kuss; Hans-Hilger Ropers; Susanne Mueller; Charlotte Poehlmann; Ioannis Gavvovidis; Detlev Schindler; Karl Sperling; Heidemarie Neitzel
Establishment of a mouse model with misregulated chromosome condensation due to defective Mcph1 function.
PloS one 2010;5(2):e9242.
2009: Kornelia Neveling; Daniela Endt; Holger Hoehn; Detlev Schindler
Genotype-phenotype correlations in Fanconi anemia.
Mutation research 2009;668(1-2):73-91.
2009: Regina Waltes; Reinhard Kalb; Magtouf Gatei; Amanda W Kijas; Markus Stumm; Alexandra Sobeck; Britta Wieland; Raymonda Varon; Yaniv lerenthal; Martin F Lavin; Detlev Schindler; Thilo Dörk
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder.
American journal of human genetics 2009;84(5):605-16.
2008: Holger Hoehn; Kornelia Neveling; Daniela Endt; Ralph Melcher; Detlev Schindler
Neoplasia, ageing, and genetic instability due to defective caretaker genes.
Cellular oncology : the official journal of the International Society for Cellular Oncology 2008;30(5):461-2.
2007: Susanne Holzhauer; Ana-Gabriela Sitaru; Wolfram Ebell; Detlev Schindler; Helmut Hanenberg; Johannes Wirbelauer; Ulrich Walter; Ralf Grossmann
Decreased platelet reactivity identified by whole blood flow cytometry in Fanconi anaemia patients.
Thrombosis and haemostasis 2007;98(6):1291-7.
2007: Marianne Berwick; Jaya M Satagopan; Leah Ben-Porat; Ann Carlson; Katherine Mah; Rashida Henry; Raffaella Diotti; Kelly Milton; Kanan Pujara; Tom Landers; Sat Dev Batish; José Morales; Detlev Schindler; Helmut Hanenberg; Robert Hromas; Orna Levran; Arleen D Auerbach
Genetic heterogeneity among Fanconi anemia heterozygotes and risk of cancer.
Cancer research 2007;67(19):9591-6.
2007: Reinhard Kalb; Kornelia Neveling; Holger Hoehn; Hildegard Schneider; Yvonne Linka; Sat Dev Batish; Curtis Hunt; Marianne Berwick; Elsa Callen; Jordi Surralles; José A Casado; Juan A. Bueren; Angeles Dasi; Jean Soulier; Eliane Gluckman; C Michel Zwaan; Rosalina Spaendonk; Gerard Pals; Johan P de Winter; Hans Joenje; Markus Grompe; Arleen D Auerbach; Helmut Hanenberg; Detlev Schindler
Hypomorphic mutations in the gene encoding a key Fanconi anemia protein, FANCD2, sustain a significant group of FA-D2 patients with severe phenotype.
American journal of human genetics 2007;80(5):895-910.
2007: Chen Ling; Masamichi Ishiai; Abdullah Ali; Annette L Medhurst; Kornelia Neveling; Reinhard Kalb; Zhijiang Yan; Yutong Xue; Anneke B Oostra; Arleen D Auerbach; Maureen Hoatlin; Detlev Schindler; Hans Joenje; Johan P de Winter; Minoru Takata; Amom Ruhikanta Meetei; Weidong Wang
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway.
The EMBO journal 2007;26(8):2104-14.
2007: José Antonio Casado; Elsa Callén; ariana jacome; Paula Río; Maria Castella; Stephan Lobitz; Teresa Ferro; Arturo Muñoz; Julián Sevilla; Angeles Cantalejo; Elena Cela; José Cervera; Jesús Sánchez-Calero; Isabel Badell; Jesús Estella; Angeles Dasí; Teresa Olivé; Juan José Ortega; Antonia Rodriguez-Villa; María Tapia; Antonio Molinés; Luis Madero; Jose C Segovia; Kornelia Neveling; Reinhard Kalb; Detlev Schindler; Helmut Hanenberg; Jordi Surrallés; Juan A. Bueren
A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network.
Journal of medical genetics 2007;44(4):241-9.
2007: Massimo Bogliolo; Alex Lyakhovich; Elsa Callén; Maria Castellà; Enrico Cappelli; María J Ramírez; Amadeu Creus; Ricard Marcos; Reinhard Kalb; Kornelia Neveling; Detlev Schindler; Jordi Surrallés
Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability.
The EMBO journal 2007;26(5):1340-51.
2007: Sarah Reid; Detlev Schindler; Helmut Hanenberg; Karen Barker; Sandra Hanks; Reinhard Kalb; Kornelia Neveling; Patrick Kelly; Sheila Seal; Marcel Freund; Melanie Wurm; Sat Dev Batish; Francis P Lach; Sevgi Yetgin; Heidemarie Neitzel; Hany Ariffin; Marc Tischkowitz; Christopher G Mathew; Arleen D Auerbach; Nazneen Rahman
Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
Nature genetics 2007;39(2):162-4.
2007: Thomas Grunewald; Ulrike Kammerer; C Winkler; Detlev Schindler; Albert Sickmann; Arnd Honig; Elke Butt
Overexpression of LASP-1 mediates migration and proliferation of human ovarian cancer cells and influences zyxin localisation.
British journal of cancer 2007;96(2):296-305.
2007: Kornelia Neveling; Reinhard Kalb; Andrea R Florl; Sabine Herterich; Richard Friedl; Holger Hoehn; Christiane Hader; F H Hartmann; Indrajit Nanda; Claus Steinlein; Michael Schmid; H Tonnies; C D Hurst; M A Knowles; Helmut Hanenberg; W A Schulz; Detlev Schindler
Disruption of the FA/BRCA pathway in bladder cancer.
Cytogenetic and genome research 2007;118(2-4):166-76.
2007: Amaury Herpin; Detlev Schindler; Anita Kraiss; Ute Hornung; Christoph Winkler; Manfred Schartl
Inhibition of primordial germ cell proliferation by the medaka male determining gene Dmrt I bY.
BMC developmental biology 2007;7():99.
2007: Josephine C Dorsman; Marieke Levitus; Davy A P Rockx; Martin A Rooimans; Anneke B Oostra; Anneke Haitjema; Sietske T Bakker; Jûrgen Steltenpool; Dezsö Schuler; Sheila Mohan; Detlev Schindler; Fré Arwert; Gerard Pals; Christopher G Mathew; Quinten Waisfisz; Johan P de Winter; Hans Joenje
Identification of the Fanconi anemia complementation group I gene, FANCI.
Cellular oncology : the official journal of the International Society for Cellular Oncology 2007;29(3):211-8.
2007: Bernd Gruhn; Joerg Seidel; Felix Zintl; Raymonda Varon; Holger Tönnies; Heidemarie Neitzel; Astrid Bechtold; Holger Hoehn; Detlev Schindler
Successful bone marrow transplantation in a patient with DNA ligase IV deficiency and bone marrow failure.
Orphanet journal of rare diseases 2007;2():5.
2006: Helmut Hanenberg; Kirsten Huck; Sonja Gudowius; Ulrich Göbel; Guido Kobbe; Rainer Haas; Reinhard Kalb; Kornelia Neveling; Detlev Schindler
Fanconi anaemia - response to Manoharan.
British journal of haematology 2006;135(1):139-40.
2006: Susann Bürger; Detlev Schindler; Martin Fehn; Bettina Mühl; Hartmut Mahrhofer; Michael Flentje; Holger Hoehn; Eva Seemanová; Cholpon S Djuzenova
Radiation-induced DNA damage and repair in peripheral blood mononuclear cells from Nijmegen breakage syndrome patients and carriers assessed by the Comet assay.
Environmental and molecular mutagenesis 2006;47(4):260-70.
2006: Thomas Grunewald; Ulrike Kammerer; Elfriede Schulze; Detlev Schindler; Arnd Honig; Michael Zimmer; Elke Butt
Silencing of LASP-1 influences zyxin localization, inhibits proliferation and reduces migration in breast cancer cells.
Experimental cell research 2006;312(7):974-82.
2006: Kirsten Huck; Helmut Hanenberg; Sonja Gudowius; Roland Fenk; Reinhard Kalb; Kornelia Neveling; Beate Betz; Dieter Niederacher; Rainer Haas; Ulrich Göbel; Guido Kobbe; Detlev Schindler
Delayed diagnosis and complications of Fanconi anaemia at advanced age--a paradigm.
British journal of haematology 2006;133(2):188-97.
2006: Tilman Heinrich; Carolin Prowald; Richard Friedl; Benni Gottwald; Reinhard Kalb; Kornelia Neveling; Sabine Herterich; Holger Hoehn; Detlev Schindler
Exclusion/confirmation of ataxia-telangiectasia via cell-cycle testing.
European journal of pediatrics 2006;165(4):250-7.
2006: Marc Trimborn; Detlev Schindler; Heidemarie Neitzel; Tatsuya Hirano
Misregulated chromosome condensation in MCPH1 primary microcephaly is mediated by condensin II.
Cell cycle (Georgetown, Tex.) 2006;5(3):322-6.
2006: Astrid Bechtold; Richard Friedl; Reinhard Kalb; Benni Gottwald; Kornelia Neveling; Ioannis Gavvovidis; Sabine Herterich; Detlev Schindler; Holger Hoehn
Prenatal exclusion/confirmation of Fanconi anemia via flow cytometry: a pilot study.
Fetal diagnosis and therapy 2006;21(1):118-24.
2005: Marc Trimborn; Reyk Richter; Nadine Sternberg; Ioannis Gavvovidis; Detlev Schindler; Andrew P Jackson; Eva-Christina Prott; Karl Sperling; Gabriele Gillessen-Kaesbach; Heidemarie Neitzel
The first missense alteration in the MCPH1 gene causes autosomal recessive microcephaly with an extremely mild cellular and clinical phenotype.
Human mutation 2005;26(5):496.
2005: Saurabh Chandra; Orna Levran; Ingrid Jurickova; Chiel Maas; Rick Kapur; Detlev Schindler; Rashida Henry; Kelly Milton; Sat Dev Batish; Jose A Cancelas; Helmut Hanenberg; Arleen D Auerbach; David A Williams
A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patients.
Molecular therapy : the journal of the American Society of Gene Therapy 2005;12(5):976-84.
2005: Orna Levran; Claire Attwooll; Rashida T Henry; Kelly Milton; Kornelia Neveling; Paula Rio; Sat Dev Batish; Reinhard Kalb; Eunike Velleuer; Sandra Barral; Jurg Ott; John H J Petrini; Detlev Schindler; Helmut Hanenberg; Arleen D Auerbach
The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.
Nature genetics 2005;37(9):931-3.
2005: Elsa Callén; José A Casado; Marc Tischkowitz; Juan A. Bueren; Amadeu Creus; Ricard Marcos; Angeles Dasí; Jesús Estella; Arturo Muñoz; Juan J Ortega; Johan P de Winter; Hans Joenje; Detlev Schindler; Helmut Hanenberg; Shirley V Hodgson; Christopher G Mathew; Jordi Surrallés
A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain.
Blood 2005;105(5):1946-9.
2004: Brian Freie; Samantha L M Ciccone; Xiaxin Li; P Artur Plett; Christie M Orschell; Edward F Srour; Helmut Hanenberg; Detlev Schindler; Suk-Hee Lee; D Wade Clapp
A role for the Fanconi anemia C protein in maintaining the DNA damage-induced G2 checkpoint.
The Journal of biological chemistry 2004;279(49):50986-93.
2004: Reinhard Kalb; Michael Duerr; Matthias Wagner; Sabine Herterich; Michaela Gross; Martin Digweed; Hans Joenje; Holger Hoehn; Detlev Schindler
Lack of sensitivity of primary Fanconi's anemia fibroblasts to UV and ionizing radiation.
Radiation research 2004;161(3):318-25.
2003: Marcel Freund; Corinna Asang; Susanne Kammler; Carolin Konermann; Jörg Krummheuer; Marianne Hipp; Imke Meyer; Wolfram Gierling; Stephan Theiss; Thorsten Preuss; Detlev Schindler; Jørgen Kjems; Heiner Schaal
A novel approach to describe a U1 snRNA binding site.
Nucleic acids research 2003;31(23):6963-75.
2003: Michael Bremer; Detlev Schindler; Michaela Gross; Thilo Dörk; Susanne Morlot; Johann H Karstens
Fanconi's anemia and clinical radiosensitivity report on two adult patients with locally advanced solid tumors treated by radiotherapy.
Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al] 2003;179(11):748-53.
2003: H Popp; Reinhard Kalb; Andreas Fischer; Stephan Lobitz; I Kokemohr; Helmut Hanenberg; Detlev Schindler
Screening Fanconi anemia lymphoid cell lines of non-A, C, D2, E, F, G subtypes for defects in BRCA2/FANCD1.
Cytogenetic and genome research 2003;103(1-2):54-7.
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.
2002: Janine Reichenbach; Ralf Schubert; Detlev Schindler; Klaus Müller; Hansjosef Böhles; Stefan Zielen
Elevated oxidative stress in patients with ataxia telangiectasia.
Antioxidants & redox signaling 2002;4(3):465-9.
2002: Heidemarie Neitzel; Luitgard M Neumann; Detlev Schindler; Andreas Wirges; Holger Tönnies; Marc Trimborn; Alice Krebsova; Reyk Richter; Karl Sperling
Premature chromosome condensation in humans associated with microcephaly and mental retardation: a novel autosomal recessive condition.
American journal of human genetics 2002;70(4):1015-22.
2002: M Gross; Helmut Hanenberg; Stephan Lobitz; Richard Friedl; Sabine Herterich; R Dietrich; Bernd Gruhn; Detlev Schindler; Holger Hoehn
Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction.
Cytogenetic and genome research 2002;98(2-3):126-35.
2001: Cholpon S Djuzenova; A Rothfuss; Ulrich Oppitz; G Spelt; Detlev Schindler; Holger Hoehn; Michael Flentje
Response to X-irradiation of Fanconi anemia homozygous and heterozygous cells assessed by the single-cell gel electrophoresis (comet) assay.
Laboratory investigation; a journal of technical methods and pathology 2001;81(2):185-92.
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: Ralph Melcher; R von Golitschek; Claus Steinlein; Detlev Schindler; Heidemarie Neitzel; K Kainer; Michael Schmid; Holger Hoehn
Spectral karyotyping of Werner syndrome fibroblast cultures.
Cytogenetics and cell genetics 2000;91(1-4):180-5.
1999: Ulrich Oppitz; U Bernthaler; Detlev Schindler; Alexandra Sobeck; Holger Hoehn; Matthias Platzer; A Rosenthal; Michael Flentje
Sequence analysis of the ATM gene in 20 patients with RTOG grade 3 or 4 acute and/or late tissue radiation side effects.
International journal of radiation oncology, biology, physics 1999;44(5):981-8.
1999: Cholpon S Djuzenova; Detlev Schindler; Helga Stopper; Holger Hoehn; Michael Flentje; Ulrich Oppitz
Identification of ataxia telangiectasia heterozygotes, a cancer-prone population, using the single-cell gel electrophoresis (Comet) assay.
Laboratory investigation; a journal of technical methods and pathology 1999;79(6):699-705.
1999: N Sandoval; Matthias Platzer; André Rosenthal; Thilo Dörk; Regina Bendix; Britta Skawran; Manfred Stuhrmann; Rolf-Dieter Wegner; Karl Sperling; S Banin; Yosef Shiloh; A Baumer; U Bernthaler; H Sennefelder; M Brohm; Bernhard H F Weber; Detlev Schindler
Characterization of ATM gene mutations in 66 ataxia telangiectasia families.
Human molecular genetics 1999;8(1):69-79.
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: Kathrin Saar; Detlev Schindler; Rolf-Dieter Wegner; A Reis; Thomas F Wienker; Holger Hoehn; Hans Joenje; Karl Sperling; Martin Digweed
Localisation of a Fanconi anaemia gene to chromosome 9p.
European journal of human genetics : EJHG 1998;6(5):501-8.
1998: Verena Preisler; Helga Stopper; Detlev Schindler; Richard Friedl; Leo Pfreundner; Florian Hoppe; Rudolf Hagen
Cytotoxic and genotoxic effects of paclitaxel (Taxol) and radiation in a squamous cell carcinoma cell line of the larynx.
Acta oto-laryngologica 1998;118(4):600-5.
1997: W Liebetrau; T M Rünge; A Baumer; C Henning; O Gross; Detlev Schindler; Martin Poot; Holger Hoehn
Exploring the role of oxygen in Fanconi's anemia.
Recent results in cancer research. Fortschritte der Krebsforschung. Progrès dans les recherches sur le cancer 1997;143():353-67.
1996: A Baumer; U Bernthaler; W Wolz; Holger Hoehn; Detlev Schindler
New mutations in the ataxia telangiectasia gene.
Human genetics 1996;98(2):246-9.
1995: H Seyschab; R Friedl; Y Sun; Detlev Schindler; Holger Hoehn; S Hentze; T Schroeder-Kurth
Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia.
Blood 1995;85(8):2233-7.
1994: H Seyschab; G Bretzel; R Friedl; Detlev Schindler; Y Sun; Holger Hoehn
Modulation of the spontaneous G2 phase blockage in Fanconi anemia cells by caffeine: differences from cells arrested by X-irradiation.
Mutation research 1994;308(2):149-57.
1993: H Seyschab; Y Sun; R Friedl; Detlev Schindler; Holger Hoehn
G2 phase cell cycle disturbance as a manifestation of genetic cell damage.
Human genetics 1993;92(1):61-8.
1992: H Seyschab; Detlev Schindler; R Friedl; Gotthold Barbi; E Boltshauser; J P Fryns; F Hanefeld; R Korinthenberg; I Krägeloh-Mann; J M J C Scheres
Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromes.
European journal of pediatrics 1992;151(10):756-60.
1991: Gotthold Barbi; J M J C Scheres; Detlev Schindler; R D Taalman; K Rodens; K Mehnert; M Müller; H Seyschab
Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded child.
American journal of medical genetics 1991;40(1):44-50.
1989: H Seyschab; R Friedl; Detlev Schindler; Holger Hoehn; Peter S Rabinovitch; U Chen
The effects of bacterial lipopolysaccharide, anti-receptor antibodies and recombinant interferon on mouse B cell cycle progression using 5-bromo-2'-deoxyuridine/Hoechst 33258 dye flow cytometry.
European journal of immunology 1989;19(9):1605-12.
1989: M Poot; H Schmitt; H Seyschab; J Koehler; U Chen; U Kaempf; M Kubbies; Detlev Schindler; Peter S Rabinovitch; Holger Hoehn
Continuous bromodeoxyuridine labeling and bivariate ethidium bromide/Hoechst flow cytometry in cell kinetics.
Cytometry 1989;10(2):222-6.
1989: Michael Schmid; Thomas Haaf; Detlev Schindler; M Meurer
Centromeric association of a microchromosome. A new category of non-random arrangement of metaphase chromosomes.
Human genetics 1989;81(2):127-36.
1989: Michael Schmid; E Enderle; Detlev Schindler; W Schempp
Chromosome banding and DNA replication patterns in bird karyotypes.
Cytogenetics and cell genetics 1989;52(3-4):139-46.
1988: Detlev Schindler; Holger Hoehn
Fanconi anemia mutation causes cellular susceptibility to ambient oxygen.
American journal of human genetics 1988;43(4):429-35.
1988: Detlev Schindler; M Kubbies; R E Priest; H Hoehn; Peter S Rabinovitch
The phytohemagglutinin response of human peripheral blood lymphocytes as a function of donor age: a re-examination using BrdU-Hoechst flow cytometry.
Mechanisms of ageing and development 1988;44(3):253-63.
1988: M Poot; Detlev Schindler; M Kubbies; Holger Hoehn; Peter S Rabinovitch
Bromodeoxyuridine amplifies the inhibitory effect of oxygen on cell proliferation.
Cytometry 1988;9(4):332-8.
1987: Detlev Schindler; H Seyschab; M Poot; Holger Hoehn; A Schinzel; J P Fryns; Niels Tommerup; Peter S Rabinovitch
Screening test for ataxia telangiectasia.
Lancet 1987;2(8572):1398-9.