Detlev Schindler

Detlev Schindler

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Detlev Schindler

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Two truncating variants in FANCC and breast cancer risk.

Authors:
Thilo Dörk Paolo Peterlongo Arto Mannermaa Manjeet K Bolla Qin Wang Joe Dennis Thomas Ahearn Irene L Andrulis Hoda Anton-Culver Volker Arndt Kristan J Aronson Annelie Augustinsson Laura E Beane Freeman Matthias W Beckmann Alicia Beeghly-Fadiel Sabine Behrens Marina Bermisheva Carl Blomqvist Natalia V Bogdanova Stig E Bojesen Hiltrud Brauch Hermann Brenner Barbara Burwinkel Federico Canzian Tsun L Chan Jenny Chang-Claude Stephen J Chanock Ji-Yeob Choi Hans Christiansen Christine L Clarke Fergus J Couch Kamila Czene Mary B Daly Isabel Dos-Santos-Silva Miriam Dwek Diana M Eccles Arif B Ekici Mikael Eriksson D Gareth Evans Peter A Fasching Jonine Figueroa Henrik Flyger Lin Fritschi Marike Gabrielson Manuela Gago-Dominguez Chi Gao Susan M Gapstur Montserrat García-Closas José A García-Sáenz Mia M Gaudet Graham G Giles Mark S Goldberg David E Goldgar Pascal Guénel Lothar Haeberle Christopher A Haiman Niclas Håkansson Per Hall Ute Hamann Mikael Hartman Jan Hauke Alexander Hein Peter Hillemanns Frans B L Hogervorst Maartje J Hooning John L Hopper Tony Howell Dezheng Huo Hidemi Ito Motoki Iwasaki Anna Jakubowska Wolfgang Janni Esther M John Audrey Jung Rudolf Kaaks Daehee Kang Pooja Middha Kapoor Elza Khusnutdinova Sung-Won Kim Cari M Kitahara Stella Koutros Peter Kraft Vessela N Kristensen Ava Kwong Diether Lambrechts Loic Le Marchand Jingmei Li Sara Lindström Martha Linet Wing-Yee Lo Jirong Long Artitaya Lophatananon Jan Lubiński Mehdi Manoochehri Siranoush Manoukian Sara Margolin Elena Martinez Keitaro Matsuo Dimitris Mavroudis Alfons Meindl Usha Menon Roger L Milne Nur Aishah Mohd Taib Kenneth Muir Anna Marie Mulligan Susan L Neuhausen Heli Nevanlinna Patrick Neven William G Newman Kenneth Offit Olufunmilayo I Olopade Andrew F Olshan Janet E Olson Håkan Olsson Sue K Park Tjoung-Won Park-Simon Julian Peto Dijana Plaseska-Karanfilska Esther Pohl-Rescigno Nadege Presneau Brigitte Rack Paolo Radice Muhammad U Rashid Gad Rennert Hedy S Rennert Atocha Romero Matthias Ruebner Emmanouil Saloustros Marjanka K Schmidt Rita K Schmutzler Michael O Schneider Minouk J Schoemaker Christopher Scott Chen-Yang Shen Xiao-Ou Shu Jacques Simard Susan Slager Snezhana Smichkoska Melissa C Southey John J Spinelli Jennifer Stone Harald Surowy Anthony J Swerdlow Rulla M Tamimi William J Tapper Soo H Teo Mary Beth Terry Amanda E Toland Rob A E M Tollenaar Diana Torres Gabriela Torres-Mejía Melissa A Troester Thérèse Truong Shoichiro Tsugane Michael Untch Celine M Vachon Ans M W van den Ouweland Elke M van Veen Joseph Vijai Camilla Wendt Alicja Wolk Jyh-Cherng Yu Wei Zheng Argyrios Ziogas Elad Ziv Alison M Dunning Paul D P Pharoah Detlev Schindler Peter Devilee Douglas F Easton

Sci Rep 2019 Aug 29;9(1):12524. Epub 2019 Aug 29.

Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.

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http://dx.doi.org/10.1038/s41598-019-48804-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6715680PMC
August 2019

Elevated blood levels of Dickkopf-1 are associated with acute infections.

Immun Inflamm Dis 2018 12 20;6(4):428-434. Epub 2018 Jul 20.

Centre Hospitalier de Québec-Université Laval Research Center, Québec, G1V 4G2, Canada.

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http://dx.doi.org/10.1002/iid3.232DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247238PMC
December 2018

Mutational Spectrum of Fanconi Anemia Associated Myeloid Neoplasms.

Klin Padiatr 2017 Nov 13;229(6):329-334. Epub 2017 Nov 13.

Faculty of Medicine, Department of Pediatrics and Adolescent Medicine, University of Freiburg, Freiburg.

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http://dx.doi.org/10.1055/s-0043-117046DOI Listing
November 2017

Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia.

J Clin Invest 2017 Aug 10;127(8):3013-3027. Epub 2017 Jul 10.

Department of Human Genetics, Biozentrum, University of Wurzburg, Wurzburg, Germany.

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http://dx.doi.org/10.1172/JCI92069DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5531404PMC
August 2017

RPA-Mediated Recruitment of the E3 Ligase RFWD3 Is Vital for Interstrand Crosslink Repair and Human Health.

Mol Cell 2017 Jun;66(5):610-621.e4

MRC Protein Phosphorylation and Ubiquitylation Unit, School of Life Sciences, Sir James Black Centre, University of Dundee, Dundee DD1 5EH, Scotland. Electronic address:

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http://dx.doi.org/10.1016/j.molcel.2017.04.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459755PMC
June 2017

Human RAD52 - a novel player in DNA repair in cancer and immunodeficiency.

Haematologica 2017 02 15;102(2):e69-e72. Epub 2016 Dec 15.

Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Center of Child and Adolescent Health, Heinrich-Heine-University, Düsseldorf, Germany.

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http://dx.doi.org/10.3324/haematol.2016.155838DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5286958PMC
February 2017

Loss of CDK5RAP2 affects neural but not non-neural mESC differentiation into cardiomyocytes.

Cell Cycle 2015 ;14(13):2044-57

a Institute of Cell Biology and Neurobiology; Charité - Universitätsmedizin Berlin; Campus Mitte ; Berlin , Germany.

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http://dx.doi.org/10.1080/15384101.2015.1044169DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4613649PMC
April 2016

X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy.

Clin Dysmorphol 2016 Apr;25(2):73-6

aInstitute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Duisburg and Essen bDepartment of Neonatology, Vest Children's Hospital Datteln, University Witten/Herdecke, Datteln cInstitute of Human Genetics, Biozentrum, University of Würzburg, Würzburg dDepartment of Obstetrics and Prenatal Medicine, University Bonn Medical School, Bonn eInstitute of Pathology, Charite - Universitaetsmedizin Berlin, Berlin, Germany.

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http://dx.doi.org/10.1097/MCD.0000000000000111DOI Listing
April 2016

Androgen therapy in Fanconi anemia: A retrospective analysis of 30 years in Germany.

Pediatr Hematol Oncol 2016 Feb 22;33(1):5-12. Epub 2016 Feb 22.

f Department of Pediatric Oncology, Hematology, and Stem Cell Transplantation , Charité University Medicine Berlin , Berlin , Germany.

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http://dx.doi.org/10.3109/08880018.2015.1129567DOI Listing
February 2016

FANCJ suppresses microsatellite instability and lymphomagenesis independent of the Fanconi anemia pathway.

Genes Dev 2015 Dec 4;29(24):2532-46. Epub 2015 Dec 4.

DNA Damage Response Laboratory, Clare Hall Laboratories, The Francis Crick Institute, South Mimms EN6 3LD, United Kingdom;

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http://dx.doi.org/10.1101/gad.272740.115DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4699383PMC
December 2015

Immune Thrombocytopenia in Two Unrelated Fanconi Anemia Patients - A Mere Coincidence?

Front Pediatr 2015 8;3:50. Epub 2015 Jun 8.

Division of Pediatric Hematology/Oncology, Department of Pediatrics and Adolescent Medicine, Medical University Graz , Graz , Austria.

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http://dx.doi.org/10.3389/fped.2015.00050DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459098PMC
June 2015

Pollicization of the index finger in Fanconi anaemia: appearances and functionality 40 years after the intervention.

Br J Haematol 2014 Sep 3;166(6):807. Epub 2014 Jul 3.

Department of Imaging Science, University of Manchester, Manchester, UK; Manchester Academic Health Science Centre, Manchester, UK.

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http://doi.wiley.com/10.1111/bjh.12996
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http://dx.doi.org/10.1111/bjh.12996DOI Listing
September 2014

RAG1 deficiency with a shifting B cell phenotype and chromosomal instability.

Clin Immunol 2014 May-Jun;152(1-2):65-7. Epub 2014 Feb 26.

Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Center of Child and Adolescent Health, Heinrich-Heine-University, 40225 Düsseldorf, Germany.

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http://dx.doi.org/10.1016/j.clim.2014.02.009DOI Listing
July 2014

Distinct functional roles for the two SLX4 ubiquitin-binding UBZ domains mutated in Fanconi anemia.

J Cell Sci 2014 Jul 2;127(Pt 13):2811-7. Epub 2014 May 2.

MRC Protein Phosphorylation and Ubiquitylation Unit, College of Life Sciences, Sir James Black Centre, University of Dundee, Dundee DD1 5EH, UK

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http://dx.doi.org/10.1242/jcs.146167DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075355PMC
July 2014

Protective role of RAD50 on chromatin bridges during abnormal cytokinesis.

FASEB J 2014 Mar 16;28(3):1331-41. Epub 2013 Dec 16.

1Hannover Medical School, Gynaecology Research Unit (OE 6411), Carl-Neuberg-Str. 1, D-30625 Hannover, Germany.

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http://dx.doi.org/10.1096/fj.13-236984DOI Listing
March 2014

Visualization of local DNA unwinding by Mre11/Rad50/Nbs1 using single-molecule FRET.

Proc Natl Acad Sci U S A 2013 Nov 4;110(47):18868-73. Epub 2013 Nov 4.

Department of Chemistry and Biochemistry, Department of Molecular Genetics and Microbiology, Institute for Cellular and Molecular Biology, and Howard Hughes Medical Institute, University of Texas, Austin, TX 78712.

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http://dx.doi.org/10.1073/pnas.1309816110DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3839711PMC
November 2013

Abnormal centrosome and spindle morphology in a patient with autosomal recessive primary microcephaly type 2 due to compound heterozygous WDR62 gene mutation.

Orphanet J Rare Dis 2013 Nov 14;8:178. Epub 2013 Nov 14.

Institute of Cell Biology and Neurobiology, Charité University Medicine Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, Berlin 13353, Germany.

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http://dx.doi.org/10.1186/1750-1172-8-178DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225825PMC
November 2013

Acute myeloid leukaemia after treatment for acute lymphoblastic leukaemia in girl with Bloom syndrome.

J Genet Syndr Gene Ther 2013 Sep;4(8)

Stem Cell and Leukaemia Proteomics Laboratory; School of Cancer and Imaging Sciences, The University of Manchester, Manchester Academic Health Science Centre ; Department of Paediatric Onclogy, Royal Manchester Children's Hospital ; Paediatric and Adolescent Oncology, The Christie NHS Foundation Trust, Manchester, UK.

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http://dx.doi.org/10.4172/2157-7412.1000177DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052885PMC
September 2013

Fanconi anemia proteins interact with CtBP1 and modulate the expression of the Wnt antagonist Dickkopf-1.

Blood 2013 Mar 9;121(10):1729-39. Epub 2013 Jan 9.

Centre hospitalier universitaire de Québec Research Center, Québec, QC, Canada.

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http://dx.doi.org/10.1182/blood-2012-02-408997DOI Listing
March 2013

Whole exome sequencing reveals uncommon mutations in the recently identified Fanconi anemia gene SLX4/FANCP.

Hum Mutat 2013 Jan 16;34(1):93-6. Epub 2012 Oct 16.

Department of Human Genetics, University of Wuerzburg, Wuerzburg, Germany.

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http://dx.doi.org/10.1002/humu.22221DOI Listing
January 2013

The nuclease hSNM1B/Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP/SLX4.

Hum Mol Genet 2012 Nov 19;21(22):4948-56. Epub 2012 Aug 19.

Institute of Medical and Human Genetics, Charité-Universitätsmedizin Berlin, Augustenburger Platz 1, Berlin, Germany.

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http://dx.doi.org/10.1093/hmg/dds338DOI Listing
November 2012

Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families.

Hum Mol Genet 2012 Jul 26;21(13):2889-98. Epub 2012 Mar 26.

Human Genetics Group, Human Cancer Genetics Programme, Human Cancer Genetics Programme, Spanish National Cancer Research Centre, C/Melchor Fernández Almagro 3, Madrid, Spain.

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https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
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http://dx.doi.org/10.1093/hmg/dds115DOI Listing
July 2012

On the role of FAN1 in Fanconi anemia.

Blood 2012 Jul 18;120(1):86-9. Epub 2012 May 18.

Genome Instability and DNA Repair Group, Department of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.

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http://dx.doi.org/10.1182/blood-2012-04-420604DOI Listing
July 2012

Analysis of SLX4/FANCP in non-BRCA1/2-mutated breast cancer families.

BMC Cancer 2012 Mar 8;12:84. Epub 2012 Mar 8.

Hereditary Cancer Program, Catalan Institute of Oncology (ICO), Hospital Duran i Reynals, Bellvitge Institute for Biomedical Research (IDIBELL), L'Hospitalet, Barcelona, Catalonia, Spain.

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http://dx.doi.org/10.1186/1471-2407-12-84DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3315397PMC
March 2012

Treatment of the bone marrow failure in Fanconi anemia patients with danazol.

Blood Cells Mol Dis 2012 Feb 16;48(2):128-31. Epub 2011 Dec 16.

Otorhinolaryngology (HNO), Heinrich Heine University, Düsseldorf, Germany.

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http://dx.doi.org/10.1016/j.bcmd.2011.11.006DOI Listing
February 2012

A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region 19q12.

Eur J Med Genet 2012 Jan 27;55(1):49-55. Epub 2011 Aug 27.

Institut für Humangenetik, Universitätsmedizin der Johannes Gutenberg-Universität Mainz, Mainz, Germany.

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http://dx.doi.org/10.1016/j.ejmg.2011.08.001DOI Listing
January 2012

Mutation analysis of the SLX4/FANCP gene in hereditary breast cancer.

Breast Cancer Res Treat 2011 Dec 31;130(3):1021-8. Epub 2011 Jul 31.

Clinics of Obstetrics and Gynaecology, Hannover Medical School, Carl-Neuberg Str. 1, 30625 Hannover, Germany.

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http://dx.doi.org/10.1007/s10549-011-1681-1DOI Listing
December 2011

Fanconi anemia core complex gene promoters harbor conserved transcription regulatory elements.

PLoS One 2011 3;6(8):e22911. Epub 2011 Aug 3.

Department of Human Genetics, University of Wurzburg, Wurzburg, Germany.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0022911PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3149625PMC
December 2011

MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin II.

J Cell Biol 2011 Sep 12;194(6):841-54. Epub 2011 Sep 12.

Chromosome Dynamics Laboratory, RIKEN Advanced Science Institute, Wako, Saitama 351-0198, Japan.

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http://dx.doi.org/10.1083/jcb.201106141DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207293PMC
September 2011

Hepatoblastoma in a 4-year-old girl with Fanconi anaemia.

Acta Paediatr 2011 May 12;100(5):780-3. Epub 2011 Jan 12.

Department of Pediatrics, University Hospital Salzburg, Austria.

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http://dx.doi.org/10.1111/j.1651-2227.2010.02116.xDOI Listing
May 2011

Exploring the link between MORF4L1 and risk of breast cancer.

Authors:
Griselda Martrat Christopher M Maxwell Emiko Tominaga Montserrat Porta-de-la-Riva Núria Bonifaci Laia Gómez-Baldó Massimo Bogliolo Conxi Lázaro Ignacio Blanco Joan Brunet Helena Aguilar Juana Fernández-Rodríguez Sheila Seal Anthony Renwick Nazneen Rahman Julia Kühl Kornelia Neveling Detlev Schindler María J Ramírez María Castellà Gonzalo Hernández Douglas F Easton Susan Peock Margaret Cook Clare T Oliver Debra Frost Radka Platte D Gareth Evans Fiona Lalloo Rosalind Eeles Louise Izatt Carol Chu Rosemarie Davidson Kai-Ren Ong Jackie Cook Fiona Douglas Shirley Hodgson Carole Brewer Patrick J Morrison Mary Porteous Paolo Peterlongo Siranoush Manoukian Bernard Peissel Daniela Zaffaroni Gaia Roversi Monica Barile Alessandra Viel Barbara Pasini Laura Ottini Anna Laura Putignano Antonella Savarese Loris Bernard Paolo Radice Sue Healey Amanda Spurdle Xiaoqing Chen Jonathan Beesley Matti A Rookus Senno Verhoef Madeleine A Tilanus-Linthorst Maaike P Vreeswijk Christi J Asperen Danielle Bodmer Margreet G E M Ausems Theo A van Os Marinus J Blok Hanne E J Meijers-Heijboer Frans B L Hogervorst David E Goldgar Saundra Buys Esther M John Alexander Miron Melissa Southey Mary B Daly Katja Harbst Ake Borg Johanna Rantala Gisela Barbany-Bustinza Hans Ehrencrona Marie Stenmark-Askmalm Bella Kaufman Yael Laitman Roni Milgrom Eitan Friedman Susan M Domchek Katherine L Nathanson Timothy R Rebbeck Oskar Thor Johannsson Fergus J Couch Xianshu Wang Zachary Fredericksen Daniel Cuadras Víctor Moreno Friederike K Pientka Reinhard Depping Trinidad Caldés Ana Osorio Javier Benítez Juan Bueren Tuomas Heikkinen Heli Nevanlinna Ute Hamann Diana Torres Maria Adelaide Caligo Andrew K Godwin Evgeny N Imyanitov Ramunas Janavicius Olga M Sinilnikova Dominique Stoppa-Lyonnet Sylvie Mazoyer Carole Verny-Pierre Laurent Castera Antoine de Pauw Yves-Jean Bignon Nancy Uhrhammer Jean-Philippe Peyrat Philippe Vennin Sandra Fert Ferrer Marie-Agnès Collonge-Rame Isabelle Mortemousque Lesley McGuffog Georgia Chenevix-Trench Olivia M Pereira-Smith Antonis C Antoniou Julián Cerón Kaoru Tominaga Jordi Surrallés Miguel Angel Pujana

Breast Cancer Res 2011 Apr 5;13(2):R40. Epub 2011 Apr 5.

Translational Research Laboratory, Catalan Institute of Oncology, Bellvitge Institute for Biomedical Research (IDIBELL), Gran Via 199, L'Hospitalet del Llobregat 08908, Spain.

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http://dx.doi.org/10.1186/bcr2862DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3219203PMC
April 2011

Genotype-phenotype correlations in Fanconi anemia.

Mutat Res 2009 Jul 21;668(1-2):73-91. Epub 2009 May 21.

Department of Human and Medical Genetics, University of Wurzburg, Biozentrum, Am Hubland, Wurzburg D-97074, Germany.

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http://dx.doi.org/10.1016/j.mrfmmm.2009.05.006DOI Listing
July 2009

Decreased platelet reactivity identified by whole blood flow cytometry in Fanconi anaemia patients.

Thromb Haemost 2007 Dec;98(6):1291-7

University Children's Hospital, University of Wuerzburg, Germany.

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December 2007

Inhibition of primordial germ cell proliferation by the medaka male determining gene Dmrt I bY.

BMC Dev Biol 2007 Aug 30;7:99. Epub 2007 Aug 30.

University of Wurzburg, Physiological Chemistry I, Biozentrum, Am Hubland, D-97074 Wurzburg, Germany.

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http://dx.doi.org/10.1186/1471-213X-7-99DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034567PMC
August 2007

Histone H2AX and Fanconi anemia FANCD2 function in the same pathway to maintain chromosome stability.

EMBO J 2007 Mar 15;26(5):1340-51. Epub 2007 Feb 15.

Group of Mutagenesis, Department of Genetics and Microbiology, Universitat Autònoma de Barcelona, Bellaterra, Barcelona, Spain.

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http://dx.doi.org/10.1038/sj.emboj.7601574DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1817623PMC
March 2007

Fanconi anaemia - response to Manoharan.

Br J Haematol 2006 Oct 22;135(1):139-40. Epub 2006 Aug 22.

Department of Paediatric Oncology, Heinrich Heine University, Duesseldorf, Germany.

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http://dx.doi.org/10.1111/j.1365-2141.2006.06263.xDOI Listing
October 2006

Exclusion/confirmation of ataxia-telangiectasia via cell-cycle testing.

Eur J Pediatr 2006 Apr 13;165(4):250-7. Epub 2006 Jan 13.

Department of Human Genetics, University of Würzburg, Biozentrum am Hubland, 97074, Würzburg, Germany.

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http://link.springer.com/10.1007/s00431-005-0037-4
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http://dx.doi.org/10.1007/s00431-005-0037-4DOI Listing
April 2006

Delayed diagnosis and complications of Fanconi anaemia at advanced age--a paradigm.

Br J Haematol 2006 Apr;133(2):188-97

Department of Paediatric Oncology, Haematology and Immunology, Children's Hospital UKD, Heinrich Heine University, Moorenstrasse 5, 40225 Duesseldorf, Germany.

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http://dx.doi.org/10.1111/j.1365-2141.2006.05998.xDOI Listing
April 2006

Misregulated chromosome condensation in MCPH1 primary microcephaly is mediated by condensin II.

Cell Cycle 2006 Feb 1;5(3):322-6. Epub 2006 Feb 1.

Institut für Humangenetik, Charité-Universitätsmedizin Berlin, Berlin, Germany.

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http://dx.doi.org/10.4161/cc.5.3.2412DOI Listing
February 2006

Prenatal exclusion/confirmation of Fanconi anemia via flow cytometry: a pilot study.

Fetal Diagn Ther 2006 ;21(1):118-24

Department of Human Genetics, University of Wurzburg School of Medicine, Wurzburg, Germany.

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http://dx.doi.org/10.1159/000089061DOI Listing
January 2006

A case report of a patient with microcephaly, facial dysmorphism, mitomycin-c-sensitive lymphocytes, and susceptibility to lymphoma.

Cancer Genet Cytogenet 2006 Jan;164(2):168-71

Division of Pediatric Hematology and Oncology, Children's Hospital of Michigan, Detroit, MI, USA.

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http://dx.doi.org/10.1016/j.cancergencyto.2005.07.025DOI Listing
January 2006

A rapid method for retrovirus-mediated identification of complementation groups in Fanconi anemia patients.

Mol Ther 2005 Nov 9;12(5):976-84. Epub 2005 Aug 9.

Division of Experimental Hematology and Fanconi Anemia Comprehensive Care Center, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

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http://dx.doi.org/10.1016/j.ymthe.2005.04.021DOI Listing
November 2005

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.

Nat Genet 2005 Sep 21;37(9):931-3. Epub 2005 Aug 21.

Laboratory for Human Genetics & Hematology, The Rockefeller University, New York, New York, USA.

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http://dx.doi.org/10.1038/ng1624DOI Listing
September 2005

A role for the Fanconi anemia C protein in maintaining the DNA damage-induced G2 checkpoint.

J Biol Chem 2004 Dec 17;279(49):50986-93. Epub 2004 Sep 17.

Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.

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http://dx.doi.org/10.1074/jbc.M407160200DOI Listing
December 2004