Fanconi Anemia Scientific Symposium Poster Presentations
September 29th - October 2 , Geneva, Switzerland
Alter, Blanche P. National Cancer Institute, Rockville, MDCancer as the Initial Presentation in Patients with Fanconi’s Anemia
Alter, Blanche P.National Cancer Institute, Rockville, MD Fanconi’s Anemia Due to Mutations in FANCD1/BRCA2: Cancer Risk, Phenotype, and Prospective Follow-up
Ameziane, Najim Vrije University Medical Center, Amsterdam, The Netherlands Absence of Genetic and Epigenetic Aberrations in Fanconi Anemia Genes in Pediatric Non-FA Acute Myeloid Leukemia
Ameziane, Najim Vrije University Medical Center, Amsterdam, The Netherlands Comprehensive Mutation Screening for Fanconi Anemia
Andreassen, Paul R.Cincinnati Children’s Hospital Medical Center, Cincinnati, OHMonoubiquitinated FANCD2 Recruits the Machinery for Homologous Recombination to the Replication Fork: Implications for the Etiology of Fanconi Anemia
Baker, JillianThe Hospital for Sick Children, Toronto, Ontario Allogeneic Hematopoietic Stem Cell Transplantation of Patients with Fanconi Anemia and High Risk Features Using Fludarabine without Radiation
Briot, DelphineGustave Roussy Institute, Villejuif, France MMP-7 Overexpression Leads to TNF-alpha Overproduction in Fanconi Anemia
Bueren, Juan A.CIEMAT, Madrid, Spain A Simplified Approach to Improve the Efficiency and Safety of Ex Vivo Hematopoietic Gene Therapy in Fanconi Anemia Patients
Bueren, Juan A.CIEMAT, Madrid, SpainSevere Hematopoietic Stem Cell Defects in Mice with a Hypomorphic Mutation in Brca2
Calzone, RitaElena D'Aosta Hospital, Naples, ItalyCytological Aspects Leading to New Interpretations in Fanconi Anemia Cellular Biology
Camboni, Maria GavinaInstitute of Biomolecular Chemistry, Sassari, ItalyExpression Analysis of FANCG and FANCC Genes in Sporadic Colon Cancer
Camelo, Ricardo MesquitaInstitute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, BrazilAmifostine Protection against Mitomycin-induced Chromosomal Breakage in Fanconi Anaemia Lymphocytes
Cantor, Sharon B.University of Massachusetts Cancer Center, Worcester, MABACH1 is Critical for Homologous Recombination and Appears to be the Fanconi Anemia Gene Product FANCJ
Chuang, Alice Y. C.Johns Hopkins Medical Institution, Baltimore, MDp53 Inactivation Results in Chromosomal Instability and the Presence of Telomere DNA in Interphase Bridges
Chuang, TonyJohns Hopkins Medical Institution, Baltimore, MDThree Dimensional Organization of Telomeres in Head and Neck Cancer
Collis, SpencerThe London Research Institute, Clare Hall Laboratories, South Mimms, United KingdomFunctional Analysis of the C. elegans FANCD2 Homologue
Constantinou, AngelosUniversity of Lausanne, Epalinges, SwitzerlandDefining the Connections between FA Proteins, DNA Replication and DNA Lesions
de Vries, Yne WaterhamVrije University Medical Center, Amsterdam, The NetherlandsEvidence for a New Complementation Group with a Defect Downstream in the Fanconi Anemia Pathway
Dufour, CarloG. Gaslini Children’s Hospital, Genoa, ItalyRole of TRAIL in the Induction of Apoptosis in Fanconi Anemia Cell Line A
Gallego, Marta Susana

Garrahan Pediatric's Hospital, Buenos Aires, Argentina

Distinctive Clinical Features in Patients with Presumptive Diagnosis of Fanconi Anemia in a Single Institution in Argentina
Gangopadhyay, NupurUniversity of Pittsburgh, Pittsburgh, PANotch Ligand (Delta-like-1) Can Support the Development of Bone Marrow Stem Cells
Gluckman, Eliane Hôpital Saint-Louis, Paris, FrancePotentials and Limits of Gene Therapy in Fanconi Anemia
Gökçora, I. HalukCebeci Hospital, Dikimevi, Ankara, TurkeyA Case of Fanconi’s Anemia with an Initial Presentation of Abdominal Rhabdomyosarcoma
Howlett, Niall G.University of Michigan, Ann Arbor, MIThe Fanconi Anemia Pathway is Required for the DNA Replication Stress Response and for the Regulation of Common Fragile Site Stability
Hutchinson, Amy AnnNational Cancer Institute, Gaithersburg, MDSequence Analysis of Common and Rare Variants in the Fanconi Anemia Complementation Group A Gene, FANCA, in Diverse Geo-Ethnic Healthy Populations
Jones, Nigel J.University of Liverpool, UKCharacterisation of a Fancl Chinese Hamster Cell Mutant
Kelly, Patrick F.Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OHCollection and Purification of Fanconi Anemia CD34+ Hematopoietic Stem and Progenitor Cells (HSC) for Future Autologous Use: Initial Clinical Results
Kelly, Patrick F.Cincinnati Children's Hospital Medical Center and the University of Cincinnati College of Medicine, Cincinnati, OHGene Transfer for Patients with Fanconi Anemia, Genotype A: A Pilot Study
Kitao, HiroyukiKawasaki Medical School, Okayama, JapanFunctional Relationship between FANCD1/BRCA2-Rad51 Pathway and the Fanconi Anemia Pathway in DNA Repair
Kluzek, KatarzynaNicolaus Copernicus University, Bydgoszcz, PolandChinese Hamster Cell Mutant CL-V5B is Defective in the Fancc Gene
Krejci, LumirYale University School of Medicine, New Haven, CT Role of BRCA2/FANCD1 in Homologous Recombination
Lambert, Muriel W.UMDNJ—New Jersey Medical School, Newark, NJ Functional Importance of the Interaction of Alpha Spectrin and the FANC Proteins in the Repair of DNA Interstrand Cross-links and the Repair Defect in Fanconi Anemia Cells
Lambert, Muriel W.UMDNJ—New Jersey Medical School, Newark, NJ The Co-Recessive Inheritance Model: A Paradigm for Fanconi Anemia
Lee, Suk-Hee Indiana University School of Medicine, Indianapolis, INFanconi Anemia Group D2 Protein is a Novel Apoptotic Target Mediated by Caspases
Marini, Federica Universita' degli Studi di Milano, Italy Identification of Novel Factors Involved in Interstrand Cross-link Repair
Meyer, Stefan Central Manchester and Manchester Children's University Hospital NHS Trust, Manchester, UKEVI1 Amplification in FA-derived AML Cell Lines with Bi-allelic FANCD1/BRCA2 Mutations
Meyer, StefanCentral Manchester and Manchester Children's University Hospital NHS Trust, Manchester, UKNo Evidence of Significant FANCF Methylation in Sporadic Acute Childhood Leukaemia
Morgese, Fabio Telethon Institute of Genetics and Medicine, Naples ItalyCharacterization of Two Novel Interactors of the Fanconi Anemia Protiens
Mosedale, GeorginaMRC Laboratory of Molecular Biology, Division of Protein and Nucleic Acid Chemistry, Cambridge, UKThe Ku70 Protein Subverts Homologous Recombination Repair Following Inactivation of the Fanconi Anaemia Pathway
Nakanishi, Koji Memorial Sloan-Kettering Cancer Center, New York, NYFA Pathway and Double-strand Break Repair
Navarro, Susana CIEMAT, Madrid, SpainA Fast and Reliable Procedure for the Genotyping Fanconi Anemia Knockout Mice Using Melting Curves Analysis From Multiplex qPCR
Neveling, Kornelia University of Würzburg, GermanyFanconi Anemia Mutation Screen in Bladder Carcinoma.
O'Donnell, Paul Fred Hutchinson Cancer Research Center, Seattle, WANonmyeloablative Hematopoietic Cell Transplantation of Advanced Hematologic Malignancies using Haploidentical Donors
Olsen, AnnaJohn Radcliffe Hospital, Oxford, UKProcesssing of Interstrand Cross-links by Excision Repair Factors: Impact on Activation of the Fanconi Anemia Pathway
Papadopoulo, Dora Institute Curie, Research Division, Paris, FranceFANC Genes and Double Strand Break Repair
Patel, K.J. MRC Laboratory of Molecular Biology, Division of Protein and Nucleic Acid Chemistry, Cambridge, UKThe Power of the Chicken DT40 System in Defining Defective DNA Repair in Fanconi Anaemia
Perrina, Franco MRC Laboratory of Molecular Biology Division of Protein and Nucleic Acid Chemistry, Cambridge, UKProgress Towards a Crystal Structure of FANCD2
Pipaón, Carlos Hospital Universitario Marqués de Valdecilla Edificio Escuela Enfermería, Santander, Spain Defective DNA Binding of Transcriptional Repressor ZEB via Methylation Results in Increased Constitutive Levels of p73 in Fanconi Anemia Cells
Ray, Kallol Harvard Medical School, Boston, MAStructural Studies of FANCE and FANCD2 Proteins
Roomi, M. WaheedMatthias Rath Research Institute, Santa Clara, CADown Regulation of Matrix Metalloproteinases and Inhibition of Cell Invasion by a Novel Nutrient Mixture in Human Fanconi Anemia Fibroblast Cell Lines: In Vitro Study
Rünger, Thomas M.Boston University School of Medicine, Boston, MAFANCA and FANCC Proteins Act Downstream of ATM and ATR, and Upstream of p53 in Telomere Overhang-induced DNA Damage Signals
Saïdi, Mado Pierre and Marie Curie Center, Alger, AlgeriaTo Report the Epidemiologic, Clinical, Biological Features and Course of Fanconi's Anemia in our Center
Saidj, Rachid Institut Curie-Recherche, Paris, FranceBRCA1 Controls Both DSB Repair Pathways: Homologous Recombination and DNA End-joining
Santos, Moema NenêUniversity of Paris, Hôpital Saint-Louis, Paris FranceDifferent Prevalence of Drug Metabolism Gene Polymorphisms (GSTP and GSTT) in Fanconi Anemia Patients Compared to a Normal Population
Schindler, DetlevUniversity of Wuerzburg, GermanyA Second Patient of Subtype FA-L: Diagnostic, Molecular and Cellular Findings
Smith, Franklin O.Cincinnati Childre's Hospital Medical Center and University of Cincinnati College of Medicine, Cincinnati, OHA Pilot Trial of Oxandrolone for the Treatment of Bone Marrow Failure for Patients with Fanconi Anemia
Soulier, Jean Hôpital Saint-Louis, Paris, FranceDiagnosis of Fanconi Anemia in Patients with Bone Marrow Failure
Tabah, Azah A.University of Minnesota, Minneapolis, MNThe Rad50, Mre11, and Nbs1 Complex Mediated DNA Tethering is Dependent on the Fanconi Anemia Signaling Pathway
Taniguchi, Toshiyasu Fred Hutchinson Cancer Research Center, Seattle, WAIdentification of Novel Factors Involved in the Fanconi Anemia Pathway Using Gene-trap Mutagenesis
Thuillier, Phillippe Oregon Health and Science University Cancer Research Center, Portland, ORInhibition of Ovarian Cancer Epithelial (FANCF Deficient) Cell Proliferation by the Chemopreventative Dietary Conjugated Linoleic Acid
Titus, Tom A.University of Oregon, Eugene, ORGenomic Conservation of the Fanconi Anemia Network in the Zebrafish, Danio rerio
Tönnies, Holger University of Berlin, GermanyAutomated I-FISH-Scanning Sensitively Detecting Early MDS- and AML- associated Chromosomal Imbalances in Peripheral Blood and Bone Marrow Cells of Fanconi Anemia Patients
Tsuchida, Ken Kyoto University, Kyoto, JapanRemoval of DNA Crosslinks is Normal in Both XP-A Cell and BRCA2-/- Cells, But not in Fanconi Anemia Cells
Wang, XiaoZhe Dana-Farber Cancer Institute, Harvard Medical School, Boston, MARegulation of the Fanconi Anemia Pathway by the Checkpoint ATR-CHK1 Pathway
Yamamoto, Kazuhiko Schneider Children's Hospital, New Hyde Park, NYHeightened Activation of the p53-ATM Axis in Fanconi Anemia Mutant-Derived Primary Cells: Implications for Carcinogenesis
Zatterale, Adriana Elena D'Aosta Hospital, Naples, ItalyFanconi Anemia in Italy: Lights and Shadows on Diagnostics, Clinical Governance and Epidemiology from the National Registry
Fanconi Anemia Research Fund, Inc. Fanconi Anemia Research Fund, Inc.