Fanconi Anemia Scientific Symposium Poster Presentations
September 29th - October 2 , Geneva, Switzerland
Alter, Blanche P. National Cancer Institute, Rockville, MD Cancer 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, OH Monoubiquitinated FANCD2 Recruits the Machinery for Homologous Recombination to the Replication Fork: Implications for the Etiology of Fanconi Anemia
Baker, Jillian The 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, Delphine Gustave 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, Spain Severe Hematopoietic Stem Cell Defects in Mice with a Hypomorphic Mutation in Brca2
Calzone, Rita Elena D'Aosta Hospital, Naples, Italy Cytological Aspects Leading to New Interpretations in Fanconi Anemia Cellular Biology
Camboni, Maria Gavina Institute of Biomolecular Chemistry, Sassari, Italy Expression Analysis of FANCG and FANCC Genes in Sporadic Colon Cancer
Camelo, Ricardo Mesquita Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, Brazil Amifostine Protection against Mitomycin-induced Chromosomal Breakage in Fanconi Anaemia Lymphocytes
Cantor, Sharon B. University of Massachusetts Cancer Center, Worcester, MA BACH1 is Critical for Homologous Recombination and Appears to be the Fanconi Anemia Gene Product FANCJ
Chuang, Alice Y. C. Johns Hopkins Medical Institution, Baltimore, MD p53 Inactivation Results in Chromosomal Instability and the Presence of Telomere DNA in Interphase Bridges
Chuang, Tony Johns Hopkins Medical Institution, Baltimore, MD Three Dimensional Organization of Telomeres in Head and Neck Cancer
Collis, Spencer The London Research Institute, Clare Hall Laboratories, South Mimms, United Kingdom Functional Analysis of the C. elegans FANCD2 Homologue
Constantinou, Angelos University of Lausanne, Epalinges, Switzerland Defining the Connections between FA Proteins, DNA Replication and DNA Lesions
de Vries, Yne Waterham Vrije University Medical Center, Amsterdam, The Netherlands Evidence for a New Complementation Group with a Defect Downstream in the Fanconi Anemia Pathway
Dufour, Carlo G. Gaslini Children’s Hospital, Genoa, Italy Role 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, Nupur University of Pittsburgh, Pittsburgh, PA Notch Ligand (Delta-like-1) Can Support the Development of Bone Marrow Stem Cells
Gluckman, Eliane Hôpital Saint-Louis, Paris, France Potentials and Limits of Gene Therapy in Fanconi Anemia
Gökçora, I. Haluk Cebeci Hospital, Dikimevi, Ankara, Turkey A Case of Fanconi’s Anemia with an Initial Presentation of Abdominal Rhabdomyosarcoma
Howlett, Niall G. University of Michigan, Ann Arbor, MI The Fanconi Anemia Pathway is Required for the DNA Replication Stress Response and for the Regulation of Common Fragile Site Stability
Hutchinson, Amy Ann National Cancer Institute, Gaithersburg, MD Sequence 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, UK Characterisation 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, OH Collection 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, OH Gene Transfer for Patients with Fanconi Anemia, Genotype A: A Pilot Study
Kitao, Hiroyuki Kawasaki Medical School, Okayama, Japan Functional Relationship between FANCD1/BRCA2-Rad51 Pathway and the Fanconi Anemia Pathway in DNA Repair
Kluzek, Katarzyna Nicolaus Copernicus University, Bydgoszcz, Poland Chinese Hamster Cell Mutant CL-V5B is Defective in the Fancc Gene
Krejci, Lumir Yale 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, IN Fanconi 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, UK EVI1 Amplification in FA-derived AML Cell Lines with Bi-allelic FANCD1/BRCA2 Mutations
Meyer, Stefan Central Manchester and Manchester Children's University Hospital NHS Trust, Manchester, UK No Evidence of Significant FANCF Methylation in Sporadic Acute Childhood Leukaemia
Morgese, Fabio Telethon Institute of Genetics and Medicine, Naples Italy Characterization of Two Novel Interactors of the Fanconi Anemia Protiens
Mosedale, Georgina MRC Laboratory of Molecular Biology, Division of Protein and Nucleic Acid Chemistry, Cambridge, UK The Ku70 Protein Subverts Homologous Recombination Repair Following Inactivation of the Fanconi Anaemia Pathway
Nakanishi, Koji Memorial Sloan-Kettering Cancer Center, New York, NY FA Pathway and Double-strand Break Repair
Navarro, Susana CIEMAT, Madrid, Spain A Fast and Reliable Procedure for the Genotyping Fanconi Anemia Knockout Mice Using Melting Curves Analysis From Multiplex qPCR
Neveling, Kornelia University of Würzburg, Germany Fanconi Anemia Mutation Screen in Bladder Carcinoma.
O'Donnell, Paul Fred Hutchinson Cancer Research Center, Seattle, WA Nonmyeloablative Hematopoietic Cell Transplantation of Advanced Hematologic Malignancies using Haploidentical Donors
Olsen, Anna John Radcliffe Hospital, Oxford, UK Processsing of Interstrand Cross-links by Excision Repair Factors: Impact on Activation of the Fanconi Anemia Pathway
Papadopoulo, Dora Institute Curie, Research Division, Paris, France FANC Genes and Double Strand Break Repair
Patel, K.J. MRC Laboratory of Molecular Biology, Division of Protein and Nucleic Acid Chemistry, Cambridge, UK The 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, UK Progress 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, MA Structural Studies of FANCE and FANCD2 Proteins
Roomi, M. Waheed Matthias Rath Research Institute, Santa Clara, CA Down 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, MA FANCA 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, Algeria To Report the Epidemiologic, Clinical, Biological Features and Course of Fanconi's Anemia in our Center
Saidj, Rachid Institut Curie-Recherche, Paris, France BRCA1 Controls Both DSB Repair Pathways: Homologous Recombination and DNA End-joining
Santos, Moema Nenê University of Paris, Hôpital Saint-Louis, Paris France Different Prevalence of Drug Metabolism Gene Polymorphisms (GSTP and GSTT) in Fanconi Anemia Patients Compared to a Normal Population
Schindler, Detlev University of Wuerzburg, Germany A 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, OH A Pilot Trial of Oxandrolone for the Treatment of Bone Marrow Failure for Patients with Fanconi Anemia
Soulier, Jean Hôpital Saint-Louis, Paris, France Diagnosis of Fanconi Anemia in Patients with Bone Marrow Failure
Tabah, Azah A. University of Minnesota, Minneapolis, MN The Rad50, Mre11, and Nbs1 Complex Mediated DNA Tethering is Dependent on the Fanconi Anemia Signaling Pathway
Taniguchi, Toshiyasu Fred Hutchinson Cancer Research Center, Seattle, WA Identification of Novel Factors Involved in the Fanconi Anemia Pathway Using Gene-trap Mutagenesis
Thuillier, Phillippe Oregon Health and Science University Cancer Research Center, Portland, OR Inhibition of Ovarian Cancer Epithelial (FANCF Deficient) Cell Proliferation by the Chemopreventative Dietary Conjugated Linoleic Acid
Titus, Tom A. University of Oregon, Eugene, OR Genomic Conservation of the Fanconi Anemia Network in the Zebrafish, Danio rerio
Tönnies, Holger University of Berlin, Germany Automated 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, Japan Removal 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, MA Regulation of the Fanconi Anemia Pathway by the Checkpoint ATR-CHK1 Pathway
Yamamoto, Kazuhiko Schneider Children's Hospital, New Hyde Park, NY Heightened Activation of the p53-ATM Axis in Fanconi Anemia Mutant-Derived Primary Cells: Implications for Carcinogenesis
Zatterale, Adriana Elena D'Aosta Hospital, Naples, Italy Fanconi 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.