| Afghani,
Tayyab |
Al-Shifa
Trust Eye Hospital, Rawalpindi, Pakistan |
Fanconi’s Anemia Presenting as Microphthalmos with Orbital Cyst
|
|
Ali, Abdullah |
Cincinnati
Children's Hospital Medical Center, Cincinnati, Ohio |
An Unusual Presentation of FANCL: Making the Case for
Complementation Analysis in All Fanconi Anemia Patients
|
|
Alter, Blanche |
National
Cancer Institute, Rockville, Maryland
|
Cancer Epidemiology in the National Cancer Institute Fanconi Anemia
Cohort |
Auerbach, Arleen
|
The
Rockefeller University, New York, New York
|
New FA Genes in IFAR Patients from North America: 25 Year Update
and Genotype/Phenotype Correlations |
Bakker, Sietske
|
Netherlands Cancer
Institute, Amsterdam, The Netherlands
|
Characterization of the Knockout Mouse and MEF019s for Fancm |
|
Bierings, Marc
|
University
Children's Hospital Utrecht, Utrecht, The Netherlands |
The First Dutch National Guideline for the Treatment of Fanconi
Anemia
|
Bitan, Menachem
|
Tel-Aviv
Sourasky Medical Center, Tel-Aviv, Israel |
Fludarabine-busulfex Combination as Part of the Conditioning for
Allogeneic Stem Cell Transplantation in Fanconi Anemia
|
Bonfim, Carmem
|
Federal
University of Parana, Parana, Brazil |
Long Term Follow-up after Stem Cell Transplantation in Fanconi
Anemia: Analysis of 52 Patients Transplanted at a Single Center
|
Brunet, Erika
|
Memorial
Sloan-Kettering Cancer Center, New York, New York |
FANCG Suppresses Chromosomal Translocations Induced by Targeted
DNA Double-strand Breaks
|
Castella, Maria
|
Universitat
Autonoma de Barcelona, Barcelona, Spain |
Characterization of a Large Deletion Found in a FA-A Patient involving
FANCA, SPIRE2 and TCF25 Genes
|
Casula, Milena
|
Istituto
di Chimica Biomolecolare, Sassari, Italy
|
Fanconi Genes are Altered in Subsets of Patients with Sporadic
Colorectal Carcinoma |
Cherubini, Gioia
|
Institut
Gustave Roussy, Villejuif, France |
Adenovirus: A New Tool to Understand the Role of FANCD2 in
Replication
|
|
Fei, Peiwen
|
Mayo
Clinic College of Medicine, Rochester, Minnesota |
FANCD2 Monoubiquitination Provides a Link between the HHR6 and
FA-BRCA Pathways
|
Ferrara, Mara
|
Second
University of Naples, Naples, Italy |
Incidence
of Malignancy in FA Heterozygotes
|
| Flores-Obando,
Rafael |
University of Pittsburgh
Graduate School of Public Health, Pittsburgh, Pennsylvania |
Altered FANCD2 Monoubiquitination in Squamous Cell Carcinoma of
the Head and Neck Cell Lines
|
Gangopadhyay, Nupur
|
University
of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania
|
Lymphoid Progenitor Cells can Facilitate Allogeneic Bone Marrow
Transplantation |
Giri,
Neelam
|
National Cancer Institute,
Rockville, Maryland |
Pituitary Size and Endocrine Function in Fanconi Anemia
|
Godthelp, Barbara
|
Leiden
University Medical Center, Leiden, The Netherlands
|
Mitomycin C Hypersensitivity in Cornelia de Lange Syndrome Cells:
Role for Cohesins in DNA Interstrand Crosslink Repair |
Guervilly, Jean-Hugues
|
Institut
Gustave Roussy, Villejuif, France
|
Interactions between the ATR Network and the FA Pathway |
Hamidieh, Amir
|
Tehran
University of Medical Sciences, Tehran, Iran |
Hematopoietic Stem Cell Transplantation (HSCT) in Fanconi Anemia
from Iran: Outcome of 24 Patients
|
Hays, Laura
|
Oregon
Health & Science University Cancer Institute, Portland, Oregon |
The Role of FANCD2 Suppression in Lung Carcinogenesis
|
Jacome, Ariana
|
CIEMAT,
Madrid, Spain |
Predictive Repopulation Value of CD34+ and Colony Forming Cells
Determinations in the Bone Marrow of FA Patients
|
Jacquemont, Celine
|
Fred Hutchinson Cancer Research Center, Seattle, Washington |
Proteasome Function is Required for the Activation of the Fanconi
Anemia Pathway and Homologous Recombination
|
|
Jones, Nigel |
University of Liverpool,
Liverpool, United Kingdom |
The Role of FANCG in Mediating the Formation of a Protein Complex
Containing BRCA2, FANCD2 and XRCC3 (D1-D2-G-X3)
|
|
Lambert, Muriel |
University of Medicine and Dentistry of New Jersey, Newark, New Jersey |
Deficiency in Incisions Produced by XPF at Sites of a DNA Interstrand
Cross-link in Fanconi Anemia Cells
|
Landais, Igor
|
Oregon Health & Science University, Portland, Oregon |
A Xenopus Cell-free Assay for Screening of Compounds that Modulate
the Fanconi Anemia Pathway
|
|
Mankad, Anuj |
Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio
|
Characterization of the Effect of FANCA Mutations on Biochemical and
Cellular Functionality |
Meyer, Stefan
|
University of Manchester, Manchester, United Kingdom |
High MN1 Expression in Fanconi Anaemia Derived Acute Myeloid
Leukaemia
|
|
Moghrabi, Nabil |
Oregon Health & Science University,
Portland, Oregon |
Validation of Fanconi Anemia Complementation Group Assignment by
Molecular Genetic Analysis
|
|
Mohan, Sheila
|
Apollo Specialty Hospital, Chennai, India
|
Dermatoglyphics in Fanconi Anemia Homozygotes and Heterozygotes |
Mohan, Sheila
|
Apollo Specialty
Hospital, Chennai, India
|
A Rare Case of Fanconi Anaemia with Paroxysmal Nocturnal
Hemoglobinuria |
Moses, Robb
|
Oregon Health &
Science University, Portland, Oregon
|
BRAFT Component, TopoIIIalpha, Functions Epistatically with the FA
Pathway |
Mseddi, Sondes
|
Hedi Chaker Hospital, Sfax, Tunisia |
Fanconi Anemia with Precocious and Inaugural Oncologic Events:
Implication of Complementation Group D1, about 2 C
|
Muller, Lars
|
Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio |
A Dual Approach to Enhance Engraftment of Fanconi Anemia HSC
Employing Rapid Transduction and in Vivo Selection
|
|
Neveling, Kornelia |
University of Wurzburg,
Wurzburg, Germany
|
Unusual Pattern of Genetic Alterations in the Rare FANCE Gene |
|
Oliveira, Vasco |
Moffit Cancer Center,
Tampa, Florida |
NF-kB as a Regulator of FA/BRCA Gene Expression in Multiple
Myeloma
|
|
Pagano, Giovanni |
Italian Association for Fanconi Anemia Research, Naples, Italy |
Regulation of Redox-related RNAs from FA Transcriptome Consortium
Suggests a Prooxidant State in FA Patients
|
|
Pals, Gerard |
Vrije Universiteit Medical Center, Amsterdam, The Netherlands |
Functional Analysis of Mutations in the FANC-A Gene
|
Rio, Paula
|
CIEMAT, Madrid, Spain |
Preclinical Gene Therapy Studies of Fanconi Anemia Patients (FA-A)
with Lentiviral Vectors Designed for Clinical Trials
|
Roomi, M. Waheed
|
Mathia Rath Research Institute, Santa Clara, California |
A Novel Nutrient Mixture Induces Apoptosis in Human FA Fibroblast
Cell Lines FA-A:PD220 and FA-D2:PD20
|
|
Schindler, Detlev |
University of Wurzburg, Wurzburg, Germany
|
Hematopoietic Mosaicism in FA: More Questions than Answers |
Shukla, Rashmi
|
All India Institute of Medical Sciences, New Delhi, India |
Mitomycin C Induced Chromosome Breakage and Phenotype
Variability in Suspected Fanconi Anemia Patients: AIIMS Experience
|
Singh, Thiyam Ramsing
|
Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio
|
BLAP18 is New Member of the BRAFT Complex
|
Smogorzewska, Agata
|
Harvard Medical School, Boston, Massachusetts
|
Identification and Characterization of FANCI, A Novel Component of
the Fanconi Anemia Pathway |
|
Thakar, Monica |
Fred Hutchinson
Cancer Research Center, Seattle, Washington |
HLA-Matched Unrelated Donor Stem Cell Transplantation Using Low-
Dose TBI and FLU for FA Patients with Aplastic Anemia
|
|
Tonnies, Holger |
University Clinic Schleswig-Holstein, Kiel, Germany |
New Molecular-cytogenetic Approach for the Quantitative and
Qualitative Analysis of Chromosomal Instability in FA Cells
|
|
Unal, Sule
|
Hacettepe University, Ankara, Turkey |
Renal Abnormalities in Fanconi Anemia Patients
|
|
Wells, Susanne
|
Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio
|
The High Risk HPV E7 Protein Mediates Coordinate Regulation of
Fanconi Anemia Genes through the Rb/E2F Pathway
|
|
Xie, Jenny |
University of Massachusetts Medical School, Worchester, Massachusetts |
FANCJ Displaces MutL 3B1 from DNA to Enhance Mismatch
Processing
|
|
Xu, Dongyi
|
National Institute on Aging, Baltimore, Maryland |
A New Component of the BRAFT Complex is Essential for Maintenance
of Genome Stability and BLM Function
|
|
Zatterale, Adriana |
Osp. Elena d'Aosta, Napoli, Italy
|
Down-regulation of Mitochondrial Activity, Glycolysis and Fatty Acid
Metabolism: from the FA Transcriptome Consortium |
|
Zhang, Xiaoling |
Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio |
Defective Adhesion, Migration and Homing Associated with Altered
Rho GTPase Activity in Cells from FA Patients
|
|
Zierhut, Heather |
University of Minnesota Medical Center, Minneapolis, Minnesota |
Role of a Genetic Counselor in an FA Comprehensive Care Program:
Summary and Patient Assessment at the University of Minnesota
|
| Fanconi
Anemia Research Fund Inc. |
