Evidence for at least eight Fanconi anemia genes.

No abstract is available for this paper.

• Publication year

  1997

• Venue

  American Journal of Human Genetics

• Publication date

  1997-10-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1086/514881PMID 9382107PMCID PMC1715980
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Fanconi Anemia

  2019cited by this paper
• Fanconi anemia genes act to suppress a cross-linker-inducible p53-independent apoptosis pathway in lymphoblastoid cell lines.

  1996cited by this paper
• Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA

  1996cited by this paper
• Positional cloning of the Fanconi anaemia group A gene.

  1996cited by this paper
• Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene.

  1996cited by this paper
• Suppression of apoptosis in hematopoietic factor-dependent progenitor cell lines by expression of the FAC gene.

  1996cited by this paper
• Fanconi anaemia in Italy: High prevalence of complementation group A in two geographic clusters

  1996cited by this paper
• Fanconi anaemia forges a novel pathway

  1996cited by this paper
• Positional cloning of the Fanconi anaemia group A gene

  1996cited by this paper
• Erratum: Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA

  1996cited by this paper
• Fanconi anaemia complementation groups in Germany and The Netherlands

  1996cited by this paper
• Germ cell defects and hematopoietic hypersensitivity to gamma- interferon in mice with a targeted disruption of the Fanconi anemia C gene

  1996cited by this paper
• Complementation groups: one or more per gene?

  1995cited by this paper
• Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype.

  1995cited by this paper
• Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p

  1995cited by this paper
• Localisation of the Fanconi anaemia complementation group A gene to chromosome 16q24.3

  1995cited by this paper
• Mutation analysis of the Fanconi anemia gene FACC.

  1994cited by this paper
• Incisions for excision

  1994cited by this paper
• Fanconi anemia and novel strategies for therapy.

  1994cited by this paper
• DNA repair. Incisions for excision.

  1994cited by this paper
• A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

  1993cited by this paper
• Cloning of cDNAs for Fanconi's anaemia by functional complementation

  1992cited by this paper
• Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9

  1992cited by this paper
• Identification of two complementation groups in Fanconi anemia

  1985cited by this paper
• Susceptibility of Fanconi's anemia lymphoblasts to DNA-cross-linking and alkylating agents.

  1982cited by this paper

• Genetic Testing of Japanese Patients with Serrated Polyposis Syndrome: A Multicentric Study

  2024cites this paper
• Beyond visualization of DNA double-strand breaks after radiation exposure

  2021cites this paper
• Prenatal Diagnosis of Radial Ray Defect Associated with Fanconi Anemia: a Case Report

  2020cites this paper
• Genetic syndromes with evidence of immune deficiency

  2020cites this paper
• ERCC1 mutations impede DNA damage repair and cause liver and kidney dysfunction in patients

  2020cites this paper
• Stem cell-derived clade F AAVs mediate high-efficiency homologous recombination-based genome editing

  2018cites this paper
• Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia.

  2017cites this paper
• A never-ending story: the steadily growing family of the FA and FA-like genes

  2017cites this paper
• Concurrent progress of reprogramming and gene correction to overcome therapeutic limitation of mutant ALK2-iPSC

  2016cites this paper
• Male fertility and skin diseases

  2016cites this paper
• FANCJ protein is important for the stability of FANCD2/FANCI proteins and protects them from proteasome and caspase-3 dependent degradation

  2015cites this paper
• Caractérisation cellulaire et moléculaire de FANCG : une protéine à la croisée entre l’anémie de Fanconi et la réparation de l’ADN

  2015cites this paper
• Cytogenetic Investigation in Prenatal Specimecimens for Effective Prognosis of Pregnancy Related Complications

  2014cites this paper
• Functional Characterisation of Human MUS81 Complexes

  2014cites this paper
• Reticulate pigmentary disorders.

  2013cites this paper
• Fanconi Anemia Founder Mutation in Macedonian Patients

  2013cites this paper
• of caspase 3 family members dependent activation - hematopoietic progenitor cells involve caspase 8 induced apoptotic responses of Fanconi anemia group C - γ Interferon-

  2013cites this paper
• Fanconi Anemia Group C Protein and PLZF A Novel BTB/POZ Transcriptional Repressor Protein Interacts With the

  2013cites this paper
• Chapter 160 – The Dysostoses

  2013cites this paper
• Bone Marrow Failure in the Fanconi Anemia Group C Mouse Model After

  2013cites this paper
• DNA Repair Capacity and the Risk of Head and Neck Cancer

  2012cites this paper
• Analyse des variants de séquence et d'épissage du gène FANCC chez les familles canadiennes-françaises à risque élevé pour le cancer du sein et/ou de l'ovaire

  2011cites this paper
• phase The Fanconi anemia core complex associates with chromatin during S

  2010cites this paper
• Use of murine models to test novel gene transfer strategies for the treatment of fanconi anemia

  2010cites this paper
• STRATEGIES FOR THE TREATMENT OF FANCONI ANEMIA

  2010cites this paper
• The genetic and molecular basis of Fanconi anemia.

  2009cites this paper
• Identification of putative interactors of Fanconi anaemia proteins by yeast to hybrid system: characterization of two novel genes highly expressed during spermatogenesis

  2009cites this paper
• What's in a cancer syndrome? Genes, phenotype and pathology

  2008cites this paper
• Molekulargenetische Untersuchungen des Fanconi Anämie C Gens bei Kindern mit malignen Erkrankungen

  2008cites this paper
• AMD3100 synergizes with G-CSF to mobilize repopulating stem cells in Fanconi anemia knockout mice.

  2008cites this paper
• Estudo das mutações do gene Fancc em pacientes com quadro clinico de anemia de Fanconi na região de Campinas

  2008cites this paper
• [Fanconi anemia: cellular and molecular features].

  2007cites this paper
• Fanconi Anemia Genes: Structure, Mutations, and Genotype-Phenotype Correlations

  2007cites this paper
• Overview of the DNA Damage Checkpoint

  2007cites this paper
• L'anémie de Fanconi : aspects cellulaires et moléculaires

  2007cites this paper
• Promoter hypermethylation of FANCF plays an important role in the occurrence of ovarian cancer through disrupting fanconi anemia-BRCA pathway

  2006cites this paper
• Expresión diferencial del ARN en la anemia de Fanconi. Una probable característica fenotípica

  2006cites this paper
• In vivo repopulation ability of genetically corrected bone marrow cells from Fanconi anemia patients

  2006cites this paper
• FANCD2 monoubiquitination and activation by hexavalent chromium [Cr(VI)] exposure: activation is not required for repair of Cr(VI)-induced DSBs.

  2006cites this paper
• Natural gene therapy in monozygotic twins with Fanconi anemia.

  2006cites this paper
• The FANC B, E, F and G Genes and Their Products

  2006cites this paper
• Aplasies médullaires constitutionnelles

  2006cites this paper
• FANCD2 associated with sporadic breast cancer risk.

  2006cites this paper
• The Fanconi Anemia Pathway of Genomic Maintenance

  2006cites this paper
• Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2.

  2006cites this paper
• The FANC Genome Surveillance Complex

  2006cites this paper
• Mutational Analyses of Fanconi Anemia Genes in Japanese Patients

  2006cites this paper
• The Fanconi anemia DNA maintenance pathway: focus on the FANCE and FANCF proteins

  2006cites this paper
• Genomic Instability in Fanconi Anaemia and Nijmegen Breakage Syndrome

  2006cites this paper
• Roles of the BRCA1 and BRCA2 Breast Cancer Susceptibility Proteins in DNA Repair

  2006cites this paper
• Overexpression of the Fanconi Anemia A Gene in Hela and MCF10A Cells

  2006cites this paper
• FANCD 2 associated with sporadic breast cancer risk

  2006cites this paper
• "Dub"bing a tumor suppressor pathway.

  2005cites this paper
• Homozygous germ line mutation in exon 27 of murine Brca2 disrupts the Fancd2–Brca2 pathway in the homologous recombination‐mediated DNA interstrand cross‐links' repair but does not affect meiosis

  2005cites this paper
• Fanconi anemia: Current management

  2005cites this paper
• Physiological and Pathological Growth Hormone Secretion

  2005cites this paper
• Identification of multiple nuclear export sequences in Fanconi anemia group A protein that contribute to CRM1-dependent nuclear export.

  2005cites this paper
• Regulated interaction of the Fanconi anemia protein, FANCD2, with chromatin.

  2005cites this paper
• Treatment options in early stages of Hodgkin's Lymphoma, high cure rate with lower short and long-term toxicity

  2005cites this paper
• The Fanconi anemia core complex associates with chromatin during S phase.

  2005cites this paper
• Topics in pediatric leukemia--Fanconi's anemia: new insights.

  2005cites this paper
• Post-irradiation phosphorylation of structural maintenance chromosome 1 (SMC1) is independent of the Fanconi protein pathway.

  2005cites this paper
• Nijmegen breakage syndrome diagnosed as Fanconi anaemia

  2005cites this paper
• The Caenorhabditis elegans FancD2 ortholog is required for survival following DNA damage.

  2005cites this paper
• Coinheritance of BRCA1 and BRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: Possible role in risk modification for cancer development

  2005cites this paper
• Haematologica 1998 ; 83 : 533-542 molecular basis of disease

  2005cites this paper
• 3R coordination by Fanconi anemia proteins.

  2005cites this paper
• Direct DNA Binding Activity of the Fanconi Anemia D2 Protein*

  2005cites this paper
• The genetic basis of bone marrow failure syndromes in children.

  2005cites this paper
• New Advances in the DNA Damage Response Network of Fanconi Anemia and BRCA proteins: FAAP95 Replaces BRCA2 as the True FANCB Protein

  2005cites this paper
• Fanconi Anemia Complementation Group D2 (FANCD2) Functions Independently of BRCA2- and RAD51-associated Homologous Recombination in Response to DNA Damage*

  2005cites this paper
• Intermediate DNA repair activity associated with the 322delG allele of the fanconi anemia complementation group C gene.

  2004cites this paper
• Identification and characterization of novel mutations of the major Fanconi anemia gene FANCA in the Japanese population

  2004cites this paper
• Genetics of the FANCA gene in familial pancreatic cancer

  2004cites this paper
• Oxidative Stress/Damage Induces Multimerization and Interaction of Fanconi Anemia Proteins*

  2004cites this paper
• Interstrand crosslink-induced radials form between non-homologous chromosomes, but are absent in sex chromosomes.

  2004cites this paper
• phase The Fanconi anemia core complex associates with chromatin during S

  2004cites this paper
• Telomere dysfunction in genome instability syndromes.

  2004cites this paper
• Fanconi anemia in Ashkenazi Jews

  2004cites this paper
• Inherited Bone Marrow Failure

  2004cites this paper
• Jun N-terminal kinase activity and early growth-response factor-1 gene expression are down-regulated in Fanconi anemia group A lymphoblasts.

  2004cites this paper
• The Fanconi Anemia Core Complex Forms Four Complexes of Different Sizes in Different Subcellular Compartments*

  2004cites this paper
• Phosphorylation of Fanconi Anemia (FA) Complementation Group G Protein, FANCG, at Serine 7 Is Important for Function of the FA Pathway*

  2004cites this paper
• Multiple TPR motifs characterize the Fanconi anemia FANCG protein.

  2004cites this paper
• Cytogenetic characteristics of oral squamous cell carcinomas in Fanconi anemia

  2004cites this paper
• Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemia

  2004cites this paper
• Lack of Sensitivity of Primary Fanconi's Anemia Fibroblasts to UV and Ionizing Radiation

  2004cites this paper
• FANCG Is Phosphorylated at Serines 383 and 387 during Mitosis

  2004cites this paper
• Heterogeneity in Fanconi anemia: evidence for 2 new genetic subtypes.

  2004cites this paper
• Fanconi Anemia: Contribution of Molecular Analyses to the Identification of Bone Marrow Graft Donors and the Study of Chimerism in Grafted Patients

  2004cites this paper
• A Rad50-dependent pathway of DNA repair is deficient in Fanconi anemia fibroblasts.

  2004cites this paper
• The p38 pathway partially mediates caspase-3 activation induced by reactive oxygen species in Fanconi anemia C cells.

  2004cites this paper
• Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways.

  2004cites this paper
• The interplay of Fanconi anemia proteins in the DNA damage response.

  2004cites this paper
• Impairment of homologous recombination control in a Fanconi anemia‐like Chinese Hamster Cell mutant

  2004cites this paper
• Heterogeneity in Fanconi anemia : evidence for 2 new genetic subtypes

  2004cites this paper
• Fanconi ’ s anemia Author : Doctor

  2003cites this paper
• Sorting out the cellular functions of sorting nexins

  2003cites this paper
• Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations

  2003cites this paper
• Deficient Regulation of DNA Double-strand Break Repair in Fanconi Anemia Fibroblasts*

  2003cites this paper