Identification of two complementation groups in Fanconi anemia

No abstract is available for this paper.

• Publication year

  1985

• Venue

  Somatic Cell Genetics

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/BF01534732PMID 3919452
• 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.

• Complementation studies between Fanconi's anemia cells with different DNA repair characteristics

  2004cited by this paper
• Analysis of heterogeneity in Fanconi's anemia patients of different ethnic origin

  2004cited by this paper
• Suppression of spontaneous and mitomycin C-induced chromosome aberrations in Fanconi's anemia by cell fusion with normal human fibroblasts

  2004cited by this paper
• Clinical and cytogenetic diversity in Fanconi's anaemia.

  1984cited by this paper
• Genetic heterogeneity in ataxia-telangiectasia studied by cell fusion.

  1982cited by this paper
• Susceptibility of Fanconi's anemia lymphoblasts to DNA-cross-linking and alkylating agents.

  1982cited by this paper
• Spectrum of anomalies in Fanconi anaemia.

  1982cited by this paper
• Survey of radiosensitivity in a variety of human cell strains.

  1980cited by this paper
• X-ray sensitivity of fifty-three human diploid fibroblast cell strains from patients with characterized genetic disorders.

  1980cited by this paper
• Genetic heterogeneity of Fanconi's anemia demonstrated by somatic cell hybrids

  1980cited by this paper
• Specific cellular defects in patients with Fanconi anemia

  1979cited by this paper
• Formal genetics of Fanconi's anemia

  1976cited by this paper
• Ouabain-resistant mutants of mouse and hamster cells in culture

  1974cited by this paper
• A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents.

  1973cited by this paper
• In vitro chromosomal radiosensitivity in “chromosomal breakage syndromes”

  1973cited by this paper
• Genetic heterogeneity of xeroderma pigmentosum demonstrated by somatic cell hybridization.

  1972cited by this paper
• Fanconi's Anaemia in the Genetics of Neoplasia

  1971cited by this paper
• [Spontaneous chromosome aberrations in familial panmyelopathy].

  1964cited by this paper

• Ovarian Failure Preceding Head and Neck Squamous Cell Carcinoma Identifies an Adult-Onset Cancer-Prone Syndrome Caused by FANCM Mutations.

  2021cites this paper
• Fanconi Anemia

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

  2017cites 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
• From the Molecular Biology to the Gene Therapy of a DNA Repair Syndrome: Fanconi Anemia

  2011cites this paper
• Gene Therapy of Some Genetic Diseases by Transferring Normal Human Genomic DNA into Somatic Cells and Stem Cells from Patients

  2011cites this paper
• Genetic Basis of Inherited Bone Marrow Failure Syndromes

  2011cites this paper
• Marrow failure syndromes

  2010cites this paper
• A possible approach for stem cell gene therapy of Fanconi anemia.

  2009cites this paper
• Monoketone analogs of curcumin, a new class of Fanconi anemia pathway inhibitors

  2009cites this paper
• Estudo das mutações do gene Fancc em pacientes com quadro clinico de anemia de Fanconi na região de Campinas

  2008cites this paper
• L'anémie de Fanconi : aspects cellulaires et moléculaires

  2007cites this paper
• [Fanconi anemia: cellular and molecular features].

  2007cites this paper
• Why, What and How Can We Learn from a Rare Disease Like Fanconi Anemia?

  2007cites this paper
• Aplasies médullaires constitutionnelles

  2006cites this paper
• The use of fluoroquinolones in children

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

  2006cites this paper
• Advances in understanding the genetic basis for bone-marrow failure.

  2006cites this paper
• The FANC Genome Surveillance Complex

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

  2006cites this paper
• 3R coordination by Fanconi anemia proteins.

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

  2005cites this paper
• Fanconi's anaemia: correlation of genetic complementation group with psoralen/UVA response

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

  2004cites this paper
• Mapping of the murine and rat Facc genes and assessment of flexed-tail as a candidate mouse homolog of Fanconi anemia group C

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

  2004cites this paper
• Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool.

  2002cites this paper
• Fanconi anemia group A and C double-mutant mice: functional evidence for a multi-protein Fanconi anemia complex.

  2002cites this paper
• The role of reactive oxygen and nitrogen species in the development of Fanconi Anemia, an inherited bone marrow failure disorder

  2002cites this paper
• Constitutional Hypoplastic Anemia

  2002cites this paper
• Current Knowledge on the Pathophysiology of Fanconi Anemia: From Genes to Phenotypes

  2001cites this paper
• Fanconi Anemia Pathway and Cancer Susceptibility

  2001cites this paper
• Fanconi anemia and DNA repair.

  2001cites this paper
• Preclinical protocol for in vivo selection of hematopoietic stem cells corrected by gene therapy in Fanconi anemia group C.

  2001cites this paper
• The Inherited Bone Marrow Failure Syndromes: Fanconi Anemia, Dyskeratosis Congenita and Diamond‐Blackfan Anemia

  2000cites this paper
• Aplasies médullaires constitutionnelles

  2000cites this paper
• Aplasias medulares constitucionales

  2000cites this paper
• The genetics of Fanconi's anaemia.

  2000cites this paper
• Cloning and characterization of murine Fanconi anemia group A gene: Fanca protein is expressed in lymphoid tissues, testis, and ovary

  2000cites this paper
• Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A.

  2000cites this paper
• Fanconi anemia and βc deficiency-associated pulmonary alveolar proteinosis as two hereditary diseases of childhood which are potentially curable by stem cell gene therapy but require different therapeutic approaches

  1999cites this paper
• Drug sensitivity spectra in Fanconi anemia lymphoblastoid cell lines of defined complementation groups.

  1999cites this paper
• Diagnosis of Chromosomal Instability Syndromes

  1999cites this paper
• The molecular and cellular biology of Fanconi anemia.

  1999cites this paper
• Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene

  1999cites this paper
• In vivo selection of wild-type hematopoietic stem cells in a murine model of Fanconi anemia.

  1999cites this paper
• Genetic disorders associated with cancer predisposition and genomic instability.

  1999cites this paper
• [Fanconi disease: study of 43 cases in southern Tunisia].

  1998cites this paper
• Genetic predisposition to genomic instability in cancer.

  1998cites this paper
• La maladie de Fanconi: étude de 43 cas dans le sud tunisien

  1998cites this paper
• Is Fanconi anemia caused by a defect in the processing of DNA damage?

  1998cites this paper
• Molecular basis of Fanconi anemia.

  1998cites this paper
• Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining.

  1998cites this paper
• Gene transfer for the eventual treatment of Fanconi's anemia.

  1998cites this paper
• MxA overexpression reveals a common genetic link in four Fanconi anemia complementation groups.

  1997cites this paper
• Evidence for at least eight Fanconi anemia genes.

  1997cites this paper
• Complementation group assignments in fanconi anemia fibroblast cell lines from North America

  1997cites this paper
• Molecular biology of Fanconi anemia: implications for diagnosis and therapy.

  1997cites this paper
• Functional correction of Fanconi anemia group A hematopoietic cells by retroviral gene transfer.

  1997cites this paper
• Cytoplasmic localization of a functionally active Fanconi anemia group A-green fluorescent protein chimera in human 293 cells.

  1997cites this paper
• Applicability of nonsyngeneic cell models for screening of genes in monogenetics diseases via differential display technique

  1997cites this paper
• The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2.

  1997cites this paper
• The fidelity of double strand breaks processing is impaired in complementation groups B and D of fanconi anemia, a genetic instability syndrome

  1997cites this paper
• Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene.

  1996cites this paper
• Developmental expression of the Fac gene correlates with congenital defects in Fanconi anemia patients.

  1996cites this paper
• Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations

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

  1996cites this paper
• Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity.

  1996cites this paper
• The effect of the Fanconi anemia polypeptide, FAC, upon p53 induction and G2 checkpoint regulation.

  1996cites this paper
• Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells.

  1996cites this paper
• Correction of Fanconi Anemia Type C Phenotypic Abnormalities Using a Clinically Suitable Retroviral Vector Infection Protocol

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

  1996cites this paper
• Assessment of the flexed-tail mouse as a possible model for Fanconi anemia: analysis of mitomycin C-induced micronuclei.

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

  1996cites this paper
• Halogen analogs of thymidine increase the level of chromosome aberrations in cells of patients with Fanconi's anemia

  1996cites this paper
• Clonal chromosome abnormalities in Fanconi anemia.

  1996cites this paper
• Molecular insights into Fanconi anemia.

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

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

  1996cites this paper
• Correction of the spontaneous and DEB-induced chromosomal aberrations in Fanconi anemia cells of the FA(C) complementation group by the FACC gene.

  1996cites this paper
• Correction of Fanconi anemia type C phenotypic abnormalities using a clinically suitable retroviral vector infection protocol.

  1996cites this paper
• Fanconi’s anaemia

  1996cites this paper
• Fanconi anemia genes act to suppress a cross-linker-inducible p53-independent apoptosis pathway in lymphoblastoid cell lines.

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

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

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

  1995cites this paper
• Identification of Cytosolic Proteins That Bind to the Fanconi Anemia Complementation Group C Polypeptide in Vitro

  1995cites this paper
• Fanconi anemia and novel strategies for therapy.

  1994cites this paper
• FANCONI'S ANAEMIA AND ITS VARIABILITY

  1994cites this paper
• Molecular Mechanisms Responsible for Repair of Adducts Induced in Human Cellular DNA by Puva

  1994cites this paper
• Comparison of the effects of DNA topoisomerase inhibitors on lymphoblasts from normal and Fanconi anemia donors.

  1994cites this paper
• Identification and chromosomal localization of a DNA fragment implicated in the partial correction of the Fanconi anemia group D cellular defect.

  1994cites this paper
• Comparative study of Fanconi anemia in children of different ethnic origin in South Africa.

  1994cites this paper
• Hemoglobin F synthesis is not restricted to fetal erythropoietic organs during extramedullary hematopoiesis.

  1994cites this paper
• Mutagenic response and repair of cis-DDP-induced DNA cross-links in the Chinese hamster V79 cell mutant V-H4 which is homologous to Fanconi anemia (group A).

  1994cites this paper
• Apoptosis is not involved in the hypersensitivity of Fanconi anemia cells to mitomycin C.

  1994cites this paper
• Fanconi anemia revisited: Old ideas and new advances

  1994cites this paper
• Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells.

  1994cites this paper
• Mutagenic processing of psoralen monoadducts differ in normal and Fanconi anemia cells.

  1993cites this paper
• Human genetic instability syndromes: single gene defects with increased risk of cancer.

  1993cites this paper