(Q24678530)

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Fanconi anaemia

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Europe PubMed Central

Fanconi anaemia (English)

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author name string

M D Tischkowitz

1

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S V Hodgson

2

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publication date

January 2003

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Journal of Medical Genetics

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40

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1

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1-10

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FANCC interacts with Hsp70 to protect hematopoietic cells from IFN-gamma/TNF-alpha-mediated cytotoxicity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Molecular and genealogical evidence for a founder effect in Fanconi anemia families of the Afrikaner population of South Africa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

The Fanconi anemia protein FANCC binds to and facilitates the activation of STAT1 by gamma interferon and hematopoietic growth factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

A novel BTB/POZ transcriptional repressor protein interacts with the Fanconi anemia group C protein and PLZF

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

High frequency of large intragenic deletions in the Fanconi anemia group A gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

The Fanconi anaemia group G gene FANCG is identical with XRCC9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Molecular chaperone GRP94 binds to the Fanconi anemia group C protein and regulates its intracellular expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

The Fanconi anaemia proteins, FAA and FAC, interact to form a nuclear complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Evidence for at least eight Fanconi anemia genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Sequence variation in the Fanconi anemia gene FAA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Convergence of the fanconi anemia and ataxia telangiectasia signaling pathways

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Reduced fertility and hypersensitivity to mitomycin C characterize Fancg/Xrcc9 null mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

The FANCG Fanconi anemia protein interacts with CYP2E1: possible role in protection against oxidative DNA damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Chromosomal breakage syndromes and the BRCA1 genome surveillance complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Review of oxymetholone: a 17alpha-alkylated anabolic-androgenic steroid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Fanconi anemia group C protein prevents apoptosis in hematopoietic cells through redox regulation of GSTP1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Preimplantation diagnosis for Fanconi anemia combined with HLA matching

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Human alpha spectrin II and the FANCA, FANCC, and FANCG proteins bind to DNA containing psoralen interstrand cross-links

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

The emerging genetic and molecular basis of Fanconi anaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Positional cloning of a novel Fanconi anemia gene, FANCD2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Mice with a targeted disruption of the Fanconi anemia homolog Fanca

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Cloning and characterization of murine fanconi anemia group A gene: Fanca protein is expressed in lymphoid tissues, testis, and ovary

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

The Fanconi anaemia gene FANCF encodes a novel protein with homology to ROM

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

SNX5, a new member of the sorting nexin family, binds to the Fanconi anemia complementation group A protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Human alpha spectrin II and the Fanconi anemia proteins FANCA and FANCC interact to form a nuclear complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Engraftment of hematopoietic progenitor cells transduced with the Fanconi anemia group C gene (FANCC)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Intracellular localization of the Fanconi anemia complementation group A protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Long-term bone marrow culture in Fanconi's anaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Carrier frequency of the IVS4 + 4 A-->T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Involvement of Brca2 in DNA repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Biallelic inactivation of BRCA2 in Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

7 April 2017

Fanconi anaemia syndrome and apoptosis: state of the art.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

DNA damage processing defects and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Fanconi anemia and DNA repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Somatic mosaicism in Fanconi anemia: evidence of genotypic reversion in lymphohematopoietic stem cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Fludarabine-based stem cell transplantation protocol for Fanconi's anaemia in myelodysplastic transformation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Damage-resistant DNA synthesis in Fanconi anemia cells treated with a DNA cross-linking agent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Arrest of S-phase progression is impaired in Fanconi anemia cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Diamond-Blackfan Anaemia: an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

The clinical and radiological features of Fanconi's anaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Fanconi anemia, complementation group A, cells are defective in ability to produce incisions at sites of psoralen interstrand cross-links

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Selective pressure as an essential force in molecular evolution of myeloid leukemic clones: a view from the window of Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Abnormal rearrangements associated with V(D)J recombination in Fanconi anemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Fanconi anemia C gene product plays a role in the fidelity of blunt DNA end-joining

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Mutations of the Fanconi anemia group A gene (FAA) in Italian patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

The sensitivity of Fanconi anaemia group C cells to apoptosis induced by mitomycin C is due to oxygen radical generation, not DNA crosslinking

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Revised classification of acute myeloid leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Hematologic abnormalities in Fanconi anemia: an International Fanconi Anemia Registry study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

The expression of cytokine and cytokine receptor genes in long-term bone marrow culture in congenital and acquired bone marrow hypoplasias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Thrombocytopenia with absent radii. A review of 100 cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Fanconi's anaemia and pregnancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Leukemia and preleukemia in Fanconi anemia patients. A review of the literature and report of the International Fanconi Anemia Registry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Formal genetics of Fanconi's anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Effects of alkylating agents on lymphocytes from controls and from patients with Fanconi's anemia. Studies of sister chromatid exchanges, chromosome aberrations, and kinetics of cell division

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Fanconi's anemia and malignancies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 September 2017

Nijmegen breakage syndrome: clinical characteristics and mutation analysis in eight unrelated Russian families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

Phenotypic consequences of mutations in the Fanconi anemia FAC gene: an International Fanconi Anemia Registry study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

Deregulated apoptosis is a hallmark of the Fanconi anemia syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

In-vivo assessment of DNA ligation efficiency and fidelity in cells from patients with Fanconi's anemia and other cancer-prone hereditary disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

Reassessment of cancer predisposition of Fanconi anemia heterozygotes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

Squamous cell carcinoma in the immunosuppressed patient: Fanconi's anemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

Abnormal lymphokine production: a novel feature of the genetic disease Fanconi anemia. I. Involvement of interleukin-6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

Susceptibility of Fanconi's anaemia fibroblasts to chromosome damage by carcinogens

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

30 May 2018

Fanconi anemia: prenatal diagnosis in 30 fetuses at risk.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

19 June 2018

Progressive telomere shortening in aplastic anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 July 2018

Gene therapy of Fanconi anemia: preclinical efficacy using lentiviral vectors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Ethical implications of a new application of preimplantation diagnosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Normal cellular radiosensitivity in an adult Fanconi anaemia patient with marked clinical radiosensitivity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Phenotypic correction of Fanconi anemia group C knockout mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Fine exon-intron structure of the Fanconi anemia group A (FAA) gene and characterization of two genomic deletions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Allogeneic stem cell transplantation for Fanconi Anaemia. Severe Aplastic Anaemia Working Party of the EBMT and EUFAR. European Group for Blood and Marrow Transplantation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Positive diepoxybutane test in only one of two brothers found to be compound heterozygotes for Fanconi's anaemia complementation group C mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Malignancies after marrow transplantation for aplastic anemia and fanconi anemia: a joint Seattle and Paris analysis of results in 700 patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Fanconi anemia diagnosis and the diepoxybutane (DEB) test.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Cancer in relatives of patients with aplastic anemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Fanconi anemia: another disease of unusually high prevalence in the Afrikaans population of South Africa

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735271

28 November 2018

Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Breaks at telomeres and TRF2-independent end fusions in Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

p53-dependent pathway of radio-induced apoptosis is altered in Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal lymphokine production: a novel feature of the genetic disease Fanconi anemia. II. In vitro and in vivo spontaneous overproduction of tumor necrosis factor alpha

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification ofAlu-mediated deletions in the Fanconi anemia geneFAA

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presymptomatic diagnosis of Fanconi's anaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The IVS4 + 4 A to T mutation of the fanconi anemia gene FANCC is not associated with a severe phenotype in Japanese patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A test for Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radiosensitivity in Fanconi's anemia patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparative evaluation of diepoxybutane sensitivity and cell cycle blockage in the diagnosis of Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A test for Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fanconi's Anaemia in the Genetics of Neoplasia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fanconi anemia. Chromosome breakage and cell cycle studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The cell cycle of lymphocytes in Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumor necrosis factor-alpha overproduction in Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Telomere length in myelodysplastic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro effect of cyclophosphamide metabolites on chromosomes of Fanconi anaemia patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fanconi anemia presenting unexpectedly in an adult kindred with no dysmorphic features

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of Fanconi anemia in patients without congenital malformations: An international Fanconi anemia registry study

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Connecting Fanconi anemia to BRCA1

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable response to the diepoxybutane test in two dizygotic twins with Fanconi's anemia and flow cytometry for diagnosis confirmation

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biomedicine. D-Day for BRCA2

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal microsomal detoxification implicated in Fanconi anemia group C by interaction of the FAC protein with NADPH cytochrome P450 reductase

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Involvement of the Fanconi's anemia protein FAC in a pathway that signals to the cyclin B/cdc2 kinase

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of complementation group and mutation type with clinical outcome in fanconi anemia. European Fanconi Anemia Research Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radiosensitivity in Fanconi anaemia: application to the conditioning regimen for bone marrow transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haematopoietic cell transplantation in patients with Fanconi anaemia using alternate donors: results of a total body irradiation dose escalation trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of Fanconi's anaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radiosensitivity in Fanconi anemia: application to the conditioning for bone marrow transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of Brca2 causes genome instability by chromosome breakage and loss associated with centrosome amplification

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apoptosis is not involved in the hypersensitivity of Fanconi anemia cells to mitomycin C

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The fidelity of double strand breaks processing is impaired in complementation groups B and D of Fanconi anemia, a genetic instability syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thrombocytopenia and absent radius (TAR) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased IL-1 beta and TNF alpha secretion in long-term bone marrow culture supernatant from Fanconi's anaemia patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Accelerated telomere shortening and telomerase activation in Fanconi's anaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/12525534

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.40.1.1

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

0 references

Sitelinks

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