(Q36004687)

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Chromosomal aberrations associated with clonal evolution and leukemic transformation in fanconi anemia: clinical and biological implications

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Chromosomal aberrations associated with clonal evolution and leukemic transformation in fanconi anemia: clinical and biological implications (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Heidemarie Neitzel

2

object named as

Heidemarie Neitzel

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

author name string

Stefan Meyer

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Holger Tönnies

3

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

publication date

23 May 2012

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

2012

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

349837

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

copyright license

Creative Commons Attribution 3.0 Unported

1 January 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

Estimation of the prevalence of Fanconi anemia among patients with de novo acute myelogenous leukemia who have poor recovery from chemotherapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Mutations of the SLX4 gene in Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Cytogenetics of childhood acute myeloid leukemia: United Kingdom Medical Research Council Treatment trials AML 10 and 12.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Pathophysiology and management of inherited bone marrow failure syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

EVI1 overexpression in distinct subtypes of pediatric acute myeloid leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Haematopoeitic cell transplantation for Fanconi anaemia - when and how?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Diagnosis of myelodysplastic syndrome among a cohort of 119 patients with fanconi anemia: morphologic and cytogenetic characteristics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Fanconi anemia and its diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

The genetic and molecular basis of Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Inherited susceptibility to common cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Fludarabine-based cytoreductive regimen and T-cell-depleted grafts from alternative donors for the treatment of high-risk patients with Fanconi anaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

TNF-alpha induces leukemic clonal evolution ex vivo in Fanconi anemia group C murine stem cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Fanconi anemia and DNA replication repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Unrelated donor bone marrow transplantation for the treatment of Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Enhanced TNF-alpha-induced apoptosis in Fanconi anemia type C-deficient cells is dependent on apoptosis signal-regulating kinase 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

The Fanconi anaemia gene FANCC promotes homologous recombination and error-prone DNA repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 7.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 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=3366199

2 October 2017

Detection of monosomy 7 in bone marrow by fluorescence in situ hybridization. A study of Fanconi anemia patients and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

DNA cross-linker-induced G2/M arrest in group C Fanconi anemia lymphoblasts reflects normal checkpoint function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Clonal chromosome abnormalities in Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 2017

Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

2 October 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=3366199

2 October 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=3366199

2 October 2017

High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

11 July 2018

Continuous in vivo infusion of interferon-gamma (IFN-gamma) preferentially reduces myeloid progenitor numbers and enhances engraftment of syngeneic wild-type cells in Fancc-/- mice

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

Mutation of the RAD51C gene in a Fanconi anemia-like disorder

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

Spectrum and significance of variants and mutations in the Fanconi anaemia group G gene in children with sporadic acute myeloid leukaemia.

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

Numerical chromosomal changes and risk of development of myelodysplastic syndrome–acute myeloid leukemia in patients with Fanconi anemia

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor.

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

Donor cell-derived acute myeloid leukemia after second allogenic cord blood transplantation in a patient with Fanconi anemia.

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

Deubiquitination of FANCD2 is required for DNA crosslink repair

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

Multiple inhibitory cytokines induce deregulated progenitor growth and apoptosis in hematopoietic cells from Fac-/- mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3366199

23 September 2018

Fanconi anemia (FA)-associated 3q gains in leukemic transformation consistently target EVI1, but do not affect low TERC expression in FA

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

A novel Leu153Ser mutation of the Fanconi anemia FANCD2 gene is associated with severe chemotherapy toxicity in a pediatric T-cell acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1155%2F2012%2F349837

21 January 2018

Chemotherapy for myeloid malignancy in children with Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22675616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MLL-CBP fusion transcript in a therapy-related acute myeloid leukemia with the t(11;16)(q23;p13) which developed in an acute lymphoblastic leukemia patient with Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22675616

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/22675616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High EVI1 expression predicts outcome in younger adult patients with acute myeloid leukemia and is associated with distinct cytogenetic abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/22675616

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/22675616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal studies of leukemic and preleukemic Fanconii's anemia patients: examples of acquired 'chromosomal amplification.'.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22675616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical, molecular, and prognostic significance of WHO type inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q abnormalities in acute myeloid leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22675616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions

1 reference

https://pubmed.ncbi.nlm.nih.gov/22675616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive preleukemia with a chromosomally abnormal clone in a kindred with the Estren-Dameshek variant of Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/22675616

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1155/2012/349837

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

ResearchGate publication ID

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