Acquired, nonrandom chromosomal abnormalities associated with the development of acute promyelocytic leukemia in transgenic mice (Q37292292)

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scientific article

Language	Label	Description	Also known as
English	Acquired, nonrandom chromosomal abnormalities associated with the development of acute promyelocytic leukemia in transgenic mice	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Acquired, nonrandom chromosomal abnormalities associated with the development of acute promyelocytic leukemia in transgenic mice (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

1 reference

based on heuristic

inferred from title

acute promyelocytic leukemia

1 reference

based on heuristic

inferred from title

author name string

D B Zimonjic

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

J L Pollock

2

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

P Westervelt

3

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

N C Popescu

4

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

T J Ley

5

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

language of work or name

0 references

publication date

1 November 2000

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

number of pages

6

1 reference

based on heuristic

inferred from page(s)

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

97

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

24

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

13306-13311

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PML regulates p53 acetylation and premature senescence induced by oncogenic Ras

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

A bcr-3 isoform of RARalpha-PML potentiates the development of PML-RARalpha-driven acute promyelocytic leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Genetic disorders associated with cancer predisposition and genomic instability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Genetic diagnosis and molecular monitoring in the management of acute promyelocytic leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Distinct leukemia phenotypes in transgenic mice and different corepressor interactions generated by promyelocytic leukemia variant fusion genes PLZF-RARalpha and NPM-RARalpha

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Deconstructing a disease: RARalpha, its fusion partners, and their roles in the pathogenesis of acute promyelocytic leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

The promyelocytic leukemia gene product (PML) forms stable complexes with the retinoblastoma protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Acute leukemia with promyelocytic features in PML/RARalpha transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

A PMLRARalpha transgene initiates murine acute promyelocytic leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Establishing the presence of the t(15;17) in suspected acute promyelocytic leukaemia: cytogenetic, molecular and PML immunofluorescence assessment of patients entered into the M.R.C. ATRA trial. M.R.C. Adult Leukaemia Working Party

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Multicolor Spectral Karyotyping of Human Chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Characterization of 20q deletions in patients with myeloproliferative disorders or myelodysplastic syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Expression pattern of the RAR alpha-PML fusion gene in acute promyelocytic leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

6 September 2017

Cytogenetics of chronic myelogenous leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

14 September 2017

A role for PML and the nuclear body in genomic stability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

28 September 2017

Immunophenotyping of AML and MDS and detection of residual disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

28 September 2017

Human/mouse homology relationships

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

28 September 2017

Deletions of chromosome 20q and the pathogenesis of myeloproliferative disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

28 September 2017

A distinct tumor suppressor gene locus on chromosome 15q21.1 in sporadic form of colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

26 June 2018

Cloning of the murine homolog of the leukemia-associated PML gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

26 June 2018

Rearrangements in the p53 gene in Philadelphia chromosome positive chronic myelogenous leukemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

26 June 2018

Rearrangement and expression of p53 in the chronic phase and blast crisis of chronic myelogenous leukemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

26 June 2018

Clonal evolution in a myeloid cell line transformed to interleukin-3 independent growth by retroviral transduction and expression of p210bcr/abl

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

26 June 2018

Distinct interactions of PML-RARalpha and PLZF-RARalpha with co-repressors determine differential responses to RA in APL.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

3 September 2018

p53 loss and point mutations are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=27220

3 September 2018

A Detailed Physical and Transcriptional Map of the Region of Chromosome 20 That Is Deleted in Myeloproliferative Disorders and Refinement of the Common Deleted Region

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.97.24.13306

21 January 2018

A sole del(15q) anomaly in post-myelodysplasia acute myeloid leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The flow cytometric pattern of CD34, CD15 and CD13 expression in acute myeloblastic leukemia is highly characteristic of the presence of PML-RARalpha gene rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for early hematopoietic progenitor cell involvement in acute promyelocytic leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The physical map of Mus musculus chromosome 11 reveals evolutionary relationships with different syntenic groups of genes in Homo sapiens

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of acute promyelocytic leukaemia by RT-PCR: detection of PML-RARA and RARA-PML fusion transcripts

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secondary chromosomal abnormalities in acute leukemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the p53 gene mutations in acute myelogenous leukemia: The p53 gene mutations associated with a deletion of chromosome 17

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary vs. secondary neoplasia-associated chromosomal abnormalities--balanced rearrangements vs. genomic imbalances?

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered myeloid development and acute leukemia in transgenic mice expressing PML-RAR alpha under control of cathepsin G regulatory sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secondary cytogenetic changes in acute promyelocytic leukemia--prognostic importance in patients treated with chemotherapy alone and association with the intron 3 breakpoint of the PML gene: a Cancer and Leukemia Group B study

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

RAR alpha1/RAR alpha2-PML mRNA expression in acute promyelocytic leukemia cells: a molecular and laboratory-clinical correlative study

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Refinement of the commonly deleted segment in myeloid leukemias with a del(20q)

1 reference

https://pubmed.ncbi.nlm.nih.gov/11087871

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.97.24.13306

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

2000PNAS...9713306Z

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

0 references

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