(Q38487721)

English

Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.

scientific article published on September 2002

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

3 September 2017

Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH. (English)

1 reference

Europe PubMed Central

3 September 2017

0 references

1 reference

based on heuristic

inferred from title

acute myeloid leukemia

1 reference

based on heuristic

inferred from title

1

object named as

Claudia Schoch

1 reference

Europe PubMed Central

3 September 2017

Torsten Haferlach

2

object named as

Torsten Haferlach

1 reference

Europe PubMed Central

3 September 2017

Susanne Schnittger

5

object named as

Susanne Schnittger

1 reference

Europe PubMed Central

3 September 2017

author name string

Sabina Bursch

3

1 reference

Europe PubMed Central

3 September 2017

Daniela Gerstner

4

1 reference

Europe PubMed Central

3 September 2017

Martin Dugas

6

1 reference

Europe PubMed Central

3 September 2017

Wolfgang Kern

7

1 reference

Europe PubMed Central

3 September 2017

Helmut Löffler

8

1 reference

Europe PubMed Central

3 September 2017

Wolfgang Hiddemann

9

1 reference

Europe PubMed Central

3 September 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

1 September 2002

1 reference

Europe PubMed Central

3 September 2017

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

3 September 2017

35

1 reference

Europe PubMed Central

3 September 2017

20-29

1 reference

Europe PubMed Central

3 September 2017

1

1 reference

Europe PubMed Central

3 September 2017

The clinical significance of karyotype in acute myelogenous leukemia.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Prognostic significance of chromosomal abnormalities in acute nonlymphocytic leukemia: a study of 343 patients

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Failure of embryonic hematopoiesis and lethal hemorrhages in mouse embryos heterozygous for a knocked-in leukemia gene CBFB-MYH11.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

p53 mutations in human cancers

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Genetic instabilities in human cancers

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Molecular cloning and chromosomal localization of the human cyclin C (CCNC) and cyclin E (CCNE) genes: deletion of the CCNC gene in human tumors

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Karyotype and age in acute myeloid leukemia. Are they linked?

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Spectral karyotyping in patients with acute myeloid leukemia and a complex karyotype shows hidden aberrations, including recurrent overrepresentation of 21q, 11q, and 22q.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Further characterization of complex chromosomal rearrangements in myeloid malignancies: spectral karyotyping adds precision in defining abnormalities associated with poor prognosis.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Microsatellite instability is not a defining genetic feature of acute myeloid leukemogenesis in adults: results of a retrospective study of 132 patients and review of the literature

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Patients with de novo acute myeloid leukaemia and complex karyotype aberrations show a poor prognosis despite intensive treatment: a study of 90 patients

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Comparison of chromosome banding analysis, interphase- and hypermetaphase-FISH, qualitative and quantitative PCR for diagnosis and for follow-up in chronic myeloid leukemia: a study on 350 cases.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Multicolor Spectral Karyotyping of Human Chromosomes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

The coloring of cytogenetics

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Karyotyping human chromosomes by combinatorial multi-fluor FISH.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Incidence of chromosome abnormalities and clinical significance of karyotype in de novo acute myeloid leukemia.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Retention of wild-type p53 in tumors from p53 heterozygous mice: reduction of p53 dosage can promote cancer formation

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

21 January 2018

Mutations with loss of heterozygosity of p53 are common in therapy-related myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor progno

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytogenetics and their prognostic value in de novo acute myeloid leukaemia: a report on 283 cases

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

A possible correlation between the degree of karyotype aberrations and the rate of sister chromatid exchanges in lymphoma lines

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

Comparison of spectral karyotyping and conventional cytogenetics in 39 patients with acute myeloid leukemia and myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

Screening for MLL tandem duplication in 387 unselected patients with AML identify a prognostically unfavorable subset of AML

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

Dependence of age-specific incidence of acute myeloid leukemia on karyotype

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

Long-term survival in acute myelogenous leukemia: a second follow-up of the Fourth International Workshop on Chromosomes in Leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

High-resolution chromosomes as an independent prognostic indicator in adult acute nonlymphocytic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.10088

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.10088

1 reference

Europe PubMed Central

3 September 2017

1 reference

Europe PubMed Central

3 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q38487721&oldid=1625829940"