(Q33397876)

English

Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53.

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53. (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

based on heuristic

inferred from title

Rashmi Kanagal-shamanna

object named as

Rashmi Kanagal-Shamanna

1

0 references

Guillermo Garcia-Manero

6

object named as

Guillermo Garcia-Manero

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

L Jeffrey Medeiros

9

object named as

L Jeffrey Medeiros

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

author name string

Carlos E Bueso-Ramos

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Bedia Barkoh

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Gary Lu

4

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Sa Wang

5

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Saroj Vadhan-Raj

7

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Daniela Hoehn

8

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

C Cameron Yin

10

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

language of work or name

0 references

publication date

28 October 2011

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

118

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

2879-2888

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Chromosome patterns in 26 South African children with acute nonlymphocytic leukemia (ANLL).

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Isochromosome 17q in a case of myelofibrosis with myeloid metaplasia terminating in blastic transformation.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Isochromosome (17q) in Ph-negative chronic myelocytic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Analysis of the p53 gene in patients with isochromosome 17q and Ph1-positive or -negative myeloid leukemia.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Cytogenetic abnormalities in a series of 1,029 patients with primary myelodysplastic syndromes: a report from the US with a focus on some undefined single chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Quantification of fibrosis and osteosclerosis in myeloproliferative neoplasms: a computer-assisted image study.

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

HDM4 is overexpressed in mantle cell lymphoma and its inhibition induces p21 expression and apoptosis

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Cuplike nuclei (prominent nuclear invaginations) in acute myeloid leukemia are highly associated with FLT3 internal tandem duplication and NPM1 mutation

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Prevalence and prognostic significance of Flt3 internal tandem duplication in pediatric acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Localization of the human G-CSF gene to the region of a breakpoint in the translocation typical of acute promyelocytic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Focus on acute leukemias

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Isochromosome 17q as a sole anomaly: A distinct myelodysplastic syndrome entity?

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

21 January 2018

Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinical course

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome studies in preleukemic states. IV. Myeloproliferative versus cytopenic disorders

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

Isochromosome 17 in a patient with a myeloproliferative disorders terminating in eosinophilic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

Karyotype analysis in acute nonlymphocytic leukemia (ANLL): comparison with ethnic group, age, morphology, and survival

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

Isochromosome 17q in a patient with acute myeloblastic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

GCSF gene is expressed but not rearranged in a patient with isochromosome 17q positive acute nonlymphocytic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

Refractory anemia with ring sideroblasts associated with i(17q) and mutation of the TP53 gene

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

Isochromosome i(17q) as a sole cytogenetic abnormality in a case of leukemic transformation from myelodysplastic syndrome (MDS)/myeloproliferative diseases (MPD)

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

Isochromosome 17q in Ph-negative chronic myelocytic leukemia

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

Distinct patterns of cytogenetic and clinical progression in chronic myeloproliferative neoplasms with or without JAK2 or MPL mutations

1 reference

https://api.crossref.org/works/10.1002%2FCNCR.26537

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/CNCR.26537

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

ResearchGate publication ID

0 references

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=Q33397876&oldid=2183758009"