Specific molecular mutation patterns delineate chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia (Q43057954)

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scientific article published on 19 September 2014

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English	Specific molecular mutation patterns delineate chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia	scientific article published on 19 September 2014

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scholarly article

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4258749

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13 November 2017

title

Specific molecular mutation patterns delineate chronic neutrophilic leukemia, atypical chronic myeloid leukemia, and chronic myelomonocytic leukemia (English)

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Europe PubMed Central

PMC publication ID

4258749

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13 November 2017

main subject

chronic myeloid leukemia

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leukemia

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based on heuristic

inferred from title

atypical chronic myeloid leukemia

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based on heuristic

inferred from title

chronic neutrophilic leukemia

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based on heuristic

inferred from title

author

Torsten Haferlach

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2

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Torsten Haferlach

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Europe PubMed Central

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13 November 2017

PMC publication ID

4258749

Tamara Alpermann

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Tamara Alpermann

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Europe PubMed Central

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13 November 2017

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4258749

Manja Meggendorfer

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Manja Meggendorfer

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Europe PubMed Central

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13 November 2017

PMC publication ID

4258749

Claudia Haferlach

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Claudia Haferlach

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Europe PubMed Central

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13 November 2017

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4258749

Susanne Schnittger

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Susanne Schnittger

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4258749

author name string

Sabine Jeromin

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4

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4258749

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13 November 2017

Wolfgang Kern

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6

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13 November 2017

publication date

19 September 2014

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Europe PubMed Central

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4258749

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13 November 2017

published in

Haematologica

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13 November 2017

volume

99

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4258749

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13 November 2017

issue

12

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4258749

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13 November 2017

page(s)

e244-6

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4258749

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13 November 2017

cites work

The new genetics of chronic neutrophilic leukemia and atypical CML: implications for diagnosis and treatment

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

26 May 2018

Oncogenic CSF3R mutations in chronic neutrophilic leukemia and atypical CML

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

26 May 2018

CSF3R T618I is a highly prevalent and specific mutation in chronic neutrophilic leukemia.

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

26 May 2018

Recurrent SETBP1 mutations in atypical chronic myeloid leukemia

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

26 May 2018

SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

26 May 2018

Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

26 May 2018

Frequent pathway mutations of splicing machinery in myelodysplasia

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

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26 May 2018

Prognostic significance of ASXL1 mutations in patients with myelodysplastic syndromes

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

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26 May 2018

Prognostic score including gene mutations in chronic myelomonocytic leukemia.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

15 August 2018

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

15 August 2018

Mutations and prognosis in primary myelofibrosis

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

15 August 2018

Molecular basis of myelodysplastic/myeloproliferative neoplasms

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

15 August 2018

Conventional cytogenetics of myeloproliferative diseases other than CML contribute valid information.

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

15 August 2018

Next-Generation Sequencing Technology Reveals a Characteristic Pattern of Molecular Mutations in 72.8% of Chronic Myelomonocytic Leukemia by Detecting Frequent Alterations in TET2, CBL, RAS, and RUNX1

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4258749

retrieved

1 December 2018

Identifiers

DOI

10.3324/HAEMATOL.2014.113159

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stated in

Europe PubMed Central

PMC publication ID

4258749

retrieved

13 November 2017

PMC publication ID

4258749

1 reference

stated in

Europe PubMed Central

PMC publication ID

4258749

retrieved

13 November 2017

PubMed publication ID

25239264

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Europe PubMed Central

PMC publication ID

4258749

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13 November 2017

ResearchGate publication ID

265860126

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