(Q35995222)

English

Genetic analysis of patients with leukemic transformation of myeloproliferative neoplasms shows recurrent SRSF2 mutations that are associated with adverse outcome

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Genetic analysis of patients with leukemic transformation of myeloproliferative neoplasms shows recurrent SRSF2 mutations that are associated with adverse outcome (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

1 reference

based on heuristic

inferred from title

10

object named as

Mithat Gönen

0 references

Omar Abdel-Wahab

object named as

Omar Abdel-Wahab

13

0 references

Hagop Kantarjian

11

object named as

Hagop Kantarjian

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Srdan Verstovsek

14

object named as

Srdan Verstovsek

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

12

object named as

Ross L Levine

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

9

object named as

Cyrus Hedvat

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Taghi Manshouri

3

object named as

Taghi Manshouri

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

8

object named as

Adriana Heguy

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

author name string

Su-Jiang Zhang

1

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Raajit Rampal

2

1 reference

Europe PubMed Central

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11 August 2017

Jay Patel

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Nana Mensah

5

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Andrew Kayserian

6

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Todd Hricik

7

1 reference

Europe PubMed Central

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11 August 2017

Mithat Gönen

10

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Europe PubMed Central

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11 August 2017

language of work or name

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publication date

19 March 2012

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Europe PubMed Central

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11 August 2017

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Europe PubMed Central

PMC publication ID

11 August 2017

119

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11 August 2017

19

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11 August 2017

4480-4485

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

IDH mutations in primary myelofibrosis predict leukemic transformation and shortened survival: clinical evidence for leukemogenic collaboration with JAK2V617F

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Frequent pathway mutations of splicing machinery in myelodysplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

DNMT3A Mutations in Acute Myeloid Leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Genomic and biological characterization of exon 4 KRAS mutations in human cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Acquired mutations in the genes encoding IDH1 and IDH2 both are recurrent aberrations in acute myeloid leukemia: prevalence and prognostic value

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

IDH1 and IDH2 gene mutations identify novel molecular subsets within de novo cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Prevalence and prognostic impact of allelic imbalances associated with leukemic transformation of Philadelphia chromosome-negative myeloproliferative neoplasms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Genetic analysis of transforming events that convert chronic myeloproliferative neoplasms to leukemias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Mutations and treatment outcome in cytogenetically normal acute myeloid leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

2 October 2017

Prognostic impact of isocitrate dehydrogenase enzyme isoforms 1 and 2 mutations in acute myeloid leukemia: a study by the Acute Leukemia French Association group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

23 September 2018

IDH1 and IDH2 mutations are frequent genetic alterations in acute myeloid leukemia and confer adverse prognosis in cytogenetically normal acute myeloid leukemia with NPM1 mutation without FLT3 internal tandem duplication

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

23 September 2018

Deletions of the transcription factor Ikaros in myeloproliferative neoplasms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

23 September 2018

Two routes to leukemic transformation after a JAK2 mutation-positive myeloproliferative neoplasm.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

23 September 2018

AML1/RUNX1 point mutation possibly promotes leukemic transformation in myeloproliferative neoplasms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3362363

23 September 2018

p53 lesions in leukemic transformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22431577

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leukemic transformation in myelofibrosis with myeloid metaplasia: a single-institution experience with 91 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/22431577

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myeloproliferative disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/22431577

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mutations of IDH1 and IDH2 in the leukemic transformation of myeloproliferative neoplasms

1 reference

https://pubmed.ncbi.nlm.nih.gov/22431577

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1182/BLOOD-2011-11-390252

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

0 references

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