(Q36270713)

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Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Concomitant analysis of EZH2 and ASXL1 mutations in myelofibrosis, chronic myelomonocytic leukemia and blast-phase myeloproliferative neoplasms (English)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

1 reference

based on heuristic

inferred from title

chronic myelomonocytic leukemia

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

10

object named as

A Tefferi

1 reference

Europe PubMed Central

13 August 2017

PMC publication ID

author name string

O Abdel-Wahab

1

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

A Pardanani

2

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

J Patel

3

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

M Wadleigh

4

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

T Lasho

5

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

A Heguy

6

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

M Beran

7

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

D G Gilliland

8

1 reference

Europe PubMed Central

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13 August 2017

R L Levine

9

1 reference

Europe PubMed Central

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13 August 2017

publication date

1 April 2011

1 reference

Europe PubMed Central

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13 August 2017

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

25

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Europe PubMed Central

PMC publication ID

13 August 2017

7

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

1200-1202

1 reference

Europe PubMed Central

PMC publication ID

13 August 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=4641450

30 September 2017

Spectrum of mutations in RARS-T patients includes TET2 and ASXL1 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4641450

29 June 2018

Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4641450

22 September 2018

Dynamic International Prognostic Scoring System (DIPSS) predicts progression to acute myeloid leukemia in primary myelofibrosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4641450

22 September 2018

Mutual exclusion of ASXL1 and NPM1 mutations in a series of acute myeloid leukemias.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4641450

22 September 2018

Mutations of ASXL1 gene in myeloproliferative neoplasms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4641450

22 September 2018

ASXL1 mutation is associated with poor prognosis and acute transformation in chronic myelomonocytic leukaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21455215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression

1 reference

https://pubmed.ncbi.nlm.nih.gov/21455215

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/LEU.2011.58

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

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