Spliceosome mutations in myelodysplastic syndromes and chronic myelomonocytic leukemia. (Q38074757)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23327988%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

review article

2 references

28 November 2023

Spliceosome mutations in myelodysplastic syndromes and chronic myelomonocytic leukemia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23327988%20AND%20SRC:MED&resulttype=core&format=json

chronic myelomonocytic leukemia

22 February 2020

main subject

1 reference

6 November 2020

myelodysplastic syndrome

1 reference

6 November 2020

1 reference

8 September 2019

1 reference

12 October 2019

1 reference

6 November 2020

1

1 reference

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22 February 2020

Olivier Kosmider

2

1 reference

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22 February 2020

Raphael A Itzykson

4

1 reference

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22 February 2020

Olivier Bernard

5

1 reference

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22 February 2020

Eric Solary

6

1 reference

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22 February 2020

Michaela Fontenay

7

1 reference

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22 February 2020

author name string

Frederik Damm

3

1 reference

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22 February 2020

language of work or name

English

0 references

publication date

1 November 2012

10 references

6 March 2019

3 April 2019

20 June 2019

30 June 2019

8 September 2019

14 September 2019

12 October 2019

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22 February 2020

6 November 2020

28 November 2023

10 references

6 March 2019

3 April 2019

20 June 2019

30 June 2019

8 September 2019

14 September 2019

12 October 2019

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22 February 2020

6 November 2020

28 November 2023

3

1 reference

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22 February 2020

issue

11

1 reference

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22 February 2020

page(s)

1284-1293

1 reference

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Creative Commons Attribution 2.5 Generic

22 February 2020

copyright license

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6 March 2019

3 April 2019

20 June 2019

30 June 2019

8 September 2019

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on focus list of Wikimedia project

28 November 2023

ScienceSource

0 references

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Spliceosomal gene mutations are frequent events in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemia

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

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Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia

6 September 2017

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Recurrent mutations in the U2AF1 splicing factor in myelodysplastic syndromes

6 September 2017

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SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value

6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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6 September 2017

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HnRNP proteins controlled by c-Myc deregulate pyruvate kinase mRNA splicing in cancer

14 September 2017

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The biflavonoid isoginkgetin is a general inhibitor of Pre-mRNA splicing

14 September 2017

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14 September 2017

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14 September 2017

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SR proteins function in coupling RNAP II transcription to pre-mRNA splicing.

14 September 2017

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14 September 2017

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Prognostic score including gene mutations in chronic myelomonocytic leukemia.

28 September 2017

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Clinical importance of SF3B1 mutations in Chinese with myelodysplastic syndromes with ring sideroblasts

31 August 2018

1 reference

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Mutations affecting mRNA splicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3717792

XUTs are a class of Xrn1-sensitive antisense regulatory non-coding RNA in yeast.

31 August 2018

1 reference

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Clonal architecture of chronic myelomonocytic leukemias

31 August 2018

1 reference

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SF3B1 mutations in myelodysplastic syndromes: clinical associations and prognostic implications

3 December 2018

1 reference

12 December 2020

Genetic Interactions in Cancer Progression and Treatment

1 reference

12 December 2020

SF3B1 mutations in primary myelofibrosis: clinical, histopathology and genetic correlates among 155 patients

1 reference

12 December 2020

A Pre-mRNA degradation pathway that selectively targets intron-containing genes requires the nuclear poly(A)-binding protein

1 reference

12 December 2020

The clinical implication of SRSF2 mutation in patients with myelodysplastic syndrome and its stability during disease evolution

1 reference

12 December 2020

SRSF2 mutations in primary myelofibrosis: significant clustering with IDH mutations and independent association with inferior overall and leukemia-free survival

1 reference

12 December 2020

SF3B1, a splicing factor is frequently mutated in refractory anemia with ring sideroblasts

1 reference

12 December 2020

Spliceosomal gene aberrations are rare, coexist with oncogenic mutations, and are unlikely to exert a driver effect in childhood MDS and JMML

1 reference

12 December 2020

Identifiers

DOI

10.18632/ONCOTARGET.749

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23327988%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23327988%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

PubMed publication ID

23327988

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23327988%20AND%20SRC:MED&resulttype=core&format=json