(Q41838646)

13 October 2017

Putative RNA-splicing gene LUC7L2 on 7q34 represents a candidate gene in pathogenesis of myeloid malignancies (English)

1 reference

13 October 2017

H Singh

1

1 reference

13 October 2017

A A Lane

2

1 reference

13 October 2017

M Correll

3

1 reference

13 October 2017

B Przychodzen

4

1 reference

13 October 2017

D B Sykes

5

1 reference

13 October 2017

R M Stone

6

1 reference

13 October 2017

K K Ballen

7

1 reference

13 October 2017

P C Amrein

8

1 reference

13 October 2017

J Maciejewski

9

1 reference

13 October 2017

E C Attar

10

1 reference

13 October 2017

24 May 2013

1 reference

13 October 2017

1 reference

13 October 2017

3

1 reference

13 October 2017

e117

1 reference

https://scigraph.springernature.com/pub.10.1038/bcj.2013.16

13 October 2017

0 references

cites work

Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

Clonal architecture of secondary acute myeloid leukemia

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

Frequent pathway mutations of splicing machinery in myelodysplasia

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

Clinical effect of point mutations in myelodysplastic syndromes

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

Recurrent DNMT3A mutations in patients with myelodysplastic syndromes

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

Ribosome defects in disorders of erythropoiesis

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

DNMT3A Mutations in Acute Myeloid Leukemia

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

Recurring mutations found by sequencing an acute myeloid leukemia genome

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674458

Identification of recurring tumor-specific somatic mutations in acute myeloid leukemia by transcriptome sequencing

6 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FBCJ.2013.16

Evidence for a direct role of the disease modifier SCNM1 in splicing

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23708642

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sole abnormalities of chromosome 7 in myeloid malignancies: spectrum, histopathologic correlates, and prognostic implications

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23708642

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/BCJ.2013.16

1 reference

Dimensions Publication ID

13 October 2017

0 references

1 reference

13 October 2017

PubMed publication ID

23708642

1 reference