(Q34179542)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23426163%20AND%20SRC:MED&resulttype=core&format=json

24 February 2020

title

Telomere length and telomerase complex mutations in pediatric acute myeloid leukemia (English)

1 reference

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24 February 2020

0 references

1 reference

2

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24 February 2020

author name string

A M Aalbers

1

1 reference

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24 February 2020

N S Young

3

1 reference

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24 February 2020

C M Zwaan

4

1 reference

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24 February 2020

C Wu

5

1 reference

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24 February 2020

S Kajigaya

6

1 reference

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24 February 2020

E A Coenen

7

1 reference

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24 February 2020

A Baruchel

8

1 reference

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24 February 2020

K Geleijns

9

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24 February 2020

V de Haas

10

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24 February 2020

G J L Kaspers

11

1 reference

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24 February 2020

T W Kuijpers

12

1 reference

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24 February 2020

D Reinhardt

13

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24 February 2020

J Trka

14

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24 February 2020

M Zimmermann

15

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24 February 2020

R Pieters

16

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24 February 2020

V H J van der Velden

17

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24 February 2020

M M van den Heuvel-Eibrink

18

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24 February 2020

publication date

21 February 2013

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24 February 2020

1 reference

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24 February 2020

volume

27

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24 February 2020

issue

8

1 reference

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24 February 2020

page(s)

1786-1789

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Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia

24 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4163790

Constitutional telomerase mutations are genetic risk factors for cirrhosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4163790

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4163790

Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4163790

Short telomeres are a risk factor for idiopathic pulmonary fibrosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4163790

Critically short telomeres in acute myeloid leukemia with loss or gain of parts of chromosomes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4163790

Telomeric DNA in normal and leukemic blood cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4163790

Telomerase gene mutations are associated with cirrhosis formation

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FLEU.2013.57

Extensive allelic variation and ultrashort telomeres in senescent human cells.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FLEU.2013.57

The Shortest Telomere, Not Average Telomere Length, Is Critical for Cell Viability and Chromosome Stability

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FLEU.2013.57

Prognostic implications of differences in telomere length between normal and malignant cells from patients with chronic myeloid leukemia measured by flow cytometry.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4163790

Telomere length and hTERT expression in patients with acute myeloid leukemia correlates with chromosomal abnormalities

28 October 2018

1 reference

12 December 2020

Functional characterization of natural telomerase mutations found in patients with hematologic disorders

1 reference

12 December 2020

Short telomeres are associated with genetic complexity, high-risk genomic aberrations, and short survival in chronic lymphocytic leukemia

1 reference

12 December 2020

NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern

1 reference

12 December 2020

Identifiers

DOI

10.1038/LEU.2013.57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23426163%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

24 February 2020

0 references

1 reference

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24 February 2020

PubMed publication ID

23426163

1 reference