(Q33938184)

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Genomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles

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Europe PubMed Central

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30 July 2017

Genomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles (English)

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Europe PubMed Central

PubMed publication ID

30 July 2017

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lymphoblastic leukemia

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author name string

M G Loudin

1

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Europe PubMed Central

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30 July 2017

J Wang

2

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30 July 2017

H-C Eastwood Leung

3

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30 July 2017

S Gurusiddappa

4

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Europe PubMed Central

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30 July 2017

J Meyer

5

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30 July 2017

G Condos

6

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30 July 2017

D Morrison

7

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30 July 2017

A Tsimelzon

8

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30 July 2017

M Devidas

9

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Europe PubMed Central

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30 July 2017

N A Heerema

10

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30 July 2017

A J Carroll

11

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30 July 2017

S E Plon

12

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Europe PubMed Central

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30 July 2017

S P Hunger

13

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Europe PubMed Central

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30 July 2017

G Basso

14

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Europe PubMed Central

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30 July 2017

A Pession

15

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30 July 2017

D Bhojwani

16

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30 July 2017

W L Carroll

17

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30 July 2017

K R Rabin

18

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30 July 2017

publication date

7 June 2011

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30 July 2017

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30 July 2017

25

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30 July 2017

10

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30 July 2017

1555-1563

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Europe PubMed Central

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30 July 2017

Down syndrome childhood acute lymphoblastic leukemia has a unique spectrum of sentinel cytogenetic lesions that influences treatment outcome: a report from the Children's Oncology Group

1 reference

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5 July 2018

Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of IKZF1, Hispanic/Latino ethnicity, and a poor outcome in pediatric B-progenitor acute lymphoblastic leukemia

1 reference

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Leukaemogenesis: more than mutant genes

1 reference

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Functional screening identifies CRLF2 in precursor B-cell acute lymphoblastic leukemia

1 reference

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5 July 2018

Down syndrome acute lymphoblastic leukemia, a highly heterogeneous disease in which aberrant expression of CRLF2 is associated with mutated JAK2: a report from the International BFM Study Group

1 reference

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5 July 2018

Rearrangement of CRLF2 in B-progenitor- and Down syndrome-associated acute lymphoblastic leukemia

1 reference

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Complex human chromosomal and genomic rearrangements

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JAK mutations in high-risk childhood acute lymphoblastic leukemia

1 reference

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Prevalence and clinical correlates of JAK2 mutations in Down syndrome acute lymphoblastic leukaemia.

1 reference

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Metabolism and regulation of canonical histone mRNAs: life without a poly(A) tail

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An integrated genomic analysis of human glioblastoma multiforme

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KEGG for linking genomes to life and the environment

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The complex language of chromatin regulation during transcription

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Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

1 reference

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5 July 2018

Down syndrome and acute lymphoblastic leukaemia

1 reference

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High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

1 reference

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Computational approaches for predicting the biological effect of p53 missense mutations: a comparison of three sequence analysis based methods

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5 July 2018

Structural variation in the human genome

1 reference

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5 July 2018

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles

1 reference

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5 July 2018

Comprehensive statistical study of 452 BRCA1 missense substitutions with classification of eight recurrent substitutions as neutral

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5 July 2018

Systematic discovery of regulatory motifs in human promoters and 3' UTRs by comparison of several mammals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107887

5 July 2018

Origins of chromosome translocations in childhood leukaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107887

5 July 2018

PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107887

5 July 2018

The human and mouse replication-dependent histone genes

1 reference

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Human non-synonymous SNPs: server and survey

1 reference

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Model-based analysis of oligonucleotide arrays: model validation, design issues and standard error application

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Design and analysis of randomized clinical trials requiring prolonged observation of each patient. II. analysis and examples

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5 July 2018

Deregulated expression of cytokine receptor gene, CRLF2, is involved in lymphoid transformation in B-cell precursor acute lymphoblastic leukemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107887

29 October 2018

Specific JAK2 mutation (JAK2R683) and multiple gene deletions in Down syndrome acute lymphoblastic leukemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107887

29 October 2018

Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndrome

1 reference

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29 October 2018

Cytogenetic features of acute lymphoblastic and myeloid leukemias in pediatric patients with Down syndrome: an iBFM-SG study

1 reference

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Whole-genome genotyping with the single-base extension assay

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Presence of the P2RY8-CRLF2 rearrangement is associated with a poor prognosis in non-high-risk precursor B-cell acute lymphoblastic leukemia in children treated according to the ALL-BFM 2000 protocol

1 reference

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12 December 2020

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1 reference

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1 reference

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Polyploid formation in cotton is not accompanied by rapid genomic changes

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2011.128

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based on heuristic

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Identifiers

10.1038/LEU.2011.128

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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