(Q84888123)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19907438%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

title

DNA copy-number abnormalities do not occur in infant ALL with t(4;11)/MLL-AF4 (English)

1 reference

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12 February 2020

4

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12 February 2020

Grazia Fazio

7

1 reference

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12 February 2020

Giuseppe Basso

9

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12 February 2020

Cristina Battaglia

12

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12 February 2020

author name string

M Bardini

1

1 reference

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12 February 2020

R Spinelli

2

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12 February 2020

S Bungaro

3

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12 February 2020

L Corral

5

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12 February 2020

I Cifola

6

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12 February 2020

M Giordan

8

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12 February 2020

G De Rossi

10

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12 February 2020

A Biondi

11

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12 February 2020

G Cazzaniga

13

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12 February 2020

publication date

12 November 2009

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12 February 2020

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12 February 2020

volume

24

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12 February 2020

issue

1

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12 February 2020

page(s)

169-176

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https://scigraph.springernature.com/pub.10.1038/leu.2009.203

12 February 2020

exact match

0 references

cites work

MLL translocations specify a distinct gene expression profile that distinguishes a unique leukemia

1 reference

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7 January 2021

A treatment protocol for infants younger than 1 year with acute lymphoblastic leukaemia (Interfant-99): an observational study and a multicentre randomised trial.

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7 January 2021

Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements

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7 January 2021

Analysis of prognostic factors of acute lymphoblastic leukemia in infants: report on CCG 1953 from the Children's Oncology Group

1 reference

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7 January 2021

Outcome of risk-based therapy for infant acute lymphoblastic leukemia with or without an MLL gene rearrangement, with emphasis on late effects: a final report of two consecutive studies, MLL96 and MLL98, of the Japan Infant Leukemia Study Group.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

In utero rearrangements in the trithorax-related oncogene in infant leukaemias.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Origins of chromosome translocations in childhood leukaemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

A conditional model of MLL-AF4 B-cell tumourigenesis using invertor technology

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

A murine Mll-AF4 knock-in model results in lymphoid and myeloid deregulation and hematologic malignancy

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

H3K79 methylation profiles define murine and human MLL-AF4 leukemias

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

High-resolution genomic profiling of childhood ALL reveals novel recurrent genetic lesions affecting pathways involved in lymphocyte differentiation and cell cycle progression.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Molecular allelokaryotyping of pediatric acute lymphoblastic leukemias by high-resolution single nucleotide polymorphism oligonucleotide genomic microarray

1 reference

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7 January 2021

Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Mechanisms leading to uniparental disomy and their clinical consequences

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Preferential loss of maternal 9p alleles in childhood acute lymphoblastic leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Long contiguous stretches of homozygosity in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Extended tracts of homozygosity in outbred human populations

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Runs of homozygosity reveal highly penetrant recessive loci in schizophrenia.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Homozygosity haplotype allows a genomewide search for the autosomal segments shared among patients.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Mutations in the SLC34A2 gene are associated with pulmonary alveolar microlithiasis

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

MLL rearrangements in pediatric acute lymphoblastic and myeloblastic leukemias: MLL specific and lineage specific signatures

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Integration of genomic and gene expression data of childhood ALL without known aberrations identifies subgroups with specific genetic hallmarks

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Genomic analysis of the clonal origins of relapsed acute lymphoblastic leukemia.

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Aberrant chromatin at genes encoding stem cell regulators in human mixed-lineage leukemia

1 reference

https://api.crossref.org/works/10.1038%2FLEU.2009.203

7 January 2021

Identifiers

DOI

10.1038/LEU.2009.203

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19907438%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

12 February 2020

0 references

1 reference