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Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

scientific article published in Nature Communications

Claudin 13, a member of the claudin family regulated in mouse stress induced erythropoiesis

artículo científico publicado en 2010

Differences in meiotic recombination rates in childhood acute lymphoblastic leukemia at an MHC class II hotspot close to disease associated haplotypes

artículo científico publicado en 2014

GTF2IRD1 regulates transcription by binding an evolutionarily conserved DNA motif 'GUCE'.

artículo científico publicado en 2007

Genetic variation in the extended major histocompatibility complex and susceptibility to childhood acute lymphoblastic leukemia: a review of the evidence

scientific article published on 12 December 2013

Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia ⬇️

artículo científico publicado en 2018

HLA-DPβ1 Asp84-Lys69 antigen-binding signature predicts event-free survival in childhood B-cell precursor acute lymphoblastic leukaemia: results from the MRC UKALL XI childhood ALL trial.

artículo científico publicado en 2012

Heritable variation at the chromosome 21 gene ERG is associated with acute lymphoblastic leukemia risk in children with and without Down syndrome

scientific article published on 11 July 2019

Inherited genetic susceptibility to acute lymphoblastic leukemia in Down syndrome

scientific article published on 01 October 2019

No association of HLA-A supertype with outcome in childhood acute lymphoblastic leukaemia: results of the UKALL XI trial

scientific article published on 31 January 2011

SNP association mapping across the extended major histocompatibility complex and risk of B-cell precursor acute lymphoblastic leukemia in children

artículo científico publicado en 2013

Strong association of the HLA-DP6 supertype with childhood leukaemia is due to a single allele, DPB1*0601.

artículo científico publicado en 2009

The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A ⬇️

artículo científico publicado en 2015

The human major histocompatibility complex and childhood leukemia: an etiological hypothesis based on molecular mimicry.

scientific article published on 02 December 2008

Transmission of HLA-DP variants from parents to children with B-cell precursor acute lymphoblastic leukemia: Log-linear analysis using the case–parent design

article

Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype

scientific journal article

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