Excess congenital non-synonymous variation in leukemia-associated genes in MLL− infant leukemia: a Children’s Oncology Group report
Published 2013 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Excess congenital non-synonymous variation in leukemia-associated genes in MLL− infant leukemia: a Children’s Oncology Group report
Authors
Keywords
-
Journal
LEUKEMIA
Volume 28, Issue 6, Pages 1235-1241
Publisher
Springer Nature
Online
2013-12-04
DOI
10.1038/leu.2013.367
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- FLT3 activation cooperates with MLL-AF4 fusion protein to abrogate the hematopoietic specification of human ESCs
- (2013) C. Bueno et al. BLOOD
- Exome sequencing identifies an MLL3 gene germ line mutation in a pedigree of colorectal cancer and acute myeloid leukemia
- (2013) W.-D. Li et al. BLOOD
- Identification of somatic and germline mutations using whole exome sequencing of congenital acute lymphoblastic leukemia
- (2013) Vivian Y Chang et al. BMC CANCER
- Cancer Genome Landscapes
- (2013) B. Vogelstein et al. SCIENCE
- Commonly altered genomic regions in acute myeloid leukemia are enriched for somatic mutations involved in chromatin remodeling and splicing
- (2012) A. Dolnik et al. BLOOD
- Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing
- (2012) Enrique Ramos et al. BMC GENOMICS
- Familial history of cancer and leukemia in children younger than 2 years of age in Brazil
- (2012) Arnaldo C. Couto et al. EUROPEAN JOURNAL OF CANCER PREVENTION
- Common genetic variation contributes significantly to the risk of childhood B-cell precursor acute lymphoblastic leukemia
- (2012) V Enciso-Mora et al. LEUKEMIA
- De novo mutations in human genetic disease
- (2012) Joris A. Veltman et al. NATURE REVIEWS GENETICS
- Genetic variants modify susceptibility to leukemia in infants: A Children's Oncology Group report
- (2012) Julie A. Ross et al. PEDIATRIC BLOOD & CANCER
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- (2012) J. A. Tennessen et al. SCIENCE
- Enforced expression of MLL-AF4 fusion in cord blood CD34+ cells enhances the hematopoietic repopulating cell function and clonogenic potential but is not sufficient to initiate leukemia
- (2011) R. Montes et al. BLOOD
- Clan Genomics and the Complex Architecture of Human Disease
- (2011) James R. Lupski et al. CELL
- The AF4{middle dot}MLL fusion protein is capable of inducing ALL in mice without requirement of MLL{middle dot}AF4
- (2010) A. Bursen et al. BLOOD
- Vascular anastomoses leading to amelia and cutis aplasia in a dizygotic twin pregnancy
- (2010) Mary C Phelan et al. CLINICAL GENETICS
- Rare genetic variants and the risk of cancer
- (2010) Walter Bodmer et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Mixed lineage leukemia: roles in gene expression, hormone signaling and mRNA processing
- (2010) Khairul I. Ansari et al. FEBS Journal
- TWIN-TWIN TRANSFUSION SYNDROME IN A DICHORIONIC-MONOZYGOTIC TWIN PREGNANCY: The End of a Paradigm?
- (2010) Ruben Quintero et al. Fetal and Pediatric Pathology
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- The Sequence Alignment/Map format and SAMtools
- (2009) H. Li et al. BIOINFORMATICS
- Discordance of MLL-rearranged (MLL-R) infant acute lymphoblastic leukemia in monozygotic twins with spontaneous clearance of preleukemic clone in unaffected twin
- (2009) M. K. Chuk et al. BLOOD
- Gene expression profiling-based dissection of MLL translocated and MLL germline acute lymphoblastic leukemia in infants
- (2009) R. W. Stam et al. BLOOD
- Childhood and adolescent cancer survival in the US by race and ethnicity for the diagnostic period 1975-1999
- (2008) Amy M. Linabery et al. CANCER
- Common and rare variants in multifactorial susceptibility to common diseases
- (2008) Walter Bodmer et al. NATURE GENETICS
- Data and Theory Point to Mainly Additive Genetic Variance for Complex Traits
- (2008) William G. Hill et al. PLoS Genetics
- Trends in childhood cancer incidence in the U.S. (1992–2004)
- (2007) Amy M. Linabery et al. CANCER
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started