Recurrently affected genes in juvenile myelomonocytic leukaemia-Reference-Cited by-同舟云学术

Recurrently affected genes in juvenile myelomonocytic leukaemia

Published:2017-05-09 Issue:1 Volume:182 Page:135-138
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Obenauer Julia C.¹²^ORCID,Kavelaars François G.¹,Sanders Mathijs A.¹,de Vries Andrica C. H.²,de Haas Valerie³,Beverloo H. Berna⁴⁵,De Moerloose Barbara⁶,Lammens Tim⁶,Dworzak Michael⁷,Hoogenboezem Remco M.¹,Valk Peter J. M.¹,Touw Ivo P.¹,van den Heuvel-Eibrink Marry M.²⁸

Affiliation:

1. Department of Haematology; Erasmus University Medical Centre; Rotterdam the Netherlands

2. Department of Paediatric Oncology-Haematology; Erasmus University Medical Centre/Sophia Children's Hospital; Rotterdam the Netherlands

3. Dutch Childhood Oncology Group (DCOG/SKION); The Hague the Netherlands

4. Department of Clinical Genetics; Erasmus University Medical Centre; Rotterdam the Netherlands

5. Dutch Working Group on Haemato-Oncologic Genome Diagnostics; Rotterdam the Netherlands

6. Department of Paediatric Haematology-Oncology and Stem Cell Transplantation; Ghent University Hospital; Ghent Belgium

7. St Anna Children's Hospital and Children's Cancer Research Institute; Department of Paediatrics; Medical University of Vienna; Vienna Austria

8. Princess Màxima Centre for Paediatric Oncology (PMC); Utrecht the Netherlands

Funder

Erasmus Medisch Centrum

Stichting Kinderkanker

Kinderkankerfonds vzw

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.14737/fullpdf

Reference10 articles.

1. Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network;Caye;Nature Genetics,2015

2. Bedside to bench in juvenile myelomonocytic leukemia: insights into leukemogenesis from a rare pediatric leukemia;Chang;Blood,2014

3. Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia;Perez;British Journal of Haematology,2010

4. The function of CUX1 in oxidative DNA damage repair is needed to prevent premature senescence of mouse embryo fibroblasts;Ramdzan;Oncotarget,2015

5. Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia;Sakaguchi;Nature Genetics,2013

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3. Distinctive phenotypes in two children with novel germline RUNX1 mutations - one with myeloid malignancy and increased fetal hemoglobin;Pediatric Hematology and Oncology;2020-09-29

4. iWhale: a computational pipeline based on Docker and SCons for detection and annotation of somatic variants in cancer WES data;Briefings in Bioinformatics;2020-05-20

5. Clinical Impact of Genomic Information in Pediatric Leukemia;Frontiers in Pediatrics;2017-12-14