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T-ALL and thymocytes: a message of noncoding RNAs

Annelynn Wallaert UGent, Kaat Durinck UGent, Tom Taghon UGent, Pieter Van Vlierberghe UGent and Franki Speleman UGent (2017) JOURNAL OF HEMATOLOGY & ONCOLOGY. 10.
abstract
In the last decade, the role for noncoding RNAs in disease was clearly established, starting with microRNAs and later expanded towards long noncoding RNAs. This was also the case for T cell acute lymphoblastic leukemia, which is a malignant blood disorder arising from oncogenic events during normal T cell development in the thymus. By studying the transcriptomic profile of protein-coding genes, several oncogenic events leading to T cell acute lymphoblastic leukemia (T-ALL) could be identified. In recent years, it became apparent that several of these oncogenes function via microRNAs and long noncoding RNAs. In this review, we give a detailed overview of the studies that describe the noncoding RNAome in T-ALL oncogenesis and normal T cell development.
Please use this url to cite or link to this publication:
author
organization
year
type
journalArticle (review)
publication status
published
subject
keyword
T-ALL, Thymocytes, LncRNA, MicroRNA, ACUTE LYMPHOBLASTIC-LEUKEMIA, COMPETING ENDOGENOUS RNA, TUMOR-SUPPRESSOR, CELL DEVELOPMENT, GENE-EXPRESSION, MICRORNA BIOGENESIS, GLUCOCORTICOID-RECEPTOR, MICROPROCESSOR COMPLEX, SIGNATURES DEFINE, MIRNA EXPRESSION
journal title
JOURNAL OF HEMATOLOGY & ONCOLOGY
J. Hematol. Oncol.
volume
10
article number
66
pages
17 pages
Web of Science type
Review
Web of Science id
000396789900001
ISSN
1756-8722
DOI
10.1186/s13045-017-0432-0
language
English
UGent publication?
yes
classification
U
copyright statement
I have transferred the copyright for this publication to the publisher
id
8521064
handle
http://hdl.handle.net/1854/LU-8521064
date created
2017-05-22 12:35:50
date last changed
2017-08-15 20:45:05
@article{8521064,
  abstract     = {In the last decade, the role for noncoding RNAs in disease was clearly established, starting with microRNAs and later expanded towards long noncoding RNAs. This was also the case for T cell acute lymphoblastic leukemia, which is a malignant blood disorder arising from oncogenic events during normal T cell development in the thymus. By studying the transcriptomic profile of protein-coding genes, several oncogenic events leading to T cell acute lymphoblastic leukemia (T-ALL) could be identified. In recent years, it became apparent that several of these oncogenes function via microRNAs and long noncoding RNAs. In this review, we give a detailed overview of the studies that describe the noncoding RNAome in T-ALL oncogenesis and normal T cell development.},
  articleno    = {66},
  author       = {Wallaert, Annelynn and Durinck, Kaat and Taghon, Tom and Van Vlierberghe, Pieter and Speleman, Franki},
  issn         = {1756-8722},
  journal      = {JOURNAL OF HEMATOLOGY \& ONCOLOGY},
  keyword      = {T-ALL,Thymocytes,LncRNA,MicroRNA,ACUTE LYMPHOBLASTIC-LEUKEMIA,COMPETING ENDOGENOUS RNA,TUMOR-SUPPRESSOR,CELL DEVELOPMENT,GENE-EXPRESSION,MICRORNA BIOGENESIS,GLUCOCORTICOID-RECEPTOR,MICROPROCESSOR COMPLEX,SIGNATURES DEFINE,MIRNA EXPRESSION},
  language     = {eng},
  pages        = {17},
  title        = {T-ALL and thymocytes: a message of noncoding RNAs},
  url          = {http://dx.doi.org/10.1186/s13045-017-0432-0},
  volume       = {10},
  year         = {2017},
}

Chicago
Wallaert, Annelynn, Kaat Durinck, Tom Taghon, Pieter Van Vlierberghe, and Franki Speleman. 2017. “T-ALL and Thymocytes: a Message of Noncoding RNAs.” Journal of Hematology & Oncology 10.
APA
Wallaert, A., Durinck, K., Taghon, T., Van Vlierberghe, P., & Speleman, F. (2017). T-ALL and thymocytes: a message of noncoding RNAs. JOURNAL OF HEMATOLOGY & ONCOLOGY, 10.
Vancouver
1.
Wallaert A, Durinck K, Taghon T, Van Vlierberghe P, Speleman F. T-ALL and thymocytes: a message of noncoding RNAs. JOURNAL OF HEMATOLOGY & ONCOLOGY. 2017;10.
MLA
Wallaert, Annelynn, Kaat Durinck, Tom Taghon, et al. “T-ALL and Thymocytes: a Message of Noncoding RNAs.” JOURNAL OF HEMATOLOGY & ONCOLOGY 10 (2017): n. pag. Print.