In a multi-institutional cohort of myeloid sarcomas, NFE2 mutation prevalence is lower than previously reported
Blood Adv
.
2021 Dec 14;5(23):5057-5059.
doi: 10.1182/bloodadvances.2021004983.
Authors
Tauangtham Anekpuritanang
1
2
,
Matthew M Klairmont
3
,
Joel Gradowski
3
,
Kohei Hagiwara
4
,
Nathanael G Bailey
5
,
Pranil Chandra
6
,
Yiwei Liu
7
,
Heather L Mulder
4
,
John Easton
4
,
Jinghui Zhang
4
,
Michael G Martin
8
,
Anna B Owczarczyk
9
,
Jennifer B Dunlap
1
,
Guang Fan
1
,
Richard D Press
1
10
,
Philipp W Raess
1
Affiliations
1
Department of Pathology, Oregon Health and Science University, Portland, OR.
2
Department of Pathology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
3
Department of Pathology, University of Tennessee Health Science Center, Memphis, TN.
4
Department of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN.
5
Department of Pathology, University of Pittsburgh School of Medicine and UPMC, Pittsburgh, PA.
6
Genomic and Clinical Pathology, PathGroup, Nashville, TN and.
7
Department of Pharmaceutical Sciences and.
8
Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN.
9
Department of Pathology, University of Michigan, Ann Arbor, MI; and.
10
Knight Cancer Institute, Oregon Health and Science University, Portland, OR.
PMID:
34559205
PMCID:
PMC9152993
DOI:
10.1182/bloodadvances.2021004983
No abstract available
Publication types
Research Support, N.I.H., Extramural
MeSH terms
Cohort Studies
Humans
Mutation*
Prevalence
Sarcoma, Myeloid / diagnosis
Sarcoma, Myeloid / epidemiology
Sarcoma, Myeloid / genetics*