Clinical and molecular relevance of genetic variants in the non-coding transcriptome of patients with cytogenetically normal acute myeloid leukemia.
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Citation:
Haematologica vol 107 (5) 1034-1044
Year:
2022
Type:
Manuscript
Funding:
NCTN
Endpoint:
Secondary-not-in-original
Analysis:
Primary
Data Sharing:
No-Data-Sharing
Status:
Presented/Published
Citation Status:
pub
Note:
Methodological:
No
Biospecimen:
Yes
SDC:
No
Book Volume:
11
Parents:
2784  
Children:
None
Program:
TRP
Primary Committee:
Leuk Corr Sci
Sec. Committees:
   
Pharmas:
 
Grants:
U10CA180821, U10CA180882, , U24CA196171, U10CA180833, U10CA180850, U10CA180861, U10CA180866, U10CA180867, P50CA140158, P30CA16058, R35CA197734, G-509200-004  
Corr. Author:
 
Authors:
                                                     
Networks:
CT063, IL040, LAPS-AL002, LAPS-MA036, LAPS-MO011, LAPS-NY158, LAPS-OH007, NC002, NORTHWELL, OH070   
Study
Multiple Studies, or Legacy Studies in Alliance Study:
CALGB-20202
Phases:
N/A
Keywords:
Adult, Cytosine, Humans, Leukemia, Myeloid, Acute, Middle Aged, Mutation, Prognosis, RNA, Long Noncoding, Thymidine, Transcriptome