220 related articles for article (PubMed ID: 32632335)
1. Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X.
Liu Y; Li C; Shen S; Chen X; Szlachta K; Edmonson MN; Shao Y; Ma X; Hyle J; Wright S; Ju B; Rusch MC; Liu Y; Li B; Macias M; Tian L; Easton J; Qian M; Yang JJ; Hu S; Look AT; Zhang J
Nat Genet; 2020 Aug; 52(8):811-818. PubMed ID: 32632335
[TBL] [Abstract][Full Text] [Related]
2. Alteration of CTCF-associated chromatin neighborhood inhibits TAL1-driven oncogenic transcription program and leukemogenesis.
Li Y; Liao Z; Luo H; Benyoucef A; Kang Y; Lai Q; Dovat S; Miller B; Chepelev I; Li Y; Zhao K; Brand M; Huang S
Nucleic Acids Res; 2020 Apr; 48(6):3119-3133. PubMed ID: 32086528
[TBL] [Abstract][Full Text] [Related]
3. Noncoding RNA transcription at enhancers and genome folding in cancer.
Isoda T; Morio T; Takagi M
Cancer Sci; 2019 Aug; 110(8):2328-2336. PubMed ID: 31228211
[TBL] [Abstract][Full Text] [Related]
4. Reorganization of the 3D Genome Pinpoints Noncoding Drivers of Primary Prostate Tumors.
Hawley JR; Zhou S; Arlidge C; Grillo G; Kron KJ; Hugh-White R; van der Kwast TH; Fraser M; Boutros PC; Bristow RG; Lupien M
Cancer Res; 2021 Dec; 81(23):5833-5848. PubMed ID: 34642184
[TBL] [Abstract][Full Text] [Related]
5. Noncoding genetic variation in GATA3 increases acute lymphoblastic leukemia risk through local and global changes in chromatin conformation.
Yang H; Zhang H; Luan Y; Liu T; Yang W; Roberts KG; Qian MX; Zhang B; Yang W; Perez-Andreu V; Xu J; Iyyanki S; Kuang D; Stasiak LA; Reshmi SC; Gastier-Foster J; Smith C; Pui CH; Evans WE; Hunger SP; Platanias LC; Relling MV; Mullighan CG; Loh ML; Yue F; Yang JJ
Nat Genet; 2022 Feb; 54(2):170-179. PubMed ID: 35115686
[TBL] [Abstract][Full Text] [Related]
6. Investigation of inherited noncoding genetic variation impacting the pharmacogenomics of childhood acute lymphoblastic leukemia treatment.
Bhattarai KR; Mobley RJ; Barnett KR; Ferguson DC; Hansen BS; Diedrich JD; Bergeron BP; Yoshimura S; Yang W; Crews KR; Manring CS; Jabbour E; Paietta E; Litzow MR; Kornblau SM; Stock W; Inaba H; Jeha S; Pui CH; Cheng C; Pruett-Miller SM; Relling MV; Yang JJ; Evans WE; Savic D
Nat Commun; 2024 May; 15(1):3681. PubMed ID: 38693155
[TBL] [Abstract][Full Text] [Related]
7. 13q12.2 deletions in acute lymphoblastic leukemia lead to upregulation of FLT3 through enhancer hijacking.
Yang M; Safavi S; Woodward EL; Duployez N; Olsson-Arvidsson L; Ungerbäck J; Sigvardsson M; Zaliova M; Zuna J; Fioretos T; Johansson B; Nord KH; Paulsson K
Blood; 2020 Aug; 136(8):946-956. PubMed ID: 32384149
[TBL] [Abstract][Full Text] [Related]
8. Integrated methylome and transcriptome analysis reveals novel regulatory elements in pediatric acute lymphoblastic leukemia.
Almamun M; Levinson BT; van Swaay AC; Johnson NT; McKay SD; Arthur GL; Davis JW; Taylor KH
Epigenetics; 2015; 10(9):882-90. PubMed ID: 26308964
[TBL] [Abstract][Full Text] [Related]
9. Transposable Elements and DNA Methylation Create in Embryonic Stem Cells Human-Specific Regulatory Sequences Associated with Distal Enhancers and Noncoding RNAs.
Glinsky GV
Genome Biol Evol; 2015 May; 7(6):1432-54. PubMed ID: 25956794
[TBL] [Abstract][Full Text] [Related]
10. Aberrant expression of tumor suppressor genes and their association with chimeric oncogenes in pediatric acute lymphoblastic leukemia.
Kustanovich AM; Savitskaja TV; Bydanov OI; Belevtsev MV; Potapnev MP
Leuk Res; 2005 Nov; 29(11):1271-6. PubMed ID: 15878620
[TBL] [Abstract][Full Text] [Related]
11. Genetic and regulatory mechanism of susceptibility to high-hyperdiploid acute lymphoblastic leukaemia at 10p21.2.
Studd JB; Vijayakrishnan J; Yang M; Migliorini G; Paulsson K; Houlston RS
Nat Commun; 2017 Mar; 8():14616. PubMed ID: 28256501
[TBL] [Abstract][Full Text] [Related]
12. The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia.
Liu Y; Easton J; Shao Y; Maciaszek J; Wang Z; Wilkinson MR; McCastlain K; Edmonson M; Pounds SB; Shi L; Zhou X; Ma X; Sioson E; Li Y; Rusch M; Gupta P; Pei D; Cheng C; Smith MA; Auvil JG; Gerhard DS; Relling MV; Winick NJ; Carroll AJ; Heerema NA; Raetz E; Devidas M; Willman CL; Harvey RC; Carroll WL; Dunsmore KP; Winter SS; Wood BL; Sorrentino BP; Downing JR; Loh ML; Hunger SP; Zhang J; Mullighan CG
Nat Genet; 2017 Aug; 49(8):1211-1218. PubMed ID: 28671688
[TBL] [Abstract][Full Text] [Related]
13. Systems Genetics in Human Endothelial Cells Identifies Non-coding Variants Modifying Enhancers, Expression, and Complex Disease Traits.
Stolze LK; Conklin AC; Whalen MB; López Rodríguez M; Õunap K; Selvarajan I; Toropainen A; Örd T; Li J; Eshghi A; Solomon AE; Fang Y; Kaikkonen MU; Romanoski CE
Am J Hum Genet; 2020 Jun; 106(6):748-763. PubMed ID: 32442411
[TBL] [Abstract][Full Text] [Related]
14. Identification of recurrent noncoding mutations in B-cell lymphoma using capture Hi-C.
Cornish AJ; Hoang PH; Dobbins SE; Law PJ; Chubb D; Orlando G; Houlston RS
Blood Adv; 2019 Jan; 3(1):21-32. PubMed ID: 30606723
[TBL] [Abstract][Full Text] [Related]
15. CTCF cooperates with noncoding RNA MYCNOS to promote neuroblastoma progression through facilitating MYCN expression.
Zhao X; Li D; Pu J; Mei H; Yang D; Xiang X; Qu H; Huang K; Zheng L; Tong Q
Oncogene; 2016 Jul; 35(27):3565-76. PubMed ID: 26549029
[TBL] [Abstract][Full Text] [Related]
16. Disease-Associated Single-Nucleotide Polymorphisms From Noncoding Regions in Juvenile Idiopathic Arthritis Are Located Within or Adjacent to Functional Genomic Elements of Human Neutrophils and CD4+ T Cells.
Jiang K; Zhu L; Buck MJ; Chen Y; Carrier B; Liu T; Jarvis JN
Arthritis Rheumatol; 2015 Jul; 67(7):1966-77. PubMed ID: 25833190
[TBL] [Abstract][Full Text] [Related]
17. Transvection-like interchromosomal interaction is not observed at the transcriptional level when tested in the Rosa26 locus in mouse.
Tanimoto K; Matsuzaki H; Okamura E; Ushiki A; Fukamizu A; Engel JD
PLoS One; 2019; 14(2):e0203099. PubMed ID: 30763343
[TBL] [Abstract][Full Text] [Related]
18. Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes.
Spinella JF; Healy J; Saillour V; Richer C; Cassart P; Ouimet M; Sinnett D
BMC Cancer; 2015 Jul; 15():539. PubMed ID: 26201965
[TBL] [Abstract][Full Text] [Related]
19. Genetic validation of whole-transcriptome sequencing for mapping expression affected by cis-regulatory variation.
Babak T; Garrett-Engele P; Armour CD; Raymond CK; Keller MP; Chen R; Rohl CA; Johnson JM; Attie AD; Fraser HB; Schadt EE
BMC Genomics; 2010 Aug; 11():473. PubMed ID: 20707912
[TBL] [Abstract][Full Text] [Related]
20. Mutations in Noncoding
El Ghamrasni S; Quevedo R; Hawley J; Mazrooei P; Hanna Y; Cirlan I; Zhu H; Bruce JP; Oldfield LE; Yang SYC; Guilhamon P; Reimand J; Cescon DW; Done SJ; Lupien M; Pugh TJ
Mol Cancer Res; 2022 Jan; 20(1):102-113. PubMed ID: 34556523
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
