| 1 |
32431543 |
10.2147/CMAR.S242903 |
2022 |
Clinicopathological Characteristics and Mutational Profiling of Adult T-Cell Lymphoblastic Lymphoma in a Chinese Population. |
PHF6 |
| 2 |
32821125 |
10.2147/OTT.S258365 |
2022 |
<i>SET-CAN</i> Fusion Gene in Acute Leukemia and Myeloid Neoplasms: Report of Three Cases and a Literature Review. |
PHF6 |
| 3 |
34440292 |
10.3390/genes12081118 |
2022 |
T-Cell Acute Lymphoblastic Leukemia: Biomarkers and Their Clinical Usefulness. |
PHF6 |
| 4 |
34465864 |
10.1038/s41375-021-01392-1 |
2022 |
PHF6 and JAK3 mutations cooperate to drive T-cell acute lymphoblastic leukemia progression. |
PHF6 |
| 5 |
35253299 |
10.1002/gcc.23036 |
2022 |
CRLF2 overexpression defines an immature-like subgroup which is rescued through restoration of the PRC2 function in T-cell precursor acute lymphoblastic leukemia. |
PHF6 |
| 6 |
35685993 |
10.21147/j.issn.1000-9604.2022.02.03 |
2022 |
Genomic landscape of T-cell lymphoblastic lymphoma. |
PHF6 |
| 7 |
35734596 |
10.3389/fonc.2022.846573 |
2022 |
The Clinical Characteristics and Prognosis of AYA and Older Adult ETP-ALL/LBL: A Real-World Multicenter Study in China. |
PHF6 |
| 8 |
36000950 |
10.1002/pbc.29926 |
2022 |
Diverse mutations and structural variations contribute to Notch signaling deregulation in paediatric T-cell lymphoblastic lymphoma. |
PHF6 |
| 9 |
36008597 |
10.1007/s12015-022-10447-4 |
2022 |
The Role of PHF6 in Hematopoiesis and Hematologic Malignancies. |
PHF6 |
| 10 |
33095873 |
10.1182/bloodadvances.2019001307 |
2021 |
Landscape of driver mutations and their clinical impacts in pediatric B-cell precursor acute lymphoblastic leukemia. |
PHF6 |
| 11 |
33436855 |
10.1038/s41598-020-80613-6 |
2021 |
Targeted sequencing to identify genetic alterations and prognostic markers in pediatric T-cell acute lymphoblastic leukemia. |
PHF6 |
| 12 |
33578108 |
10.1016/j.jbior.2021.100788 |
2021 |
Mutations that collaborate with IL-7Ra signaling pathways to drive ALL. |
PHF6 |
| 13 |
33634864 |
10.1002/ijc.33527 |
2021 |
Deleterious point mutations in T-cell acute lymphoblastic leukemia: Mechanistic insights into leukemogenesis. |
PHF6 |
| 14 |
30171027 |
10.3324/haematol.2017.186320 |
2020 |
Clinical and molecular characteristics of <i>MEF2D</i> fusion-positive B-cell precursor acute lymphoblastic leukemia in childhood, including a novel translocation resulting in <i>MEF2D-HNRNPH1</i> gene fusion. |
PHF6 |
| 15 |
30567843 |
10.1158/2159-8290.CD-18-1005 |
2020 |
<i>Phf6</i> Loss Enhances HSC Self-Renewal Driving Tumor Initiation and Leukemia Stem Cell Activity in T-ALL. |
PHF6 |
| 16 |
30810217 |
10.1111/bjh.15812 |
2020 |
Phenotype switch in acute lymphoblastic leukaemia associated with 3 years of persistent CAR T cell directed-CD19 selective pressure. |
PHF6 |
| 17 |
31270080 |
10.1182/bloodadvances.2018028993 |
2020 |
Clinical and biological features of PTPN2-deleted adult and pediatric T-cell acute lymphoblastic leukemia. |
PHF6 |
| 18 |
31992840 |
10.1038/s41375-019-0685-4 |
2020 |
Adult T-cell acute lymphoblastic leukemias with IL7R pathway mutations are slow-responders who do not benefit from allogeneic stem-cell transplantation. |
PHF6 |
| 19 |
32164600 |
10.1186/s12885-020-6709-7 |
2020 |
Genetic mutational analysis of pediatric acute lymphoblastic leukemia from a single center in China using exon sequencing. |
PHF6 |
| 20 |
33283700 |
10.19746/j.cnki.issn.1009-2137.2020.06.001 |
2020 |
[Gene Mutation in Acute Lymphoblastic Leukemia by DNA Sequencing]. |
PHF6 |
| 21 |
30117174 |
10.1002/ajh.25256 |
2019 |
Genomic and clinical characterization of B/T mixed phenotype acute leukemia reveals recurrent features and T-ALL like mutations. |
PHF6 |
| 22 |
30209976 |
10.1080/15384101.2018.1522912 |
2019 |
PTPN14 regulates Roquin2 stability by tyrosine dephosphorylation. |
PHF6 |
| 23 |
30280491 |
10.1002/pbc.27496 |
2019 |
Clinical and biological relevance of genetic alterations in pediatric T-cell acute lymphoblastic leukemia in Taiwan. |
PHF6 |
| 24 |
30551478 |
10.1016/j.biopha.2018.11.083 |
2019 |
The depletion of PHF6 decreases the drug sensitivity of T-cell acute lymphoblastic leukemia to prednisolone. |
PHF6 |
| 25 |
30635552 |
10.1038/s12276-018-0195-x |
2019 |
CDKN2B downregulation and other genetic characteristics in T-acute lymphoblastic leukemia. |
PHF6 |
| 26 |
27602765 |
10.18632/oncotarget.11796 |
2018 |
Genomic characterization of pediatric T-cell acute lymphoblastic leukemia reveals novel recurrent driver mutations. |
PHF6 |
| 27 |
27874290 |
10.1080/10428194.2016.1260124 |
2018 |
Impact of clinical factors on outcome of leukemia patients with TLS-ERG fusion gene. |
PHF6 |
| 28 |
28747286 |
10.4274/tjh.2017.0194 |
2018 |
Coexistence of EZH2, NOTCH1, IL7R, and PHF6 Mutations in Adult T-cell Acute Lymphoblastic Leukemia. |
PHF6 |
| 29 |
30111389 |
10.7534/j.issn.1009-2137.2018.04.001 |
2018 |
[Study on Immunophenotypes and Gene of Acute Lymphoblastic Leukemia]. |
PHF6 |
| 30 |
27531766 |
10.7534/j.issn.1009-2137.2016.04.010 |
2017 |
[Mutation of IL-7R in Adult Patients with T-cell Acute Lymphoblastic Leukemia and Its Clinical Significance]. |
PHF6 |
| 31 |
28607179 |
10.1101/gad.295857.117 |
2017 |
PHF6 regulates phenotypic plasticity through chromatin organization within lineage-specific genes. |
PHF6 |
| 32 |
26206799 |
10.3324/haematol.2015.130179 |
2016 |
Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia. |
PHF6 |
| 33 |
24710217 |
10.1038/ncomms4630 |
2015 |
The landscape of somatic mutations in epigenetic regulators across 1,000 paediatric cancer genomes. |
PHF6 |
| 34 |
24895337 |
10.3324/haematol.2013.099515 |
2015 |
MicroRNA-128-3p is a novel oncomiR targeting PHF6 in T-cell acute lymphoblastic leukemia. |
PHF6 |
| 35 |
25595890 |
10.18632/oncotarget.2218 |
2015 |
Mutational spectrum of adult T-ALL. |
PHF6 |
| 36 |
25601084 |
10.1074/jbc.M114.610196 |
2015 |
Structural basis of plant homeodomain finger 6 (PHF6) recognition by the retinoblastoma binding protein 4 (RBBP4) component of the nucleosome remodeling and deacetylase (NuRD) complex. |
PHF6 |
| 37 |
26341754 |
10.1007/s00277-015-2474-0 |
2015 |
Genetic mutational profiling analysis of T cell acute lymphoblastic leukemia reveal mutant FBXW7 as a prognostic indicator for inferior survival. |
PHF6 |
| 38 |
24554700 |
10.1074/jbc.M113.535351 |
2014 |
Structural and functional insights into the human Börjeson-Forssman-Lehmann syndrome-associated protein PHF6. |
PHF6 |
| 39 |
22928734 |
10.3109/10428194.2012.725203 |
2013 |
Somatic mutations of PHF6 in patients with chronic myeloid leukemia in blast crisis. |
PHF6 |
| 40 |
23114116 |
|
2013 |
[Expression of SET-NUP214 fusion gene in patients with T-cell acute lymphoblastic leukemia and its clinical significance]. |
PHF6 |
| 41 |
23341344 |
10.1002/gcc.22039 |
2013 |
The molecular profile of adult T-cell acute lymphoblastic leukemia: mutations in RUNX1 and DNMT3A are associated with poor prognosis in T-ALL. |
PHF6 |
| 42 |
23354995 |
10.1007/s00277-012-1664-2 |
2013 |
Gene mutation profiles and prognostic implications in Korean patients with T-lymphoblastic leukemia. |
PHF6 |
| 43 |
21736506 |
10.3109/0284186X.2011.592148 |
2012 |
Somatic mutation of PHF6 gene in T-cell acute lymphoblatic leukemia, acute myelogenous leukemia and hepatocellular carcinoma. |
PHF6 |
| 44 |
21880637 |
10.3324/haematol.2011.043083 |
2012 |
Mutations of PHF6 are associated with mutations of NOTCH1, JAK1 and rearrangement of SET-NUP214 in T-cell acute lymphoblastic leukemia. |
PHF6 |
| 45 |
22675565 |
10.1371/journal.pone.0038463 |
2012 |
High accuracy mutation detection in leukemia on a selected panel of cancer genes. |
PHF6 |
| 46 |
21642990 |
10.1038/ng.858 |
2011 |
A cooperative microRNA-tumor suppressor gene network in acute T-cell lymphoblastic leukemia (T-ALL). |
PHF6 |
| 47 |
20228800 |
10.1038/ng.542 |
2010 |
PHF6 mutations in T-cell acute lymphoblastic leukemia. |
PHF6 |
| 48 |
20589626 |
10.1002/pbc.22661 |
2010 |
PHF6 mutations in T-lineage acute lymphoblastic leukemia. |
PHF6 |
| 49 |
20806366 |
10.1002/pbc.22574 |
2010 |
T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6. |
PHF6 |
Datasets
Models
