Terms: = Bone cancer AND PHF6, BORJ, 84295, ENSG00000156531, MGC14797
6 results:
1. Full spectrum of clonal haematopoiesis-driver mutations in chronic heart failure and their associations with mortality.
Kiefer KC; Cremer S; Pardali E; Assmus B; Abou-El-Ardat K; Kirschbaum K; Dorsheimer L; Rasper T; Berkowitsch A; Serve H; Dimmeler S; Zeiher AM; Rieger MA
ESC Heart Fail; 2021 Jun; 8(3):1873-1884. PubMed ID: 33779075
[TBL] [Abstract] [Full Text] [Related]
2. Proteomic Comparison of Malignant Human Germ Cell Tumor Cell Lines.
Bremmer F; Bohnenberger H; Küffer S; Oellerich T; Serve H; Urlaub H; Strauss A; Maatoug Y; Behnes CL; Oing C; Radzun HJ; Ströbel P; Balabanov S; Honecker F
Dis Markers; 2019; 2019():8298524. PubMed ID: 31565104
[TBL] [Abstract] [Full Text] [Related]
3. Clinical, immunophenotypic, and genomic findings of acute undifferentiated leukemia and comparison to acute myeloid leukemia with minimal differentiation: a study from the bone marrow pathology group.
Weinberg OK; Hasserjian RP; Baraban E; Ok CY; Geyer JT; Philip JKSS; Kurzer JH; Rogers HJ; Nardi V; Stone RM; Garcia JS; Hsi ED; Bagg A; Wang SA; Orazi A; Arber DA
Mod Pathol; 2019 Sep; 32(9):1373-1385. PubMed ID: 31000771
[TBL] [Abstract] [Full Text] [Related]
4.
Xiao W; Bharadwaj M; Levine M; Farnhoud N; Pastore F; Getta BM; Hultquist A; Famulare C; Medina JS; Patel MA; Gao Q; Lewis N; Pichardo J; Baik J; Shaffer B; Giralt S; Rampal R; Devlin S; Cimera R; Zhang Y; E Arcila M; Papaemmanuil E; Levine RL; Roshal M
Blood Adv; 2018 Dec; 2(23):3526-3539. PubMed ID: 30530780
[TBL] [Abstract] [Full Text] [Related]
5. Clinical and biological relevance of genetic alterations in pediatric T-cell acute lymphoblastic leukemia in Taiwan.
Yeh TC; Liang DC; Liu HC; Jaing TH; Chen SH; Hou JY; Yang CP; Huang YJ; Yao HW; Huang TY; Lin TH; Shih LY
Pediatr Blood Cancer; 2019 Jan; 66(1):e27496. PubMed ID: 30280491
[TBL] [Abstract] [Full Text] [Related]
6. Detection of an activated JAK3 variant and a Xq26.3 microdeletion causing loss of phf6 and miR-424 expression in myelodysplastic syndromes by combined targeted next generation sequencing and SNP array analysis.
Kunze K; Gamerdinger U; Leßig-Owlanj J; Sorokina M; Brobeil A; Tur MK; Blau W; Burchardt A; Käbisch A; Schliesser G; Kiehl M; Rosenwald A; Rummel M; Grimminger F; Hain T; Chakraborty T; Bräuninger A; Gattenlöhner S
Pathol Res Pract; 2014 Jun; 210(6):369-76. PubMed ID: 24674452
[TBL] [Abstract] [Full Text] [Related]
