143 related articles for article (PubMed ID: 26762561)
41. E2F4 functions as a tumour suppressor in acute myeloid leukaemia via inhibition of the MAPK signalling pathway by binding to EZH2.
Feng Y; Li L; Du Y; Peng X; Chen F
J Cell Mol Med; 2020 Feb; 24(3):2157-2168. PubMed ID: 31943751
[TBL] [Abstract][Full Text] [Related]
42. Quantitative proteomic analysis of EZH2 inhibition in acute myeloid leukemia reveals the targets and pathways that precede the induction of cell death.
Sandow JJ; Infusini G; Holik AZ; Brumatti G; Averink TV; Ekert PG; Webb AI
Proteomics Clin Appl; 2017 Sep; 11(9-10):. PubMed ID: 28447382
[TBL] [Abstract][Full Text] [Related]
43.
Stasik S; Middeke JM; Kramer M; Röllig C; Krämer A; Scholl S; Hochhaus A; Crysandt M; Brümmendorf TH; Naumann R; Steffen B; Kunzmann V; Einsele H; Schaich M; Burchert A; Neubauer A; Schäfer-Eckart K; Schliemann C; Krause S; Herbst R; Hänel M; Frickhofen N; Noppeney R; Kaiser U; Baldus CD; Kaufmann M; Rácil Z; Platzbecker U; Berdel WE; Mayer J; Serve H; Müller-Tidow C; Ehninger G; Bornhäuser M; Schetelig J; Thiede C;
Haematologica; 2020 May; 105(5):e228-e231. PubMed ID: 31413097
[No Abstract] [Full Text] [Related]
44. Histone methyltransferase EZH2 epigenetically affects CCNA1 expression in acute myeloid leukemia.
Yang X; Wan M; Yu F; Wu X
Cell Signal; 2021 Nov; 87():110144. PubMed ID: 34509612
[TBL] [Abstract][Full Text] [Related]
45. A novel truncating variant within exon 7 of KAT6B associated with features of both Say-Barber-Bieseker-Young-Simpson syndrome and genitopatellar syndrome: Further evidence of a continuum in the clinical spectrum of KAT6B-related disorders.
Marangi G; Di Giacomo MC; Lattante S; Orteschi D; Patrizi S; Doronzio PN; Riviello FN; Vaisfeld A; Frangella S; Zollino M
Am J Med Genet A; 2018 Feb; 176(2):455-459. PubMed ID: 29226580
[TBL] [Abstract][Full Text] [Related]
46. Excessive growth in a girl with Weaver syndrome.
Ozkan B; Bereket A
J Pediatr Endocrinol Metab; 2000; 13(8):1147-53. PubMed ID: 11085195
[TBL] [Abstract][Full Text] [Related]
47. Higher EZH2 expression is associated with extramedullary infiltration in acute myeloid leukemia.
Zhu Q; Zhang L; Li X; Chen F; Jiang L; Yu G; Wang Z; Yin C; Jiang X; Zhong Q; Zhou H; Ding B; Wang C; Meng F
Tumour Biol; 2016 Aug; 37(8):11409-20. PubMed ID: 27000755
[TBL] [Abstract][Full Text] [Related]
48. [Refractory acute myeloid leukemia developed malignancy-associated hemophagocytic lymphohistiocytosis during treatment of invasive fungal infection].
Yamada A; Moritake H; Sawa D; Shimonodan H; Kojima H; Kamimura S; Nunoi H
Rinsho Ketsueki; 2013 Apr; 54(4):383-7. PubMed ID: 23666221
[TBL] [Abstract][Full Text] [Related]
49. HO-1 promotes resistance to an EZH2 inhibitor through the pRB-E2F pathway: correlation with the progression of myelodysplastic syndrome into acute myeloid leukemia.
He Z; Zhang S; Ma D; Fang Q; Yang L; Shen S; Chen Y; Ren L; Wang J
J Transl Med; 2019 Nov; 17(1):366. PubMed ID: 31711520
[TBL] [Abstract][Full Text] [Related]
50. Novel truncating variants expand the phenotypic spectrum of KAT6B-related disorders.
Brea-Fernández A; Dacruz D; Eirís J; Barros F; Carracedo Á
Am J Med Genet A; 2019 Feb; 179(2):290-294. PubMed ID: 30569622
[TBL] [Abstract][Full Text] [Related]
51. Schinzel-Giedion syndrome in two Brazilian patients: Report of a novel mutation in SETBP1 and literature review of the clinical features.
Carvalho E; Honjo R; Magalhães M; Yamamoto G; Rocha K; Naslavsky M; Zatz M; Passos-Bueno MR; Kim C; Bertola D
Am J Med Genet A; 2015 May; 167A(5):1039-46. PubMed ID: 25663181
[TBL] [Abstract][Full Text] [Related]
52. Clonal shifts in MDS - from SF3B1 to EZH2.
Barbosa Ribeiro A; Coucelo M; Tenreiro R; Simões AT; Marques G; Ribeiro L; Cortesão E; Sarmento-Ribeiro AB
Leuk Lymphoma; 2018 Dec; 59(12):2994-2997. PubMed ID: 29616853
[No Abstract] [Full Text] [Related]
53. Acute myeloid leukemia in Baraitser-Winter cerebrofrontofacial syndrome.
Cianci P; Fazio G; Casagranda S; Spinelli M; Rizzari C; Cazzaniga G; Selicorni A
Am J Med Genet A; 2017 Feb; 173(2):546-549. PubMed ID: 27868373
[TBL] [Abstract][Full Text] [Related]
54. Leukemia cells directly phagocytose blood cells in AML-associated hemophagocytic lymphohistiocytosis: a case report and review of the literature.
Hatano K; Nagai T; Matsuyama T; Sakaguchi Y; Fujiwara S; Oh I; Muroi K; Ozawa K
Acta Haematol; 2015; 133(1):98-100. PubMed ID: 25226795
[No Abstract] [Full Text] [Related]
55. Mutations in the histone methyltransferase Ezh2 drive context-dependent leukemia in Xenopus tropicalis.
Tulkens D; Boelens M; Naert T; Carron M; Demuynck S; Dewaele S; Van Isterdael G; Creytens D; Pieters T; Goossens S; Van Vlierberghe P; Vleminckx K
Leukemia; 2023 Dec; 37(12):2404-2413. PubMed ID: 37794102
[TBL] [Abstract][Full Text] [Related]
56. Novel NLRC4 Mutation Causes a Syndrome of Perinatal Autoinflammation With Hemophagocytic Lymphohistiocytosis, Hepatosplenomegaly, Fetal Thrombotic Vasculopathy, and Congenital Anemia and Ascites.
Liang J; Alfano DN; Squires JE; Riley MM; Parks WT; Kofler J; El-Gharbawy A; Madan-Kheterpal S; Acquaro R; Picarsic J
Pediatr Dev Pathol; 2017; 20(6):498-505. PubMed ID: 28403691
[TBL] [Abstract][Full Text] [Related]
57. Acute myeloid leukemia initially presenting as hemophagocytic lymphohistiocytosis--a case report and review of the literature.
Wang LX; Fei XM; Lu YL; Shi XF; Jiang Q; You HY; Ba R; Zhu Y
Leuk Res; 2010 Jan; 34(1):e46-9. PubMed ID: 19773082
[No Abstract] [Full Text] [Related]
58. Therapy-related acute myeloid leukemia with KMT2A-SNX9 gene fusion associated with a hyperdiploid karyotype after hemophagocytic lymphohistiocytosis.
Sardou-Cezar I; Lopes BA; Andrade FG; Fonseca TCC; Fernandez TS; Larghero P; de Souza RQ; Loth G; Ribeiro LL; Bonfim C; Morgado ES; Marschalek R; Meyer C; Pombo-de-Oliveira MS
Cancer Genet; 2021 Aug; 256-257():86-90. PubMed ID: 34034210
[TBL] [Abstract][Full Text] [Related]
59. A somatic EZH2 mutation in childhood acute myeloid leukemia.
Ernst T; Pflug A; Rinke J; Ernst J; Bierbach U; Beck JF; Hochhaus A; Gruhn B
Leukemia; 2012 Jul; 26(7):1701-3. PubMed ID: 22266912
[No Abstract] [Full Text] [Related]
60. Recommendations for Cancer Surveillance in Individuals with RASopathies and Other Rare Genetic Conditions with Increased Cancer Risk.
Villani A; Greer MC; Kalish JM; Nakagawara A; Nathanson KL; Pajtler KW; Pfister SM; Walsh MF; Wasserman JD; Zelley K; Kratz CP
Clin Cancer Res; 2017 Jun; 23(12):e83-e90. PubMed ID: 28620009
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]