571 related articles for article (PubMed ID: 23263491)
21. Targeted sequencing to identify genetic alterations and prognostic markers in pediatric T-cell acute lymphoblastic leukemia.
Chang YH; Yu CH; Jou ST; Lin CY; Lin KH; Lu MY; Wu KH; Chang HH; Lin DT; Lin SW; Chen HY; Yang YL
Sci Rep; 2021 Jan; 11(1):769. PubMed ID: 33436855
[TBL] [Abstract][Full Text] [Related]
22. NKX3.1 is a direct TAL1 target gene that mediates proliferation of TAL1-expressing human T cell acute lymphoblastic leukemia.
Kusy S; Gerby B; Goardon N; Gault N; Ferri F; Gérard D; Armstrong F; Ballerini P; Cayuela JM; Baruchel A; Pflumio F; Roméo PH
J Exp Med; 2010 Sep; 207(10):2141-56. PubMed ID: 20855495
[TBL] [Abstract][Full Text] [Related]
23. The Notch driven long non-coding RNA repertoire in T-cell acute lymphoblastic leukemia.
Durinck K; Wallaert A; Van de Walle I; Van Loocke W; Volders PJ; Vanhauwaert S; Geerdens E; Benoit Y; Van Roy N; Poppe B; Soulier J; Cools J; Mestdagh P; Vandesompele J; Rondou P; Van Vlierberghe P; Taghon T; Speleman F
Haematologica; 2014 Dec; 99(12):1808-16. PubMed ID: 25344525
[TBL] [Abstract][Full Text] [Related]
24. Spectrum of somatic mutations detected by targeted next-generation sequencing and their prognostic significance in adult patients with acute lymphoblastic leukemia.
Feng J; Li Y; Jia Y; Fang Q; Gong X; Dong X; Ru K; Li Q; Zhao X; Liu K; Wang M; Tian Z; Jia Y; Wang Y; Lin D; Wei H; Tang K; Mi Y; Wang J
J Hematol Oncol; 2017 Feb; 10(1):61. PubMed ID: 28245838
[TBL] [Abstract][Full Text] [Related]
25. Oncogenic and Tumor Suppressor Functions for Lymphoid Enhancer Factor 1 in
Carr T; McGregor S; Dias S; Verykokakis M; Le Beau MM; Xue HH; Sigvardsson M; Bartom ET; Kee BL
Front Immunol; 2022; 13():845488. PubMed ID: 35371057
[TBL] [Abstract][Full Text] [Related]
26. The evolution of relapse of adult T cell acute lymphoblastic leukemia.
Sentís I; Gonzalez S; Genescà E; García-Hernández V; Muiños F; Gonzalez C; López-Arribillaga E; Gonzalez J; Fernandez-Ibarrondo L; Mularoni L; Espinosa L; Bellosillo B; Ribera JM; Bigas A; Gonzalez-Perez A; Lopez-Bigas N
Genome Biol; 2020 Nov; 21(1):284. PubMed ID: 33225950
[TBL] [Abstract][Full Text] [Related]
27. Whole exome sequencing hints at a unique mutational profile of paediatric T-cell lymphoblastic lymphoma.
Bonn BR; Huge A; Rohde M; Oschlies I; Klapper W; Voss R; Makarova O; Rossig C; Jürgens H; Seggewiss J; Burkhardt B
Br J Haematol; 2015 Jan; 168(2):308-13. PubMed ID: 25160903
[No Abstract] [Full Text] [Related]
28. The ufmylation modification of ribosomal protein L10 in the development of pancreatic adenocarcinoma.
Wang K; Chen S; Wu Y; Wang Y; Lu Y; Sun Y; Chen Y
Cell Death Dis; 2023 Jun; 14(6):350. PubMed ID: 37280198
[TBL] [Abstract][Full Text] [Related]
29. MAFB enhances oncogenic Notch signaling in T cell acute lymphoblastic leukemia.
Pajcini KV; Xu L; Shao L; Petrovic J; Palasiewicz K; Ohtani Y; Bailis W; Lee C; Wertheim GB; Mani R; Muthusamy N; Li Y; Meijerink JPP; Blacklow SC; Faryabi RB; Cherry S; Pear WS
Sci Signal; 2017 Nov; 10(505):. PubMed ID: 29138297
[TBL] [Abstract][Full Text] [Related]
30. Mutations in the
Collart MA; Kassem S; Villanyi Z
Front Genet; 2017; 8():61. PubMed ID: 28588606
[TBL] [Abstract][Full Text] [Related]
31. RNA sequencing unravels the genetics of refractory/relapsed T-cell acute lymphoblastic leukemia. Prognostic and therapeutic implications.
Gianfelici V; Chiaretti S; Demeyer S; Di Giacomo F; Messina M; La Starza R; Peragine N; Paoloni F; Geerdens E; Pierini V; Elia L; Mancini M; De Propris MS; Apicella V; Gaidano G; Testi AM; Vitale A; Vignetti M; Mecucci C; Guarini A; Cools J; Foà R
Haematologica; 2016 Aug; 101(8):941-50. PubMed ID: 27151993
[TBL] [Abstract][Full Text] [Related]
32. Cost-effective screening of DNMT3A coding sequence identifies somatic mutation in pediatric T-cell acute lymphoblastic leukemia.
Szarzyńska-Zawadzka B; Kosmalska M; Sędek Ł; Sonsala A; Twardoch M; Kowalczyk JR; Szczepański T; Witt M; Dawidowska M
Eur J Haematol; 2017 Dec; 99(6):514-519. PubMed ID: 28905428
[TBL] [Abstract][Full Text] [Related]
33. Mutation and expression analyses of the ribosomal protein gene RPL10 in an extended German sample of patients with autism spectrum disorder.
Chiocchetti A; Pakalapati G; Duketis E; Wiemann S; Poustka A; Poustka F; Klauck SM
Am J Med Genet A; 2011 Jun; 155A(6):1472-5. PubMed ID: 21567917
[No Abstract] [Full Text] [Related]
34. Toward a NOTCH1/FBXW7/RAS/PTEN-based oncogenetic risk classification of adult T-cell acute lymphoblastic leukemia: a Group for Research in Adult Acute Lymphoblastic Leukemia study.
Trinquand A; Tanguy-Schmidt A; Ben Abdelali R; Lambert J; Beldjord K; Lengliné E; De Gunzburg N; Payet-Bornet D; Lhermitte L; Mossafa H; Lhéritier V; Bond J; Huguet F; Buzyn A; Leguay T; Cahn JY; Thomas X; Chalandon Y; Delannoy A; Bonmati C; Maury S; Nadel B; Macintyre E; Ifrah N; Dombret H; Asnafi V
J Clin Oncol; 2013 Dec; 31(34):4333-42. PubMed ID: 24166518
[TBL] [Abstract][Full Text] [Related]
35. New evidence for differential roles of l10 ribosomal proteins from Arabidopsis.
Falcone Ferreyra ML; Casadevall R; Luciani MD; Pezza A; Casati P
Plant Physiol; 2013 Sep; 163(1):378-91. PubMed ID: 23886624
[TBL] [Abstract][Full Text] [Related]
36. Ribosomal protein L10 in mitochondria serves as a regulator for ROS level in pancreatic cancer cells.
Yang J; Chen Z; Liu N; Chen Y
Redox Biol; 2018 Oct; 19():158-165. PubMed ID: 30172100
[TBL] [Abstract][Full Text] [Related]
37. RPL10 mutation segregating in a family with X-linked syndromic Intellectual Disability.
Thevenon J; Michot C; Bole C; Nitschke P; Nizon M; Faivre L; Munnich A; Lyonnet S; Bonnefont JP; Portes VD; Amiel J
Am J Med Genet A; 2015 Aug; 167A(8):1908-12. PubMed ID: 25846674
[TBL] [Abstract][Full Text] [Related]
38. Deleterious point mutations in T-cell acute lymphoblastic leukemia: Mechanistic insights into leukemogenesis.
Roy U; Raghavan SC
Int J Cancer; 2021 Sep; 149(6):1210-1220. PubMed ID: 33634864
[TBL] [Abstract][Full Text] [Related]
39. Oncogenic activation of the Notch1 gene by deletion of its promoter in Ikaros-deficient T-ALL.
Jeannet R; Mastio J; Macias-Garcia A; Oravecz A; Ashworth T; Geimer Le Lay AS; Jost B; Le Gras S; Ghysdael J; Gridley T; Honjo T; Radtke F; Aster JC; Chan S; Kastner P
Blood; 2010 Dec; 116(25):5443-54. PubMed ID: 20829372
[TBL] [Abstract][Full Text] [Related]
40. Whole exome sequencing in the differential diagnosis of Diamond-Blackfan anemia: Clinical and molecular study of three patients with novel RPL5 and mosaic RPS19 mutations.
Errichiello E; Vetro A; Mina T; Wischmeijer A; Berrino E; Carella M; Romagnoli M; Sacchini P; Venesio T; Zecca M; Zuffardi O
Blood Cells Mol Dis; 2017 May; 64():38-44. PubMed ID: 28376382
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
