BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 33368842)

  • 1. Sister chromatid cohesion defects are associated with chromosomal copy number heterogeneity in high hyperdiploid childhood acute lymphoblastic leukemia.
    Moura-Castro LH; Peña-Martínez P; Castor A; Galeev R; Larsson J; Järås M; Yang M; Paulsson K
    Genes Chromosomes Cancer; 2021 Jun; 60(6):410-417. PubMed ID: 33368842
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Proteogenomics and Hi-C reveal transcriptional dysregulation in high hyperdiploid childhood acute lymphoblastic leukemia.
    Yang M; Vesterlund M; Siavelis I; Moura-Castro LH; Castor A; Fioretos T; Jafari R; Lilljebjörn H; Odom DT; Olsson L; Ravi N; Woodward EL; Harewood L; Lehtiö J; Paulsson K
    Nat Commun; 2019 Apr; 10(1):1519. PubMed ID: 30944321
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sister chromatid cohesion defects are associated with chromosome instability in Hodgkin lymphoma cells.
    Sajesh BV; Lichtensztejn Z; McManus KJ
    BMC Cancer; 2013 Aug; 13():391. PubMed ID: 23962039
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clonal origin and development of high hyperdiploidy in childhood acute lymphoblastic leukaemia.
    Woodward EL; Yang M; Moura-Castro LH; van den Bos H; Gunnarsson R; Olsson-Arvidsson L; Spierings DCJ; Castor A; Duployez N; Zaliova M; Zuna J; Johansson B; Foijer F; Paulsson K
    Nat Commun; 2023 Mar; 14(1):1658. PubMed ID: 36966135
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Sequential and hierarchical chromosomal changes and chromosome instability are distinct features of high hyperdiploid pediatric acute lymphoblastic leukemia.
    Alpár D; Pajor G; Varga P; Kajtár B; Pótó L; Mátics R; Vojcek A; Ottoffy G; Szuhai K; Pajor L
    Pediatr Blood Cancer; 2014 Dec; 61(12):2208-14. PubMed ID: 25174722
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia.
    Gutierrez-Camino A; Richer C; St-Onge P; Lopez-Lopez E; Bañeres AC; de Andoin NG; Sastre A; Astigarraga I; Martin-Guerrero I; Sinnett D; Garcia-Orad A
    Epigenomics; 2020 Nov; 12(22):1949-1955. PubMed ID: 33245684
    [No Abstract]   [Full Text] [Related]  

  • 7. A matter of choice: the establishment of sister chromatid cohesion.
    Uhlmann F
    EMBO Rep; 2009 Oct; 10(10):1095-102. PubMed ID: 19745840
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Impaired condensin complex and Aurora B kinase underlie mitotic and chromosomal defects in hyperdiploid B-cell ALL.
    Molina O; Vinyoles M; Granada I; Roca-Ho H; Gutierrez-Agüera F; Valledor L; López-López CM; Rodríguez-González P; Trincado JL; Menéndez ST; Pal D; Ballerini P; den Boer ML; Plensa I; Mar Perez-Iribarne M; Rodríguez-Perales S; Calasanz MJ; Ramírez-Orellana M; Rodríguez R; Camós M; Calvo M; Bueno C; Menéndez P
    Blood; 2020 Jul; 136(3):313-327. PubMed ID: 32321174
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel phenotypes observed in patients with
    Karastaneva A; Nebral K; Schlagenhauf A; Baschin M; Palankar R; Juch H; Heitzer E; Speicher MR; Höfler G; Grigorow I; Urban C; Benesch M; Greinacher A; Haas OA; Seidel MG
    J Med Genet; 2020 Jun; 57(6):427-433. PubMed ID: 31704777
    [No Abstract]   [Full Text] [Related]  

  • 10. The cohesin-interacting protein, precocious dissociation of sisters 5A/sister chromatid cohesion protein 112, is up-regulated in human astrocytic tumors.
    Hagemann C; Weigelin B; Schommer S; Schulze M; Al-Jomah N; Anacker J; Gerngras S; Kühnel S; Kessler AF; Polat B; Ernestus RI; Patel R; Vince GH
    Int J Mol Med; 2011 Jan; 27(1):39-51. PubMed ID: 21069257
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prognostic impact of RUNX1 and ETV6 gene copy number on pediatric B-cell precursor acute lymphoblastic leukemia with or without hyperdiploidy.
    Kutlay NY; Pekpak E; Altıner S; Ileri T; Vicdan AN; Dinçaslan H; Ince EU; Tukun FA
    Int J Hematol; 2016 Sep; 104(3):368-77. PubMed ID: 27393278
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cohesin gene defects may impair sister chromatid alignment and genome stability in Arabidopsis thaliana.
    Schubert V; Weissleder A; Ali H; Fuchs J; Lermontova I; Meister A; Schubert I
    Chromosoma; 2009 Oct; 118(5):591-605. PubMed ID: 19533160
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Investigating the Interplay between Sister Chromatid Cohesion and Homolog Pairing in Drosophila Nuclei.
    Senaratne TN; Joyce EF; Nguyen SC; Wu CT
    PLoS Genet; 2016 Aug; 12(8):e1006169. PubMed ID: 27541002
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copy number genome alterations are associated with treatment response and outcome in relapsed childhood ETV6/RUNX1-positive acute lymphoblastic leukemia.
    Bokemeyer A; Eckert C; Meyr F; Koerner G; von Stackelberg A; Ullmann R; Türkmen S; Henze G; Seeger K
    Haematologica; 2014 Apr; 99(4):706-14. PubMed ID: 24241490
    [TBL] [Abstract][Full Text] [Related]  

  • 15. AtCTF7 is required for establishment of sister chromatid cohesion and association of cohesin with chromatin during meiosis in Arabidopsis.
    Singh DK; Andreuzza S; Panoli AP; Siddiqi I
    BMC Plant Biol; 2013 Aug; 13():117. PubMed ID: 23941555
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ETV6/RUNX1-positive childhood acute lymphoblastic leukemia (ALL): The spectrum of clonal heterogeneity and its impact on prognosis.
    Ampatzidou M; Papadhimitriou SI; Paterakis G; Pavlidis D; Tsitsikas Κ; Kostopoulos IV; Papadakis V; Vassilopoulos G; Polychronopoulou S
    Cancer Genet; 2018 Aug; 224-225():1-11. PubMed ID: 29778230
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clonal heterogeneity and rates of specific chromosome gains are risk predictors in childhood high-hyperdiploid B-cell acute lymphoblastic leukemia.
    Ramos-Muntada M; Trincado JL; Blanco J; Bueno C; Rodríguez-Cortez VC; Bataller A; López-Millán B; Schwab C; Ortega M; Velasco P; Blanco ML; Nomdedeu J; Ramírez-Orellana M; Minguela A; Fuster JL; Cuatrecasas E; Camós M; Ballerini P; Escherich G; Boer J; DenBoer M; Hernández-Rivas JM; Calasanz MJ; Cazzaniga G; Harrison CJ; Menéndez P; Molina O
    Mol Oncol; 2022 Aug; 16(16):2899-2919. PubMed ID: 35726693
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Defects in the Fanconi Anemia Pathway and Chromatid Cohesion in Head and Neck Cancer.
    Stoepker C; Ameziane N; van der Lelij P; Kooi IE; Oostra AB; Rooimans MA; van Mil SE; Brink A; Dietrich R; Balk JA; Ylstra B; Joenje H; Feller SM; Brakenhoff RH
    Cancer Res; 2015 Sep; 75(17):3543-53. PubMed ID: 26122845
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers.
    Barber TD; McManus K; Yuen KW; Reis M; Parmigiani G; Shen D; Barrett I; Nouhi Y; Spencer F; Markowitz S; Velculescu VE; Kinzler KW; Vogelstein B; Lengauer C; Hieter P
    Proc Natl Acad Sci U S A; 2008 Mar; 105(9):3443-8. PubMed ID: 18299561
    [TBL] [Abstract][Full Text] [Related]  

  • 20. RAG1 co-expression signature identifies ETV6-RUNX1-like B-cell precursor acute lymphoblastic leukemia in children.
    Chen D; Camponeschi A; Nordlund J; Marincevic-Zuniga Y; Abrahamsson J; Lönnerholm G; Fogelstrand L; Mårtensson IL
    Cancer Med; 2021 Jun; 10(12):3997-4003. PubMed ID: 33987955
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.