BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

319 related articles for article (PubMed ID: 25252869)

  • 21. Distinct Patterns of Clonal Evolution Drive Myelodysplastic Syndrome Progression to Secondary Acute Myeloid Leukemia.
    Guess T; Potts CR; Bhat P; Cartailler JA; Brooks A; Holt C; Yenamandra A; Wheeler FC; Savona MR; Cartailler JP; Ferrell PB
    Blood Cancer Discov; 2022 Jul; 3(4):316-329. PubMed ID: 35522837
    [TBL] [Abstract][Full Text] [Related]  

  • 22. RUNX1 mutation associated with clonal evolution in relapsed pediatric acute myeloid leukemia with t(16;21)(p11;q22).
    Ismael O; Shimada A; Elmahdi S; Elshazley M; Muramatsu H; Hama A; Takahashi Y; Yamada M; Yamashita Y; Horide K; Kojima S
    Int J Hematol; 2014 Feb; 99(2):169-74. PubMed ID: 24374719
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clonal architecture of secondary acute myeloid leukemia defined by single-cell sequencing.
    Hughes AE; Magrini V; Demeter R; Miller CA; Fulton R; Fulton LL; Eades WC; Elliott K; Heath S; Westervelt P; Ding L; Conrad DF; White BS; Shao J; Link DC; DiPersio JF; Mardis ER; Wilson RK; Ley TJ; Walter MJ; Graubert TA
    PLoS Genet; 2014 Jul; 10(7):e1004462. PubMed ID: 25010716
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic basis and molecular pathophysiology of classical myeloproliferative neoplasms.
    Vainchenker W; Kralovics R
    Blood; 2017 Feb; 129(6):667-679. PubMed ID: 28028029
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Whole-exome sequencing identifies novel MPL and JAK2 mutations in triple-negative myeloproliferative neoplasms.
    Milosevic Feenstra JD; Nivarthi H; Gisslinger H; Leroy E; Rumi E; Chachoua I; Bagienski K; Kubesova B; Pietra D; Gisslinger B; Milanesi C; Jäger R; Chen D; Berg T; Schalling M; Schuster M; Bock C; Constantinescu SN; Cazzola M; Kralovics R
    Blood; 2016 Jan; 127(3):325-32. PubMed ID: 26423830
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clonal architecture of secondary acute myeloid leukemia.
    Walter MJ; Shen D; Ding L; Shao J; Koboldt DC; Chen K; Larson DE; McLellan MD; Dooling D; Abbott R; Fulton R; Magrini V; Schmidt H; Kalicki-Veizer J; O'Laughlin M; Fan X; Grillot M; Witowski S; Heath S; Frater JL; Eades W; Tomasson M; Westervelt P; DiPersio JF; Link DC; Mardis ER; Ley TJ; Wilson RK; Graubert TA
    N Engl J Med; 2012 Mar; 366(12):1090-8. PubMed ID: 22417201
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical Manifestations and Risk Factors for Complications of Philadelphia Chromosome-Negative Myeloproliferative Neoplasms.
    Duangnapasatit B; Rattarittamrong E; Rattanathammethee T; Hantrakool S; Chai-Adisaksopha C; Tantiworawit A; Norasetthada L
    Asian Pac J Cancer Prev; 2015; 16(12):5013-8. PubMed ID: 26163633
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia.
    Shiba N; Yoshida K; Shiraishi Y; Okuno Y; Yamato G; Hara Y; Nagata Y; Chiba K; Tanaka H; Terui K; Kato M; Park MJ; Ohki K; Shimada A; Takita J; Tomizawa D; Kudo K; Arakawa H; Adachi S; Taga T; Tawa A; Ito E; Horibe K; Sanada M; Miyano S; Ogawa S; Hayashi Y
    Br J Haematol; 2016 Nov; 175(3):476-489. PubMed ID: 27470916
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mass cytometry analysis reveals hyperactive NF Kappa B signaling in myelofibrosis and secondary acute myeloid leukemia.
    Fisher DAC; Malkova O; Engle EK; Miner CA; Fulbright MC; Behbehani GK; Collins TB; Bandyopadhyay S; Zhou A; Nolan GP; Oh ST
    Leukemia; 2017 Sep; 31(9):1962-1974. PubMed ID: 28008177
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Driver mutations and prognosis in primary myelofibrosis: Mayo-Careggi MPN alliance study of 1,095 patients.
    Tefferi A; Nicolosi M; Mudireddy M; Szuber N; Finke CM; Lasho TL; Hanson CA; Ketterling RP; Pardanani A; Gangat N; Mannarelli C; Fanelli T; Guglielmelli P; Vannucchi AM
    Am J Hematol; 2018 Mar; 93(3):348-355. PubMed ID: 29164670
    [TBL] [Abstract][Full Text] [Related]  

  • 31. U2AF1 mutations in primary myelofibrosis are strongly associated with anemia and thrombocytopenia despite clustering with JAK2V617F and normal karyotype.
    Tefferi A; Finke CM; Lasho TL; Wassie EA; Knudson R; Ketterling RP; Hanson CA; Pardanani A
    Leukemia; 2014 Feb; 28(2):431-3. PubMed ID: 24097336
    [No Abstract]   [Full Text] [Related]  

  • 32. Presentation and outcome of patients with 2016 WHO diagnosis of prefibrotic and overt primary myelofibrosis.
    Guglielmelli P; Pacilli A; Rotunno G; Rumi E; Rosti V; Delaini F; Maffioli M; Fanelli T; Pancrazzi A; Pietra D; Salmoiraghi S; Mannarelli C; Franci A; Paoli C; Rambaldi A; Passamonti F; Barosi G; Barbui T; Cazzola M; Vannucchi AM;
    Blood; 2017 Jun; 129(24):3227-3236. PubMed ID: 28351937
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Myeloproliferative neoplasms: Current molecular biology and genetics.
    Saeidi K
    Crit Rev Oncol Hematol; 2016 Feb; 98():375-89. PubMed ID: 26697989
    [TBL] [Abstract][Full Text] [Related]  

  • 34. IDH mutations in primary myelofibrosis predict leukemic transformation and shortened survival: clinical evidence for leukemogenic collaboration with JAK2V617F.
    Tefferi A; Jimma T; Sulai NH; Lasho TL; Finke CM; Knudson RA; McClure RF; Pardanani A
    Leukemia; 2012 Mar; 26(3):475-80. PubMed ID: 21912393
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The Temporal Sequence and the Differences in Somatic Mutation Acquisition Determines Clinical Behaviors of JAK2-Positive Myeloproliferative Neoplasms.
    Byun JM; Song S; Koh Y; Yoon SS; Kim D
    Anticancer Res; 2019 Nov; 39(11):6273-6282. PubMed ID: 31704857
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Primary myelofibrosis: 2013 update on diagnosis, risk-stratification, and management.
    Tefferi A
    Am J Hematol; 2013 Feb; 88(2):141-50. PubMed ID: 23349007
    [TBL] [Abstract][Full Text] [Related]  

  • 37. SRSF2 and U2AF1 mutations in primary myelofibrosis are associated with JAK2 and MPL but not calreticulin mutation and may independently reoccur after allogeneic stem cell transplantation.
    Bartels S; Lehmann U; Büsche G; Schlue J; Mozer M; Stadler J; Triviai I; Alchalby H; Kröger N; Kreipe H
    Leukemia; 2015 Jan; 29(1):253-5. PubMed ID: 25231745
    [No Abstract]   [Full Text] [Related]  

  • 38. Mutations associated with age-related clonal hematopoiesis in PMF patients with rapid progression to myelofibrosis.
    Bartels S; Faisal M; Büsche G; Schlue J; Hasemeier B; Schipper E; Vogtmann J; Westphal L; Lehmann U; Kreipe H
    Leukemia; 2020 May; 34(5):1364-1372. PubMed ID: 31776465
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Two novel NPM1 mutations in an acute myeloid leukemia patient transformed from primary myelofibrosis.
    Park SH; Chi HS; Shim H; Jang S; Park CJ
    Int J Lab Hematol; 2013 Feb; 35(1):e1-3. PubMed ID: 22978565
    [No Abstract]   [Full Text] [Related]  

  • 40. [Clonal evolution of myeloid malignancies].
    Kon A
    Rinsho Ketsueki; 2020; 61(9):1120-1129. PubMed ID: 33162507
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.