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Journal Abstract Search

182 related items for PubMed ID: 39160538

  • 1.
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  • 2. Clinical and molecular profiling of AML patients with chromosome 7 or 7q deletions in the context of TP53 alterations and venetoclax treatment.
    Abbas HA, Ayoub E, Sun H, Kanagal-Shamanna R, Short NJ, Issa G, Yilmaz M, Pierce S, Rivera D, Cham B, Wing S, Li Z, Hammond D, Jabbour E, Borthakur G, Garcia-Manero G, Andreeff M, Daver N, Kadia T, Konopleva M, DiNardo C, Ravandi F.
    Leuk Lymphoma; 2022 Dec; 63(13):3105-3116. PubMed ID: 36089905
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  • 4. Independent prognostic significance of TP53 mutations in adult acute myeloid leukaemia with complex karyotype.
    Xu N, Lai YY, Chen WM, Jiang H, Wang Y, Wang X, Zhao XS, Huang XJ, Jiang Q, Qin YZ.
    Int J Lab Hematol; 2022 Oct; 44(5):892-899. PubMed ID: 35505580
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  • 5. TP53 mutation in newly diagnosed acute myeloid leukemia and myelodysplastic syndrome.
    Niparuck P, Police P, Noikongdee P, Siriputtanapong K, Limsuwanachot N, Rerkamnuaychoke B, Chuncharunee S, Siriboonpiputtana T.
    Diagn Pathol; 2021 Oct 31; 16(1):100. PubMed ID: 34717674
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  • 6. Monosomal karyotype and chromosome 17p loss or TP53 mutations in decitabine-treated patients with acute myeloid leukemia.
    Becker H, Pfeifer D, Ihorst G, Pantic M, Wehrle J, Rüter BH, Bullinger L, Hackanson B, Germing U, Kuendgen A, Platzbecker U, Döhner K, Ganser A, Hagemeijer A, Wijermans PW, Döhner H, Duyster J, Lübbert M.
    Ann Hematol; 2020 Jul 31; 99(7):1551-1560. PubMed ID: 32504186
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  • 7. Genomic Copy Number Variations in the Myelodysplastic Syndrome and Acute Myeloid Leukemia Patients with del(5q) and/or -7/del(7q).
    Zhang R, Kim YM, Wang X, Li Y, Lu X, Sternenberger AR, Li S, Lee JY.
    Int J Med Sci; 2015 Jul 31; 12(9):719-26. PubMed ID: 26392809
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  • 8. Clinical impact of KMT2C and SPRY4 expression levels in intensively treated younger adult acute myeloid leukemia patients.
    Kayser S, Feszler M, Krzykalla J, Schick M, Kramer M, Benner A, Thol F, Platzbecker U, Müller-Tidow C, Ho AD, Ehninger G, Heuser M, Schlenk RF, Thiede C, Röllig C, Krämer A.
    Eur J Haematol; 2017 Dec 31; 99(6):544-552. PubMed ID: 28940816
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  • 9. Acute myeloid leukemia or myelodysplastic syndrome with chromosome 17 abnormalities and long-term outcomes with or without hematopoietic stem cell transplantation.
    Britt A, Mohyuddin GR, McClune B, Singh A, Lin T, Ganguly S, Abhyankar S, Shune L, McGuirk J, Skikne B, Godwin A, Pessetto Z, Golem S, Divine C, Dias A.
    Leuk Res; 2020 Aug 31; 95():106402. PubMed ID: 32590108
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  • 10. RAS, FLT3, and TP53 mutations in therapy-related myeloid malignancies with abnormalities of chromosomes 5 and 7.
    Side LE, Curtiss NP, Teel K, Kratz C, Wang PW, Larson RA, Le Beau MM, Shannon KM.
    Genes Chromosomes Cancer; 2004 Mar 31; 39(3):217-23. PubMed ID: 14732923
    [Abstract] [Full Text] [Related]

  • 11. Gene mutation patterns in patients with minimally differentiated acute myeloid leukemia.
    Kao HW, Liang DC, Wu JH, Kuo MC, Wang PN, Yang CP, Shih YS, Lin TH, Huang YH, Shih LY.
    Neoplasia; 2014 Jun 31; 16(6):481-8. PubMed ID: 25022553
    [Abstract] [Full Text] [Related]

  • 12. The Clinical impact of PTPN11 mutations in adults with acute myeloid leukemia.
    Alfayez M, Issa GC, Patel KP, Wang F, Wang X, Short NJ, Cortes JE, Kadia T, Ravandi F, Pierce S, Assi R, Garcia-Manero G, DiNardo CD, Daver N, Pemmaraju N, Kantarjian H, Borthakur G.
    Leukemia; 2021 Mar 31; 35(3):691-700. PubMed ID: 32561839
    [Abstract] [Full Text] [Related]

  • 13. Acute myeloid leukemia with del(9q) is characterized by frequent mutations of NPM1, DNMT3A, WT1 and low expression of TLE4.
    Herold T, Metzeler KH, Vosberg S, Hartmann L, Jurinovic V, Opatz S, Konstandin NP, Schneider S, Zellmeier E, Ksienzyk B, Graf A, Krebs S, Blum H, Cristina Sauerland M, Büchner T, Berdel WE, Wörmann BJ, Mansmann U, Hiddemann W, Bohlander SK, Spiekermann K, Greif PA.
    Genes Chromosomes Cancer; 2017 Jan 31; 56(1):75-86. PubMed ID: 27636548
    [Abstract] [Full Text] [Related]

  • 14. Impact of PTPN11 mutations on clinical outcome analyzed in 1529 patients with acute myeloid leukemia.
    Stasik S, Eckardt JN, 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, Middeke JM, Thiede C, Study Alliance Leukemia (SAL).
    Blood Adv; 2021 Sep 14; 5(17):3279-3289. PubMed ID: 34459887
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  • 17. Chromosomal aberrations in 17p predict in vitro drug resistance and short overall survival in acute myeloid leukemia.
    Nahi H, Lehmann S, Bengtzen S, Jansson M, Möllgård L, Paul C, Merup M.
    Leuk Lymphoma; 2008 Mar 14; 49(3):508-16. PubMed ID: 18297528
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  • 18. Secondary genetic lesions in acute myeloid leukemia with inv(16) or t(16;16): a study of the German-Austrian AML Study Group (AMLSG).
    Paschka P, Du J, Schlenk RF, Gaidzik VI, Bullinger L, Corbacioglu A, Späth D, Kayser S, Schlegelberger B, Krauter J, Ganser A, Köhne CH, Held G, von Lilienfeld-Toal M, Kirchen H, Rummel M, Götze K, Horst HA, Ringhoffer M, Lübbert M, Wattad M, Salih HR, Kündgen A, Döhner H, Döhner K.
    Blood; 2013 Jan 03; 121(1):170-7. PubMed ID: 23115274
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