BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

369 related articles for article (PubMed ID: 8431915)

  • 21. The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
    Maserati E; Pressato B; Valli R; Minelli A; Sainati L; Patitucci F; Marletta C; Mastronuzzi A; Poli F; Lo Curto F; Locatelli F; Danesino C; Pasquali F
    Br J Haematol; 2009 Apr; 145(2):190-7. PubMed ID: 19222471
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Karyotype evolution in the bone marrow of a patient with Fanconi anemia: breakpoints in clonal anomalies of this disease.
    Huret JL; Tanzer J; Guilhot F; Frocrain-Herchkovitch C; Savage JR
    Cytogenet Cell Genet; 1988; 48(4):224-7. PubMed ID: 3248378
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Does monosomy 5 really exist in myelodysplastic syndromes and acute myeloid leukemia?
    Galván AB; Mallo M; Arenillas L; Salido M; Espinet B; Pedro C; Florensa L; Serrano S; Solé F
    Leuk Res; 2010 Sep; 34(9):1242-5. PubMed ID: 20362335
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 5q- anomaly preceding acute myeloblastic leukemia with 53 chromosomes without chromosome 5 abnormality.
    Jonveaux P; Daniel MT; Berger R
    Cancer Genet Cytogenet; 1993 Oct; 70(2):146-7. PubMed ID: 8242598
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Trisomy 4 and ring chromosome in a patient with acute myelomonocytic leukemia.
    Vicari L; Sebastio L; Stanziola MC; Fasanaro A; Ferrara F
    Haematologica; 1994; 79(1):83-5. PubMed ID: 15378955
    [TBL] [Abstract][Full Text] [Related]  

  • 26. t(1;7) in acute myeloblastic leukemia following myelodysplastic syndrome (RAEB-T).
    Defferrari R; Sessarego M; Santini G; Ajmar F
    Tumori; 1988 Oct; 74(5):555-8. PubMed ID: 3217990
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Coexistent t(8;21)(q22;q22) Translocation and 5q Deletion in Acute Myeloid Leukemia.
    Yamamoto K; Yakushijin K; Sanada Y; Kawamoto S; Matsuoka H; Minami H
    J Clin Exp Hematop; 2015; 55(3):181-5. PubMed ID: 26763368
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Cytogenetic abnormalities in 532 patients with myeloid leukemias and myelodyplastic syndrome. The Czechoslovak MDS Cooperative Group.
    Michalová K; Musilová J; Zemanová Z
    Czech Med; 1990; 13(4):133-44. PubMed ID: 2081440
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Chromosomal loss and deletion are the most common mechanisms for loss of heterozygosity from chromosomes 5 and 7 in malignant myeloid disorders.
    Neuman WL; Rubin CM; Rios RB; Larson RA; Le Beau MM; Rowley JD; Vardiman JW; Schwartz JL; Farber RA
    Blood; 1992 Mar; 79(6):1501-10. PubMed ID: 1347709
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Occupational history and involvement of chromosomes 5 and 7 in acute nonlymphocytic leukemia.
    Narod SA; Dubé ID
    Cancer Genet Cytogenet; 1989 Apr; 38(2):261-9. PubMed ID: 2655887
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Aberrations of chromosome 5 in myeloid malignancies with complex chromosome abnormalities].
    Liu Q; Xu W; Zhu Y; Fan L; Qiu HR; Wang R; Qiao C; Li JY
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2008 Dec; 16(6):1257-60. PubMed ID: 19099622
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Concurrent pernicious anemia and myelodysplastic syndrome.
    Drabick JJ; Davis BJ; Byrd JC
    Ann Hematol; 2001 Apr; 80(4):243-5. PubMed ID: 11401093
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An abnormal clone with monosomy 7 and trisomy 21 in the bone marrow of a child with congenital agranulocytosis (Kostmann disease) treated with granulocyte colony-stimulating factor. Evolution towards myelodysplastic syndrome and acute basophilic leukemia.
    Shekhter-Levin S; Penchansky L; Wollman MR; Sherer ME; Wald N; Gollin SM
    Cancer Genet Cytogenet; 1995 Oct; 84(2):99-104. PubMed ID: 8536230
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Childhood myelodysplastic syndrome.
    Chatterjee T; Choudhry VP
    Indian J Pediatr; 2013 Sep; 80(9):764-71. PubMed ID: 23912822
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Myelodysplastic syndrome associated with monosomy 7 in a child with Bloom syndrome.
    Aktas D; Koc A; Boduroglu K; Hicsonmez G; Tuncbilek E
    Cancer Genet Cytogenet; 2000 Jan; 116(1):44-6. PubMed ID: 10616531
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genetic disruption of both Fancc and Fancg in mice recapitulates the hematopoietic manifestations of Fanconi anemia.
    Pulliam-Leath AC; Ciccone SL; Nalepa G; Li X; Si Y; Miravalle L; Smith D; Yuan J; Li J; Anur P; Orazi A; Vance GH; Yang FC; Hanenberg H; Bagby GC; Clapp DW
    Blood; 2010 Oct; 116(16):2915-20. PubMed ID: 20606166
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Fluctuation of a clone 46,XX,i(7q) in bone marrow in a Fanconi anaemia.
    Huret JL; Benz E; Guilhot F; Brizard A; Tanzer J
    Hum Genet; 1986 Sep; 74(1):98-100. PubMed ID: 3759089
    [TBL] [Abstract][Full Text] [Related]  

  • 38. AML-associated cytogenetic abnormalities (inv (16), del (16), t(8;21)) in patients with myelodysplastic syndromes.
    Estey E; Trujillo JM; Cork A; O'Brien S; Beran M; Kantarjian H; Keating M; Freireich EJ; Stass S
    Hematol Pathol; 1992; 6(1):43-8. PubMed ID: 1601822
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
    Zhu Y; Xu W; Liu Q; Pan J; Qiu H; Wang R; Qiao C; Jiang Y; Zhang S; Fan L; Zhang J; Shen Y; Xue Y; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):579-82. PubMed ID: 18841577
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel der(1)t(1;19) in two patients with myeloid neoplasias.
    Tchinda J; Volpert S; Neumann T; Kennerknecht I; Ritter J; Büchner T; Berdel WE; Horst J
    Cancer Genet Cytogenet; 2002 Feb; 133(1):61-5. PubMed ID: 11890991
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.