These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

92 related articles for article (PubMed ID: 8808725)

  • 1. Monosomy 7 myeloproliferative disease associated with neurofibromatosis type I: a case report.
    Savasan S; Zülfikar B; Ozgeneci A; Ozbek U; Sengün Z
    J Chemother; 1996 Jun; 8(3):243-6. PubMed ID: 8808725
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Hereditary hematopoietic malignancy with emphasis of juvenile chronic myelogenous leukemia and 7 monosomy syndrome].
    Hayashi Y
    Nihon Rinsho; 1995 Nov; 53(11):2737-41. PubMed ID: 8538036
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Monosomy 7 myelodysplastic syndrome and other second malignant neoplasms in children with neurofibromatosis type 1.
    Maris JM; Wiersma SR; Mahgoub N; Thompson P; Geyer RJ; Hurwitz CG; Lange BJ; Shannon KM
    Cancer; 1997 Apr; 79(7):1438-46. PubMed ID: 9083167
    [TBL] [Abstract][Full Text] [Related]  

  • 4. p53 mutation as the second event in juvenile chronic myelogenous leukemia in a patient with neurofibromatosis type 1.
    Luria D; Avigad S; Cohen IJ; Stark B; Weitz R; Zaizov R
    Cancer; 1997 Nov; 80(10):2013-8. PubMed ID: 9366306
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders.
    Shannon KM; O'Connell P; Martin GA; Paderanga D; Olson K; Dinndorf P; McCormick F
    N Engl J Med; 1994 Mar; 330(9):597-601. PubMed ID: 8302341
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Monosomy 7 myeloproliferative disease in children with neurofibromatosis, type 1: epidemiology and molecular analysis.
    Shannon KM; Watterson J; Johnson P; O'Connell P; Lange B; Shah N; Steinherz P; Kan YW; Priest JR
    Blood; 1992 Mar; 79(5):1311-8. PubMed ID: 1536955
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosome pattern in juvenile chronic myelogenous leukemia, myelodysplastic syndrome, and acute leukemia associated with neurofibromatosis.
    Kaneko Y; Maseki N; Sakurai M; Shibuya A; Shinohara T; Fujimoto T; Kanno H; Nishikawa A
    Leukemia; 1989 Jan; 3(1):36-41. PubMed ID: 2491896
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Childhood myeloproliferative disorders.
    Cotter FE
    Baillieres Clin Haematol; 1998 Dec; 11(4):875-98. PubMed ID: 10640222
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Juvenile chronic myelogenous leukemia, neurofibromatosis 1, and xanthoma.
    Jang KA; Choi JH; Sung KJ; Moon KC; Koh JK; Im DJ
    J Dermatol; 1999 Jan; 26(1):33-5. PubMed ID: 10063210
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular evidence that childhood monosomy 7 syndrome is distinct from juvenile chronic myelogenous leukemia and other childhood myeloproliferative disorders.
    Butcher M; Frenck R; Emperor J; Paderanga D; Maybee D; Olson K; Shannon K
    Genes Chromosomes Cancer; 1995 Jan; 12(1):50-7. PubMed ID: 7534111
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic analysis is consistent with the hypothesis that NF1 limits myeloid cell growth through p21ras.
    Kalra R; Paderanga DC; Olson K; Shannon KM
    Blood; 1994 Nov; 84(10):3435-9. PubMed ID: 7949098
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of neurofibromatosis type 1 gene mutation in juvenile chronic myelogenous leukemia.
    Watanabe I; Horiuchi T; Hatta N; Matsumoto M; Koike K; Kojima S; Ohga S; Fujita S
    Acta Haematol; 1998; 100(1):22-5. PubMed ID: 9691142
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lymphoid blast crisis of B-lineage phenotype with monosomy 7 in a patient with juvenile chronic myelogenous leukemia (JCML).
    Lau RC; Squire J; Brisson L; Kamel-Reid S; Grunberger T; Dubé I; Letarte M; Shannon K; Freedman MH
    Leukemia; 1994 May; 8(5):903-8. PubMed ID: 8182949
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Detection of trisomy 8 and monosomy 7 in chronic granulocytic leukemia and myelodysplastic syndrome by cytogenetic analysis and fluorescence in situ hybridization].
    Szabó Gabriella P; Balogh E; Jakab Z; Germán P; Bodnár F; Kiss A; Telek B; Oláh E
    Orv Hetil; 2002 Dec; 143(50):2775-9. PubMed ID: 12583317
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Nf1 deficiency causes Ras-mediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia.
    Largaespada DA; Brannan CI; Jenkins NA; Copeland NG
    Nat Genet; 1996 Feb; 12(2):137-43. PubMed ID: 8563750
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Monosomy 7 with severe myelodysplasia developing during imatinib treatment of Philadelphia-positive chronic myeloid leukemia: two cases with a different outcome.
    Navarro JT; Feliu E; Grau J; Espinet B; Colomer D; Ribera JM; Oriol A; Granada I; Juncà J; Millá F
    Am J Hematol; 2007 Sep; 82(9):849-51. PubMed ID: 17563075
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Loss of heterozygosity of NF1 gene in juvenile chronic myelogenous leukemia with neurofibromatosis type 1.
    Kai S; Sumita H; Fujioka K; Takahashi H; Hanzawa N; Funabiki T; Ikuta K; Sasaki H
    Int J Hematol; 1998 Jul; 68(1):53-60. PubMed ID: 9713168
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Myelodysplastic syndromes: the pediatric point of view.
    Locatelli F; Zecca M; Pession A; Maserati E; De Stefano P; Severi F
    Haematologica; 1995; 80(3):268-79. PubMed ID: 7672722
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inherited predispositions and hyperactive Ras in myeloid leukemogenesis.
    Lauchle JO; Braun BS; Loh ML; Shannon K
    Pediatr Blood Cancer; 2006 May; 46(5):579-85. PubMed ID: 16261595
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Juvenile xanthogranuloma, neurofibromatosis, and juvenile chronic myelogenous leukemia. World statistical analysis.
    Zvulunov A; Barak Y; Metzker A
    Arch Dermatol; 1995 Aug; 131(8):904-8. PubMed ID: 7632061
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.