BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 2562922)

  • 1. Chromosome 7 long arm deletion in myeloid disorders: a narrow breakpoint region in 7q22 defined by molecular mapping.
    Kere J; Ruutu T; Davies KA; Roninson IB; Watkins PC; Winqvist R; de la Chapelle A
    Blood; 1989 Jan; 73(1):230-4. PubMed ID: 2562922
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias.
    Fischer K; Fröhling S; Scherer SW; McAllister Brown J; Scholl C; Stilgenbauer S; Tsui LC; Lichter P; Döhner H
    Blood; 1997 Mar; 89(6):2036-41. PubMed ID: 9058725
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromosome 7 long arm deletion breakpoints in preleukemia: mapping by pulsed field gel electrophoresis.
    Kere J
    Nucleic Acids Res; 1989 Feb; 17(4):1511-20. PubMed ID: 2922284
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Plasminogen activator inhibitor type 1 gene is located at region q21.3-q22 of chromosome 7 and genetically linked with cystic fibrosis.
    Klinger KW; Winqvist R; Riccio A; Andreasen PA; Sartorio R; Nielsen LS; Stuart N; Stanislovitis P; Watkins P; Douglas R
    Proc Natl Acad Sci U S A; 1987 Dec; 84(23):8548-52. PubMed ID: 2891140
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular characterization of chromosome 7 long arm deletions in myeloid disorders.
    Kere J; Ruutu T; Lahtinen R; de la Chapelle A
    Blood; 1987 Nov; 70(5):1349-53. PubMed ID: 2889483
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular characterization of the 7q deletion in myeloid disorders.
    Lewis S; Abrahamson G; Boultwood J; Fidler C; Potter A; Wainscoat JS
    Br J Haematol; 1996 Apr; 93(1):75-80. PubMed ID: 8611479
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial bone marrow monosomy 7. Evidence that the predisposing locus is not on the long arm of chromosome 7.
    Shannon KM; Turhan AG; Chang SS; Bowcock AM; Rogers PC; Carroll WL; Cowan MJ; Glader BE; Eaves CJ; Eaves AC
    J Clin Invest; 1989 Sep; 84(3):984-9. PubMed ID: 2569483
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases.
    Le Beau MM; Espinosa R; Davis EM; Eisenbart JD; Larson RA; Green ED
    Blood; 1996 Sep; 88(6):1930-5. PubMed ID: 8822909
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Delineation of multiple deleted regions in 7q in myeloid disorders.
    Tosi S; Scherer SW; Giudici G; Czepulkowski B; Biondi A; Kearney L
    Genes Chromosomes Cancer; 1999 Aug; 25(4):384-92. PubMed ID: 10398433
    [TBL] [Abstract][Full Text] [Related]  

  • 10. c-src is consistently conserved in the chromosomal deletion (20q) observed in myeloid disorders.
    Le Beau MM; Westbrook CA; Diaz MO; Rowley JD
    Proc Natl Acad Sci U S A; 1985 Oct; 82(19):6692-6. PubMed ID: 2413444
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7.
    Shannon KM; Turhan AG; Rogers PC; Kan YW
    Genomics; 1992 Sep; 14(1):121-5. PubMed ID: 1358790
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Assignment of CSF-1 to 5q33.1: evidence for clustering of genes regulating hematopoiesis and for their involvement in the deletion of the long arm of chromosome 5 in myeloid disorders.
    Pettenati MJ; Le Beau MM; Lemons RS; Shima EA; Kawasaki ES; Larson RA; Sherr CJ; Diaz MO; Rowley JD
    Proc Natl Acad Sci U S A; 1987 May; 84(9):2970-4. PubMed ID: 3495006
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome.
    Jotterand Bellomo M; Parlier V; Mühlematter D; Grob JP; Beris P
    Cancer Genet Cytogenet; 1992 Apr; 59(2):138-60. PubMed ID: 1581880
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22.
    Schwartz CE; Stanislovitis P; Phelan MC; Klinger K; Taylor HA; Stevenson RE
    Cytogenet Cell Genet; 1991; 56(3-4):152-3. PubMed ID: 2055109
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosome 20 deletions in myelodysplastic syndromes and Philadelphia-chromosome-negative myeloproliferative disorders: characterization by molecular cytogenetics of commonly deleted and retained regions.
    Douet-Guilbert N; Basinko A; Morel F; Le Bris MJ; Ugo V; Morice P; Berthou C; De Braekeleer M
    Ann Hematol; 2008 Jul; 87(7):537-44. PubMed ID: 18350294
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosome assignment and restriction fragment length polymorphism analysis of the anonymous DNA probe B79a at 7q22 (HMG8 assignment D7S13).
    Estivill X; Schmidtke J; Williamson R; Wainwright B
    Hum Genet; 1986 Nov; 74(3):320-2. PubMed ID: 2877942
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase.
    Fagan K; Gill A; Henry R; Wilkinson I; Carey B
    J Med Genet; 1989 Oct; 26(10):619-25. PubMed ID: 2486209
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Detection of chromosome 20q deletions in bone marrow metaphases but not peripheral blood granulocytes in patients with myeloproliferative disorders or myelodysplastic syndromes.
    Asimakopoulos FA; Holloway TL; Nacheva EP; Scott MA; Fenaux P; Green AR
    Blood; 1996 Feb; 87(4):1561-70. PubMed ID: 8608248
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2.
    Scheurlen WG; Seranski P; Mincheva A; Kühl J; Sörensen N; Krauss J; Lichter P; Poustka A; Wilgenbus KK
    Genes Chromosomes Cancer; 1997 Jan; 18(1):50-8. PubMed ID: 8993980
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosome 7 monosomy and deletions in myeloproliferative diseases.
    Tripputi P; Cassani B; Alfano R; Graziani D; Cigognini D; Doi P; Bignotto M; Corneo G; Coggi G
    Leuk Res; 2001 Sep; 25(9):735-9. PubMed ID: 11489466
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.