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 *

84 related articles for article (PubMed ID: 1001030)

  • 1. Human breast carcinomas: marker chromosomes involving 1q in seven cases.
    Cruciger QV; Pathak S; Cailleau R
    Cytogenet Cell Genet; 1976; 17(4):231-5. PubMed ID: 1001030
    [No Abstract]   [Full Text] [Related]  

  • 2. Cytogenetic analysis on eight human breast tumor cell lines: high frequencies of 1q, 11q and HeLa-like marker chromosomes.
    Satya-Prakash KL; Pathak S; Hsu TC; Olivé M; Cailleau R
    Cancer Genet Cytogenet; 1981 Jan; 3(1):61-73. PubMed ID: 7272986
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Preferential involvement of chromosome 1q in a primary breast carcinoma.
    Kovacs G
    Cancer Genet Cytogenet; 1981 Mar; 3(2):125-9. PubMed ID: 7272991
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Abnormalities of chromosome No. 1 in human solid malignant tumours.
    Kovacs G
    Int J Cancer; 1978 Jun; 21(6):688-94. PubMed ID: 669851
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cytogenetic analysis of metastatic effusions from breast tumors.
    Bello MJ; Rey JA
    Neoplasma; 1989; 36(1):71-81. PubMed ID: 2704425
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pseudodiploid karyotype in a breast carcinoma.
    Bodor F; Håkansson CH; Norgren A
    Acta Pathol Microbiol Scand A; 1974 May; 82(3):386-8. PubMed ID: 4853934
    [No Abstract]   [Full Text] [Related]  

  • 7. A human breast adenocarcinoma with chromosome and isoenzyme markers similar to those of the HeLa line.
    Pathak S; Siciliano MJ; Cailleau R; Wiseman CL; Hsu TC
    J Natl Cancer Inst; 1979 Feb; 62(2):263-71. PubMed ID: 283262
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Chromosome anomalies in 2 cases of human ovarian cancer].
    de Blois MC; Boyer P; Bénard J; Riou G
    C R Acad Sci III; 1986; 302(3):81-6. PubMed ID: 3082479
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [A Dutch chromosome abnormality in myelodysplasia?].
    Scheres JM; Hustinx TW; Geraedts JP; Leeksma CH; Holdrinet RS
    Ned Tijdschr Geneeskd; 1985 Sep; 129(37):1783-7. PubMed ID: 4069238
    [No Abstract]   [Full Text] [Related]  

  • 10. Observations on nuclear protrusions and the length of long arms of abnormal chromosomes in malignancy.
    Kovacs G
    Acta Cytol; 1982; 26(2):247-50. PubMed ID: 6952728
    [TBL] [Abstract][Full Text] [Related]  

  • 11. G-banding of 3 multiple myeloma marker chromosomes.
    Philip P; Drivsholm AA
    Biomedicine; 1974 Nov; 21(11):429-30. PubMed ID: 4142930
    [No Abstract]   [Full Text] [Related]  

  • 12. Masked Philadelphia chromosome due to the translocation (1q-;22q +) and small chromosome 19 in a case of acute leukemia.
    Suciu S; Marinca E; Gădăleanu V
    Neoplasma; 1984; 31(5):573-9. PubMed ID: 6594592
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosome abnormalities in tumor cells from patients with sporadic Wilms' tumor.
    Kondo K; Chilcote RR; Maurer HS; Rowley JD
    Cancer Res; 1984 Nov; 44(11):5376-81. PubMed ID: 6091875
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Are 1q plus chromosomes harmless?
    Gardner RJ; McCreanor HR; Parslow MI; Veale AM
    Clin Genet; 1974; 6(5):383-93. PubMed ID: 4434654
    [No Abstract]   [Full Text] [Related]  

  • 15. Chromosomes as markers in human cancer.
    Sandberg AA
    Int Adv Surg Oncol; 1981; 4():311-36. PubMed ID: 7019095
    [No Abstract]   [Full Text] [Related]  

  • 16. Translocation t(1;10) (q21;q26) in a case of acute nonlymphocytic leukemia.
    Terreros MC; Quesada M; Slavutsky IR
    Acta Haematol; 1998; 99(2):92-4. PubMed ID: 9554457
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Abnormalities of chromosome involving 1q in uterine endometrial carcinomas].
    Fujita H; Wake N; Sakai K; Hashimoto M; Okuyama K; Kutsuzawa T; Ichinoe K
    Nihon Sanka Fujinka Gakkai Zasshi; 1986 Feb; 38(2):236-42. PubMed ID: 3457090
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Observation of 7 cases of rare autosomal pathology. Trisomy 9p; monosomy 18q; ring 21; trisomy 6p; trisomy 2q 1-21 translocation].
    Fioretti G; Pagano L; Renda S; Festa B; Rinaldi A; Celona A; Casullo C; Stabile M; Cavaliere ML; Ventruto V
    Minerva Pediatr; 1980 Jun; 32(12):807-14. PubMed ID: 7464734
    [No Abstract]   [Full Text] [Related]  

  • 19. [46, XX, 1q-, 2q-, Dq+, 16q+ karyotype in a polymalformed child].
    de Grouchy J; Lautmann F
    Ann Genet; 1968 Jun; 11(2):129-31. PubMed ID: 5303425
    [No Abstract]   [Full Text] [Related]  

  • 20. Human neuroblastomas and abnormalities of chromosomes 1 and 17.
    Gilbert F; Feder M; Balaban G; Brangman D; Lurie DK; Podolsky R; Rinaldt V; Vinikoor N; Weisband J
    Cancer Res; 1984 Nov; 44(11):5444-9. PubMed ID: 6488196
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.