BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

119 related articles for article (PubMed ID: 1385297)

  • 1. Genetic and physical map of the interferon region on chromosome 9p.
    Fountain JW; Karayiorgou M; Taruscio D; Graw SL; Buckler AJ; Ward DC; Dracopoli NC; Housman DE
    Genomics; 1992 Sep; 14(1):105-12. PubMed ID: 1385297
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Homozygous deletions within human chromosome band 9p21 in melanoma.
    Fountain JW; Karayiorgou M; Ernstoff MS; Kirkwood JM; Vlock DR; Titus-Ernstoff L; Bouchard B; Vijayasaradhi S; Houghton AN; Lahti J
    Proc Natl Acad Sci U S A; 1992 Nov; 89(21):10557-61. PubMed ID: 1438246
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular deletion of 9p sequences in non-small cell lung cancer and malignant mesothelioma.
    Center R; Lukeis R; Dietzsch E; Gillespie M; Garson OM
    Genes Chromosomes Cancer; 1993 May; 7(1):47-53. PubMed ID: 7688555
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular definition of a chromosome 9p21 germ-line deletion in a woman with multiple melanomas and a plexiform neurofibroma: implications for 9p tumor-suppressor gene(s).
    Petty EM; Gibson LH; Fountain JW; Bolognia JL; Yang-Feng TL; Housman DE; Bale AE
    Am J Hum Genet; 1993 Jul; 53(1):96-104. PubMed ID: 8317504
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homozygous deletions within 9p21-p22 identify a small critical region of chromosomal loss in human malignant mesotheliomas.
    Cheng JQ; Jhanwar SC; Lu YY; Testa JR
    Cancer Res; 1993 Oct; 53(20):4761-3. PubMed ID: 8402655
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia.
    Olopade OI; Bohlander SK; Pomykala H; Maltepe E; Van Melle E; Le Beau MM; Diaz MO
    Genomics; 1992 Oct; 14(2):437-43. PubMed ID: 1385305
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.
    Hanauer A; Chery M; Fujita R; Driesel AJ; Gilgenkrantz S; Mandel JL
    Am J Hum Genet; 1990 Jan; 46(1):133-7. PubMed ID: 2294745
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The CEPH consortium linkage map of human chromosome 1.
    Dracopoli NC; O'Connell P; Elsner TI; Lalouel JM; White RL; Buetow KH; Nishimura DY; Murray JC; Helms C; Mishra SK
    Genomics; 1991 Apr; 9(4):686-700. PubMed ID: 2037294
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A genetic linkage map of 96 loci on the short arm of human chromosome 3.
    Tory K; Latif F; Modi W; Schmidt L; Wei MH; Li H; Cobler P; Orcutt ML; Delisio J; Geil L
    Genomics; 1992 Jun; 13(2):275-86. PubMed ID: 1612588
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Construction of a GT polymorphism map of human 9q.
    Kwiatkowski DJ; Henske EP; Weimer K; Ozelius L; Gusella JF; Haines J
    Genomics; 1992 Feb; 12(2):229-40. PubMed ID: 1339384
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome.
    Arveiler B; Oberlé I; Mandel JL
    Genomics; 1987 Sep; 1(1):60-6. PubMed ID: 2889662
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CEPH consortium Map of chromosome 9.
    Attwood J; Chiano M; Collins A; Donis-Keller H; Dracopoli N; Fountain J; Falk C; Goudie D; Gusella J; Haines J
    Genomics; 1994 Jan; 19(2):203-14. PubMed ID: 8188250
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Centre d'Etude de Polymorphisme Humain.
    Westbrook CA; Le Beau MM; Neuman WL; Keinanen M; Yamaoka LH; Speer MC; Espinosa R; Nakamura Y; Williamson R; Mullan M
    Cytogenet Cell Genet; 1994; 67(2):86-93. PubMed ID: 7913678
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The CEPH consortium linkage map of human chromosome 2.
    Spurr NK; Cox S; Bryant SP; Attwood J; Robson EB; Shields DC; Steinbrueck T; Jenkins T; Murray JC; Kidd KK
    Genomics; 1992 Dec; 14(4):1055-63. PubMed ID: 1478647
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diffuse large cell lymphomas exhibit frequent deletions in 9p21-22 and 9q31-34 regions.
    Chaganti SR; Gaidano G; Louie DC; Dalla-Favera R; Chaganti RS
    Genes Chromosomes Cancer; 1995 Jan; 12(1):32-6. PubMed ID: 7534108
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A genetic linkage map of 32 loci on human chromosome 10.
    Bowden DW; Gravius TC; Green P; Falls K; Wurster-Hill D; Noll W; Müller-Kahle H; Donis-Keller H
    Genomics; 1989 Nov; 5(4):718-26. PubMed ID: 2574142
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heterogeneity, polyploidy, aneusomy, and 9p deletion in human glioblastoma multiforme.
    Park SH; Maeda T; Mohapatra G; Waldman FM; Davis RL; Feuerstein BG
    Cancer Genet Cytogenet; 1995 Sep; 83(2):127-35. PubMed ID: 7553582
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Integrated genetic map of human chromosome 2.
    Cox S; Bryant SP; Collins A; Weissenbach J; Donis-Keller H; Koeleman BP; Steinkasserer A; Spurr NK
    Ann Hum Genet; 1995 Oct; 59(4):413-34. PubMed ID: 8579334
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of a novel region of homozygous deletion on chromosome 9p in squamous cell carcinoma of the lung: the location of a putative tumor suppressor gene.
    Wiest JS; Franklin WA; Otstot JT; Forbey K; Varella-Garcia M; Rao K; Drabkin H; Gemmill R; Ahrent S; Sidransky D; Saccomanno G; Fountain JW; Anderson MW
    Cancer Res; 1997 Jan; 57(1):1-6. PubMed ID: 8988029
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic mapping of the erythropoietin receptor gene.
    Sistonen P; Träskelin AL; Lehväslaiho H; de la Chapelle A
    Hum Genet; 1993 Oct; 92(3):299-301. PubMed ID: 8406437
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.