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 *

113 related articles for article (PubMed ID: 8188285)

  • 1. Molecular sublocalization and characterization of the 11;22 translocation breakpoint in a malignant rhabdoid tumor.
    Newsham I; Daub D; Besnard-Guerin C; Cavenee W
    Genomics; 1994 Feb; 19(3):433-40. PubMed ID: 8188285
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG
    Verh K Acad Geneeskd Belg; 1995; 57(5):389-422. PubMed ID: 8571670
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytogenetic and molecular analysis of a t(1;22)(p36;q11.2) in a rhabdoid tumor with a putative homozygous deletion of chromosome 22.
    Rosty C; Peter M; Zucman J; Validire P; Delattre O; Aurias A
    Genes Chromosomes Cancer; 1998 Feb; 21(2):82-9. PubMed ID: 9491318
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular definition in a somatic cell hybrid of a specific 2:13 translocation breakpoint in childhood rhabdomyosarcoma.
    Mitchell CD; Ventris JA; Warr TJ; Cowell JK
    Oncogene; 1991 Jan; 6(1):89-92. PubMed ID: 1992447
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
    Laureys G; Speleman F; Versteeg R; van der Drift P; Chan A; Leroy J; Francke U; Opdenakker G; Van Roy N
    Oncogene; 1995 Mar; 10(6):1087-93. PubMed ID: 7700633
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndrome.
    Negrini M; Sabbioni S; Ohta M; Veronese ML; Rattan S; Junien C; Croce CM
    Cancer Res; 1995 Jul; 55(13):2904-9. PubMed ID: 7796419
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [The neuroblastoma, "enfant terrible" among pediatric tumors].
    Laureys G
    Verh K Acad Geneeskd Belg; 2003; 65(1):5-23; discussion 23-8. PubMed ID: 12802894
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome.
    Ellison KA; Roth EJ; McCabe ER; Chinault AC; Zoghbi HY
    Am J Med Genet; 1993 Nov; 47(7):1124-34. PubMed ID: 8291533
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.
    Besnard-Guérin C; Newsham I; Winqvist R; Cavenee WK
    Hum Genet; 1996 Feb; 97(2):163-70. PubMed ID: 8566947
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular cytogenetic characterization of proximal-type epithelioid sarcoma.
    Lualdi E; Modena P; Debiec-Rychter M; Pedeutour F; Teixeira MR; Facchinetti F; Dagrada GP; Pilotti S; Sozzi G
    Genes Chromosomes Cancer; 2004 Nov; 41(3):283-90. PubMed ID: 15334553
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A 350-kb cosmid contig in 3p14.2 that crosses the t(3;8) hereditary renal cell carcinoma translocation breakpoint and 17 aphidicolin-induced FRA3B breakpoints.
    Paradee W; Wilke CM; Wang L; Shridhar R; Mullins CM; Hoge A; Glover TW; Smith DI
    Genomics; 1996 Jul; 35(1):87-93. PubMed ID: 8661108
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors.
    Newsham I; Kindler-Röhrborn A; Daub D; Cavenee W
    Genes Chromosomes Cancer; 1995 Jan; 12(1):1-7. PubMed ID: 7534105
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bipolar affective disorder partially cosegregates with a balanced t(9;11)(p24;q23.1) chromosomal translocation in a small pedigree.
    Baysal BE; Potkin SG; Farr JE; Higgins MJ; Korcz J; Gollin SM; James MR; Evans GA; Richard CW
    Am J Med Genet; 1998 Feb; 81(1):81-91. PubMed ID: 9514593
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Isolation of chromosome-specific DNA sequences from an Alu polymerase chain reaction library to define the breakpoint in a patient with a constitutional translocation t(1;13) (q22;q12) and ganglioneuroblastoma.
    Michalski AJ; Cotter FE; Cowell JK
    Oncogene; 1992 Aug; 7(8):1595-602. PubMed ID: 1630820
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Inactivation of the P16INK4/MTS1 gene by a chromosome translocation t(9;14)(p21-22;q11) in an acute lymphoblastic leukemia of B-cell type.
    Duro D; Bernard O; Della Valle V; Leblanc T; Berger R; Larsen CJ
    Cancer Res; 1996 Feb; 56(4):848-54. PubMed ID: 8631023
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The consistent 13q14 translocation breakpoint seen in chronic B-cell leukaemia (BCLL) involves deletion of the D13S25 locus which lies distal to the retinoblastoma predisposition gene.
    Hawthorn LA; Chapman R; Oscier D; Cowell JK
    Oncogene; 1993 Jun; 8(6):1415-9. PubMed ID: 8502470
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The t(11;22)(p15.5;q11.23) in a retroperitoneal rhabdoid tumor also includes a regional deletion distal to CRYBB2 on 22q.
    Besnard-Guérin C; Cavenee W; Newsham I
    Genes Chromosomes Cancer; 1995 Jul; 13(3):145-50. PubMed ID: 7669732
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosome 18 breakpoint in t(11;18)(q21;q21) translocation associated with MALT lymphoma is proximal to BCL2 and distal to DCC.
    Stoffel A; Rao PH; Louie DC; Krauter K; Liebowitz DN; Koeppen H; Le Beau MM; Chaganti RS
    Genes Chromosomes Cancer; 1999 Feb; 24(2):156-9. PubMed ID: 9885983
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chromosome 22q dosage in composite extrarenal rhabdoid tumors: clonal evolution or a phenotypic mimic?
    Fuller CE; Pfeifer J; Humphrey P; Bruch LA; Dehner LP; Perry A
    Hum Pathol; 2001 Oct; 32(10):1102-8. PubMed ID: 11679945
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Loss of heterozygosity at chromosome regions 22q11-12 and 11p15.5 in renal rhabdoid tumors.
    Schofield DE; Beckwith JB; Sklar J
    Genes Chromosomes Cancer; 1996 Jan; 15(1):10-7. PubMed ID: 8824720
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.