BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 11311134)

  • 1. Cloning, expression and localization of human BM88 shows that it maps to chromosome 11p15.5, a region implicated in Beckwith-Wiedemann syndrome and tumorigenesis.
    Gaitanou M; Buanne P; Pappa C; Georgopoulou N; Mamalaki A; Tirone F; Matsas R
    Biochem J; 2001 May; 355(Pt 3):715-24. PubMed ID: 11311134
    [TBL] [Abstract][Full Text] [Related]  

  • 2. C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5.
    Zhu X; Higashimoto K; Soejima H; Yatsuki H; Sugihara H; Mukai T; Joh K
    Gene; 2000 Oct; 256(1-2):311-7. PubMed ID: 11054561
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain.
    Cooper PR; Smilinich NJ; Day CD; Nowak NJ; Reid LH; Pearsall RS; Reece M; Prawitt D; Landers J; Housman DE; Winterpacht A; Zabel BU; Pelletier J; Weissman BE; Shows TB; Higgins MJ
    Genomics; 1998 Apr; 49(1):38-51. PubMed ID: 9570947
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Expression pattern of BM88 in the developing nervous system of the chick and mouse embryo.
    Politis PK; Rohrer H; Matsas R
    Gene Expr Patterns; 2007 Jan; 7(1-2):165-77. PubMed ID: 16949349
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Human FRAG1 encodes a novel membrane-spanning protein that localizes to chromosome 11p15.5, a region of frequent loss of heterozygosity in cancer.
    Lorenzi MV; Castagnino P; Aaronson DC; Lieb DC; Lee CC; Keck CL; Popescu NC; Miki T
    Genomics; 1999 Nov; 62(1):59-66. PubMed ID: 10585768
    [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. 11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.
    Puech A; Ahnine L; Lüdecke HJ; Senger G; Ivens A; Jeanpierre C; Little P; Horsthemke B; Claussen U; Jones C
    Genomics; 1992 Aug; 13(4):1274-80. PubMed ID: 1380484
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The BM88 antigen, a novel neuron-specific molecule, enhances the differentiation of mouse neuroblastoma cells.
    Mamalaki A; Boutou E; Hurel C; Patsavoudi E; Tzartos S; Matsas R
    J Biol Chem; 1995 Jun; 270(23):14201-8. PubMed ID: 7775480
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular cloning and in situ localization of the human contactin gene (CNTN1) on chromosome 12q11-q12.
    Berglund EO; Ranscht B
    Genomics; 1994 Jun; 21(3):571-82. PubMed ID: 7959734
    [TBL] [Abstract][Full Text] [Related]  

  • 10. BM88 is an early marker of proliferating precursor cells that will differentiate into the neuronal lineage.
    Koutmani Y; Hurel C; Patsavoudi E; Hack M; Gotz M; Thomaidou D; Matsas R
    Eur J Neurosci; 2004 Nov; 20(10):2509-23. PubMed ID: 15548196
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression.
    Prawitt D; Enklaar T; Klemm G; Gärtner B; Spangenberg C; Winterpacht A; Higgins M; Pelletier J; Zabel B
    Hum Mol Genet; 2000 Jan; 9(2):203-16. PubMed ID: 10607831
    [TBL] [Abstract][Full Text] [Related]  

  • 12. JH8, a gene highly homologous to the mouse jerky gene, maps to the region for childhood absence epilepsy on 8q24.
    Morita R; Miyazaki E; Fong CY; Chen XN; Korenberg JR; Delgado-Escueta AV; Yamakawa K
    Biochem Biophys Res Commun; 1998 Jul; 248(2):307-14. PubMed ID: 9675132
    [TBL] [Abstract][Full Text] [Related]  

  • 13. cDNA cloning and chromosome mapping of the human Fe65 gene: interaction of the conserved cytoplasmic domains of the human beta-amyloid precursor protein and its homologues with the mouse Fe65 protein.
    Bressler SL; Gray MD; Sopher BL; Hu Q; Hearn MG; Pham DG; Dinulos MB; Fukuchi K; Sisodia SS; Miller MA; Disteche CM; Martin GM
    Hum Mol Genet; 1996 Oct; 5(10):1589-98. PubMed ID: 8894693
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.
    Redeker E; Alders M; Hoovers JM; Richard CW; Westerveld A; Mannens M
    Cytogenet Cell Genet; 1995; 68(3-4):222-5. PubMed ID: 7842740
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The human MyoD1 (MYF3) gene maps on the short arm of chromosome 11 but is not associated with the WAGR locus or the region for the Beckwith-Wiedemann syndrome.
    Gessler M; Hameister H; Henry I; Junien C; Braun T; Arnold HH
    Hum Genet; 1990 Dec; 86(2):135-8. PubMed ID: 2176177
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type.
    Crider-Miller SJ; Reid LH; Higgins MJ; Nowak NJ; Shows TB; Futreal PA; Weissman BE
    Genomics; 1997 Dec; 46(3):355-63. PubMed ID: 9441738
    [TBL] [Abstract][Full Text] [Related]  

  • 17. cDNA cloning, molecular characterization, and chromosomal localization of NET(EPHT2), a human EPH-related receptor protein-tyrosine kinase gene preferentially expressed in brain.
    Tang XX; Biegel JA; Nycum LM; Yoshioka A; Brodeur GM; Pleasure DE; Ikegaki N
    Genomics; 1995 Sep; 29(2):426-37. PubMed ID: 8666391
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification and chromosome mapping of the mouse homologue of the human gene (DDX6) that encodes a putative RNA helicase of the DEAD box protein family.
    Akao Y; Matsuda Y
    Cytogenet Cell Genet; 1996; 75(1):38-44. PubMed ID: 8995487
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.
    Cooper PR; Nowak NJ; Higgins MJ; Church DM; Shows TB
    Genomics; 1998 May; 49(3):419-29. PubMed ID: 9615227
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isolation of cDNAs from the Cri-du-chat critical region by direct screening of a chromosome 5-specific cDNA library.
    Simmons AD; Overhauser J; Lovett M
    Genome Res; 1997 Feb; 7(2):118-27. PubMed ID: 9049630
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.