BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

392 related articles for article (PubMed ID: 8104627)

  • 1. The isolation of a yeast artificial chromosome (YAC) contig extending for 2 megabases in the vicinity of the von Hippel Lindau disease gene.
    Liu W; Piechocki M; Shridhar V; Lyles G; Song Z; Nakamura Y; Drabkin H; Vance J; Smith DI
    Hum Mol Genet; 1993 Aug; 2(8):1177-82. PubMed ID: 8104627
    [TBL] [Abstract][Full Text] [Related]  

  • 2. One-megabase yeast artificial chromosome and 400-kilobase cosmid-phage contigs containing the von Hippel-Lindau tumor suppressor and Ca(2+)-transporting adenosine triphosphatase isoform 2 genes.
    Kuzmin I; Stackhouse T; Latif F; Duh FM; Geil L; Gnarra J; Yao M; Orcutt ML; Li H; Tory K
    Cancer Res; 1994 May; 54(9):2486-91. PubMed ID: 8162598
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell lines.
    Francis F; Benham F; See CG; Fox M; Ishikawa-Brush Y; Monaco AP; Weiss B; Rappold G; Hamvas RM; Lehrach H
    Genomics; 1994 Mar; 20(1):75-83. PubMed ID: 8020959
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Construction of a YAC contig and a STS map spanning at least seven megabasepairs in chromosome 5q34-35.
    Lu-Kuo JM; Le Paslier D; Weissenbach J; Chumakov I; Cohen D; Ward DC
    Hum Mol Genet; 1994 Jan; 3(1):99-106. PubMed ID: 8162060
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A cosmid and yeast artificial chromosome contig containing the complete ryanodine receptor (RYR1) gene.
    Rouquier S; Giorgi D; Trask B; Bergmann A; Phillips MS; MacLennan DH; de Jong P
    Genomics; 1993 Aug; 17(2):330-40. PubMed ID: 8406483
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Yeast artificial chromosome cloning of 3.2 megabases within chromosomal band 11q24 closely linking c-ets 1 and Fli-1 and encompassing the Ewing sarcoma breakpoint.
    Selleri L; Giovannini M; Hermanson GG; Romo A; Quackenbush J; Penny L; Khristich JV; Evans GA
    Genomics; 1994 Jul; 22(1):137-47. PubMed ID: 7959760
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An integrated YAC-overlap and 'cosmid-pocket' map of the human chromosome 21.
    Nizetić D; Gellen L; Hamvas RM; Mott R; Grigoriev A; Vatcheva R; Zehetner G; Yaspo ML; Dutriaux A; Lopes C
    Hum Mol Genet; 1994 May; 3(5):759-70. PubMed ID: 8081363
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26.
    Pericak-Vance MA; Nunes KJ; Whisenant E; Loeb DB; Small KW; Stajich JM; Rimmler JB; Yamaoka LH; Smith DI; Drabkin HA
    J Med Genet; 1993 Jun; 30(6):487-91. PubMed ID: 8100855
    [TBL] [Abstract][Full Text] [Related]  

  • 9. High-resolution physical mapping of a 6.7-Mb YAC contig spanning a region critical for the monosomy 21 phenotype in 21q21.3-q22.1.
    Orti R; Mégarbane A; Maunoury C; Van Broeckhoven C; Sinet PM; Delabar JM
    Genomics; 1997 Jul; 43(1):25-33. PubMed ID: 9226369
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb.
    Banfi S; Chung MY; Kwiatkowski TJ; Ranum LP; McCall AE; Chinault AC; Orr HT; Zoghbi HY
    Genomics; 1993 Dec; 18(3):627-35. PubMed ID: 8307572
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Construction of 110 cosmid markers and a 4.5-Mb YAC contig on human chromosome 8p12-q11.
    Kurimasa A; Suzuki N; Kumano S; Li H; Wells D; Wagner MJ; Chen F; Chen DJ; Oshimura M
    Genomics; 1995 Jul; 28(2):147-53. PubMed ID: 8530020
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A 6-Mb yeast artificial chromosome contig and long-range physical map encompassing the region on chromosome 12q15 frequently rearranged in a variety of benign solid tumors.
    Schoenmakers EF; Geurts JM; Kools PF; Mols R; Huysmans C; Bullerdiek J; Van den Berghe H; Van de Ven WJ
    Genomics; 1995 Oct; 29(3):665-78. PubMed ID: 8575759
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3.
    Sood R; Blake T; Aksentijevich I; Wood G; Chen X; Gardner D; Shelton DA; Mangelsdorf M; Orsborn A; Pras E; Balow JE; Centola M; Deng Z; Zaks N; Chen X; Richards N; Fischel-Ghodsian N; Rotter JI; Pras M; Shohat M; Deaven LL; Gumucio DL; Callen DF; Richards RI; Doggett NA
    Genomics; 1997 May; 42(1):83-95. PubMed ID: 9177779
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease.
    Seizinger BR; Smith DI; Filling-Katz MR; Neumann H; Green JS; Choyke PL; Anderson KM; Freiman RN; Klauck SM; Whaley J
    Proc Natl Acad Sci U S A; 1991 Apr; 88(7):2864-8. PubMed ID: 2011596
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of a YAC and cosmid contig containing markers tightly linked to the myotonic dystrophy locus on chromosome 19.
    Buxton J; Shelbourne P; Davies J; Jones C; Perryman MB; Ashizawa T; Butler R; Brook D; Shaw D; de Jong P
    Genomics; 1992 Jul; 13(3):526-31. PubMed ID: 1639381
    [TBL] [Abstract][Full Text] [Related]  

  • 16. cA479 (D3S719): a cosmid mapped telomeric of the Von Hippel Lindau disease gene contains the D3S18 locus.
    Liu W; Vance J; Smith DI
    Hum Mol Genet; 1992 Jun; 1(3):201. PubMed ID: 1303179
    [No Abstract]   [Full Text] [Related]  

  • 17. Molecular characterization of a novel human gene, SEC13R, related to the yeast secretory pathway gene SEC13, and mapping to a conserved linkage group on human chromosome 3p24-p25 and mouse chromosome 6.
    Swaroop A; Yang-Feng TL; Liu W; Gieser L; Barrow LL; Chen KC; Agarwal N; Meisler MH; Smith DI
    Hum Mol Genet; 1994 Aug; 3(8):1281-6. PubMed ID: 7987303
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locus.
    Crossey PA; Maher ER; Jones MH; Richards FM; Latif F; Phipps ME; Lush M; Foster K; Tory K; Green JS
    Hum Mol Genet; 1993 Mar; 2(3):279-82. PubMed ID: 8499917
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene.
    Richards FM; Maher ER; Latif F; Phipps ME; Tory K; Lush M; Crossey PA; Oostra B; Enblad P; Gustavson KH
    J Med Genet; 1993 Feb; 30(2):104-7. PubMed ID: 8445612
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
    Yu CE; Oshima J; Hisama FM; Matthews S; Trask BJ; Schellenberg GD
    Genomics; 1996 Aug; 35(3):431-40. PubMed ID: 8812476
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.