BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

6767 related articles for article (PubMed ID: 2564840)

  • 1. Confirmation and refinement of the localisation of the c-MEL locus on chromosome 19 by physical and genetic mapping.
    Nimmo E; Padua RA; Hughes D; Brook JD; Williamson R; Johnson KJ
    Hum Genet; 1989 Mar; 81(4):382-4. PubMed ID: 2564840
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosomal assignment of c-MEL, a human transforming oncogene, to chromosome 19 (p13.2-q13.2).
    Spurr NK; Hughes D; Goodfellow PN; Brook JD; Padua RA
    Somat Cell Mol Genet; 1986 Nov; 12(6):637-40. PubMed ID: 3466361
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Physical mapping of human chromosome 17 using fragment-containing microcell hybrids.
    Leach RJ; Thayer MJ; Schafer AJ; Fournier RE
    Genomics; 1989 Aug; 5(2):167-76. PubMed ID: 2571568
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A hypervariable region at the D19S11 locus.
    Buroker NE; Bufton L; Surti U; Leppert M; Kumlin E; Sheehy R; Magenis RE; Litt M
    Hum Genet; 1987 May; 76(1):90-5. PubMed ID: 2883111
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of radiation/fusion hybrids containing parts of human chromosome 10 and their use in mapping chromosome 10-specific probes.
    Rothschild CB; Noll WW; Gravius TC; Schuster MK; Nutile-McMenemy N; Jones C; Bowden DW
    Genomics; 1992 May; 13(1):25-34. PubMed ID: 1349579
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.
    Johnson K; Shelbourne P; Davies J; Buxton J; Nimmo E; Siciliano MJ; Bachinski LL; Anvret M; Harley H; Rundle S
    Am J Hum Genet; 1990 Jun; 46(6):1073-81. PubMed ID: 1971149
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy.
    Shutler G; MacKenzie AE; Brunner H; Wieringa B; de Jong P; Lohman FP; Leblond S; Bailly J; Korneluk RG
    Genomics; 1991 Mar; 9(3):500-4. PubMed ID: 1674498
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP.
    Geitvik GA; Høyheim B; Gedde-Dahl T; Grzeschik KH; Lothe R; Tomter H; Olaisen B
    Hum Genet; 1987 Nov; 77(3):205-9. PubMed ID: 2890568
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophy.
    Korneluk RG; MacLeod HL; McKeithan TW; Brooks JD; MacKenzie AE
    Genomics; 1989 Feb; 4(2):146-51. PubMed ID: 2567698
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.
    MacKenzie AE; Korneluk RG; Zorzato F; Fujii J; Phillips M; Iles D; Wieringa B; Leblond S; Bailly J; Willard HF
    Am J Hum Genet; 1990 Jun; 46(6):1082-9. PubMed ID: 1971150
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The beta subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies.
    Wu JS; Giuffra LA; Goodfellow PJ; Myers S; Carson NL; Anderson L; Hoyle LS; Simpson NE; Kidd KK
    Hum Genet; 1989 Nov; 83(4):383-90. PubMed ID: 2572537
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Regional localization of polymorphic markers on chromosome 10 by physical and genetic mapping.
    Mathew CG; Wakeling W; Jones E; Easton D; Fisher R; Strong C; Smith B; Chin K; Little P; Nakamura Y
    Ann Hum Genet; 1990 May; 54(2):121-9. PubMed ID: 1974407
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.
    Brunner HG; Smeets H; Lambermon HM; Coerwinkel-Driessen M; van Oost BA; Wieringa B; Ropers HH
    Genomics; 1989 Oct; 5(3):589-95. PubMed ID: 2575588
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Assignment of the erythropoietin receptor (EPOR) gene to mouse chromosome 9 and human chromosome 19.
    Budarf M; Huebner K; Emanuel B; Croce CM; Copeland NG; Jenkins NA; D'Andrea AD
    Genomics; 1990 Nov; 8(3):575-8. PubMed ID: 1962754
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus.
    Harley HG; Brook JD; Jackson CL; Glaser T; Walsh KV; Sarfarazi M; Kent R; Lager M; Koch M; Harper PS
    Genomics; 1988 Nov; 3(4):380-4. PubMed ID: 2907504
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genes.
    Lerman MI; Latif F; Glenn GM; Daniel LN; Brauch H; Hosoe S; Hampsch K; Delisio J; Orcutt ML; McBride OW
    Hum Genet; 1991 Apr; 86(6):567-77. PubMed ID: 1673958
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.
    Shaw DJ; Meredith AL; Sarfarazi M; Harley HG; Huson SM; Brook JD; Bufton L; Litt M; Mohandas T; Harper PS
    Hum Genet; 1986 Nov; 74(3):262-6. PubMed ID: 2877933
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Chromosomal assignment of the genes for proprotein convertases PC4, PC5, and PACE 4 in mouse and human.
    Mbikay M; Seidah NG; Chrétien M; Simpson EM
    Genomics; 1995 Mar; 26(1):123-9. PubMed ID: 7782070
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Physical mapping around the Alzheimer disease locus on the proximal long arm of chromosome 21.
    Owen MJ; James LA; Hardy JA; Williamson R; Goate AM
    Am J Hum Genet; 1990 Feb; 46(2):316-22. PubMed ID: 2301399
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids.
    Van Camp G; Van Hul W; Backhovens H; Stinissen P; Wehnert A; Patterson D; Vandenberghe A; Van Broeckhoven C
    Somat Cell Mol Genet; 1990 May; 16(3):241-9. PubMed ID: 1972817
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 339.