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 *

181 related articles for article (PubMed ID: 1971150)

  • 1. 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]  

  • 2. Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q.
    Cavanna JS; Greenfield AJ; Johnson KJ; Marks AR; Nadal-Ginard B; Brown SD
    Genomics; 1990 May; 7(1):12-8. PubMed ID: 1970795
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy.
    Johnson KJ; Jones PJ; Spurr N; Nimmo E; Davies J; Creed H; Weiss M; Williamson R
    Cytogenet Cell Genet; 1988; 48(1):13-5. PubMed ID: 2460293
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ryanodine receptor gene is a candidate for predisposition to malignant hyperthermia.
    MacLennan DH; Duff C; Zorzato F; Fujii J; Phillips M; Korneluk RG; Frodis W; Britt BA; Worton RG
    Nature; 1990 Feb; 343(6258):559-61. PubMed ID: 1967823
    [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. Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.
    Harley HG; Walsh KV; Rundle S; Brook JD; Sarfarazi M; Koch MC; Floyd JL; Harper PS; Shaw DJ
    Hum Genet; 1991 May; 87(1):73-80. PubMed ID: 2037285
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. High-resolution physical mapping of four microsatellite repeat markers near the RYR1 locus on chromosome 19q13.1 and apparent exclusion of the MHS locus from this region in two malignant hyperthermia susceptible families.
    Iles DE; Segers B; Heytens L; Sengers RC; Wieringa B
    Genomics; 1992 Nov; 14(3):749-54. PubMed ID: 1427902
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus.
    Korneluk RG; MacKenzie AE; Nakamura Y; Dubé I; Jacob P; Hunter AG
    Genomics; 1989 Oct; 5(3):596-604. PubMed ID: 2613241
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus.
    Shaw DJ; Meredith AL; Sarfarazi M; Huson SM; Brook JD; Myklebost O; Harper PS
    Hum Genet; 1985; 70(3):271-3. PubMed ID: 2991117
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.
    Walsh KV; Harley HG; Brook JD; Rundle SA; Sarfarazi M; Harper PS; Shaw DJ
    Hum Genet; 1990 Aug; 85(3):305-10. PubMed ID: 1975560
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19.
    Kausch K; Lehmann-Horn F; Janka M; Wieringa B; Grimm T; Müller CR
    Genomics; 1991 Jul; 10(3):765-9. PubMed ID: 1889818
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cloning of the essential myotonic dystrophy region and mapping of the putative defect.
    Aslanidis C; Jansen G; Amemiya C; Shutler G; Mahadevan M; Tsilfidis C; Chen C; Alleman J; Wormskamp NG; Vooijs M
    Nature; 1992 Feb; 355(6360):548-51. PubMed ID: 1346925
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.
    Shutler G; Korneluk RG; Tsilfidis C; Mahadevan M; Bailly J; Smeets H; Jansen G; Wieringa B; Lohman F; Aslanidis C
    Genomics; 1992 Jul; 13(3):518-25. PubMed ID: 1639380
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19.
    Shaw DJ; Meredith AL; Brook JD; Sarfarzi M; Harley HG; Huson SM; Bell GI; Harper PS
    Hum Genet; 1986 Nov; 74(3):267-9. PubMed ID: 2877934
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Recombination events that locate myotonic dystrophy distal to APOC2 on 19q.
    Johnson K; Shelbourne P; Davies J; Buxton J; Nimmo E; Anvret M; Bonduelle M; Williamson B; Savontaus ML
    Genomics; 1989 Nov; 5(4):746-51. PubMed ID: 2591962
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The syntenic relationship of proximal mouse chromosome 7 and the myotonic dystrophy gene region on human chromosome 19q.
    Saunders AM; Seldin MF
    Genomics; 1990 Feb; 6(2):324-32. PubMed ID: 2307474
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.