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 *

85 related articles for article (PubMed ID: 6497930)

  • 1. The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemia.
    Humphries SE; Donald JA; McFadden JJ; Shull S; Williamson R; Jowett NI; Galton DJ; Julsrud JO; Berg K; Heiberg A
    Atherosclerosis; 1984 Sep; 52(3):267-78. PubMed ID: 6497930
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage relationships of the gene for apolipoprotein CII with loci on chromosome 19.
    Donald JA; Wallis SC; Kessling A; Tippett P; Robson EB; Ball S; Davies KE; Scambler P; Berg K; Heiberg A
    Hum Genet; 1985; 69(1):39-43. PubMed ID: 3855405
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The locus for apolipoprotein E (apoE) is linked to the complement component C3 (C3) locus on chromosome 19 in man.
    Olaisen B; Teisberg P; Gedde-Dahl T
    Hum Genet; 1982; 62(3):233-6. PubMed ID: 7169215
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The locus for apolipoprotein E (apoE) is close to the Lutheran (Lu) blood group locus on chromosome 19.
    Gedde-Dahl T; Olaisen B; Teisberg P; Wilhelmy MC; Mevåg B; Helland R
    Hum Genet; 1984; 67(2):178-82. PubMed ID: 6745937
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Approximate linkage equilibrium between two polymorphic sites within the gene for human complement component 3.
    Donald JA; Ball SP
    Ann Hum Genet; 1984 Jul; 48(3):269-73. PubMed ID: 6465843
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutation in the ARH gene and a chromosome 13q locus influence cholesterol levels in a new form of digenic-recessive familial hypercholesterolemia.
    Al-Kateb H; Bähring S; Hoffmann K; Strauch K; Busjahn A; Nürnberg G; Jouma M; Bautz EK; Dresel HA; Luft FC
    Circ Res; 2002 May; 90(9):951-8. PubMed ID: 12016260
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Haplotype associations of three DNA polymorphisms at the human low density lipoprotein receptor gene locus in familial hypercholesterolaemia.
    Kotze MJ; Langenhoven E; Retief AE; Steyn K; Marais MP; Grobbelaar JJ; Oosthuizen CJ; Weich HF; Benadé AJ
    J Med Genet; 1987 Dec; 24(12):750-5. PubMed ID: 3430554
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage study of the low-density lipoprotein-receptor gene and cholesterol levels in an Afrikaner family. Quantitative genetics and identification of a minor founder effect.
    Brink PA; Brink LT; Torrington M; Bester AJ
    S Afr Med J; 1990 Mar; 77(6):292-6. PubMed ID: 1969180
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Linkage of the LW blood group locus with the complement C3 and Lutheran blood group loci.
    Sistonen P
    Ann Hum Genet; 1984 Jul; 48(3):239-42. PubMed ID: 6431896
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spectrum of LDLR gene mutations, including a novel mutation causing familial hypercholesterolaemia, in North-western Greece.
    Diakou M; Miltiadous G; Xenophontos SL; Manoli P; Cariolou MA; Elisaf M
    Eur J Intern Med; 2011 Oct; 22(5):e55-9. PubMed ID: 21925044
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical experience of scoring criteria for Familial Hypercholesterolaemia (FH) genetic testing in Wales.
    Haralambos K; Whatley SD; Edwards R; Gingell R; Townsend D; Ashfield-Watt P; Lansberg P; Datta DB; McDowell IF
    Atherosclerosis; 2015 May; 240(1):190-6. PubMed ID: 25797312
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis.
    Humphries SE; Kessling AM; Horsthemke B; Donald JA; Seed M; Jowett N; Holm M; Galton DJ; Wynn V; Williamson R
    Lancet; 1985 May; 1(8436):1003-5. PubMed ID: 2859461
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.
    Davies KE; Jackson J; Williamson R; Harper PS; Ball S; Sarfarazi M; Meredith L; Fey G
    J Med Genet; 1983 Aug; 20(4):259-63. PubMed ID: 6620325
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Six DNA polymorphisms in the low density lipoprotein receptor gene: their genetic relationship and an example of their use for identifying affected relatives of patients with familial hypercholesterolaemia.
    Humphries S; King-Underwood L; Gudnason V; Seed M; Delattre S; Clavey V; Fruchart JC
    J Med Genet; 1993 Apr; 30(4):273-9. PubMed ID: 8098067
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindreds.
    Haddad L; Day LB; Attwood J; Povey S; Humphries SE; Day IN
    Ann Hum Genet; 1997 Nov; 61(Pt 6):497-506. PubMed ID: 9543550
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Use of DNA haplotype analysis in diagnosis of familial hypercholesterolaemia in 31 German families.
    Schuster H; Rauh G; Gerl C; Keller C; Wolfram G; Zöllner N
    J Med Genet; 1991 Dec; 28(12):865-70. PubMed ID: 1684620
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fine mapping of low-density lipoprotein receptor gene by genetic linkage on chromosome 19p13.1-p13.3 and study of the founder effect of four French Canadian low-density lipoprotein receptor gene mutations.
    Couture P; Morissette J; Gaudet D; Vohl MC; Gagné C; Bergeron J; Després JP; Simard J
    Atherosclerosis; 1999 Mar; 143(1):145-51. PubMed ID: 10208489
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK
    Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A study of familial hypercholesterolaemia in Iceland using RFLPs.
    Taylor R; Bryant J; Gudnason V; Sigurdsson G; Humphries S
    J Med Genet; 1989 Aug; 26(8):494-8. PubMed ID: 2570157
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19.
    Eiberg H; Mohr J; Nielsen LS; Simonsen N
    Clin Genet; 1983 Sep; 24(3):159-70. PubMed ID: 6627719
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.