BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 8891387)

  • 1. A three-allelic polymorphic system in exon 12 of the LDL receptor gene is highly informative for segregation analysis of familial hypercholesterolemia in the Spanish population.
    Puig O; Chaves FJ; García-Sogo M; Real J; Gil JV; Armengod ME
    Clin Genet; 1996 Jul; 50(1):50-3. PubMed ID: 8891387
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Seven DNA polymorphisms in the LDL receptor gene: application to the study of familial hypercholesterolemia in Spain.
    Chaves FJ; Puig O; García-Sogo M; Real J; Gil JV; Ascaso J; Carmena R; Armengod ME
    Clin Genet; 1996 Jul; 50(1):28-35. PubMed ID: 8891383
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Chinese homozygote of familial hypercholesterolemia: identification of a novel C263R mutation in the LDL receptor gene.
    Wang D; Wu B; Li Y; Heng W; Zhong H; Mu Y; Wang J
    J Hum Genet; 2001; 46(3):152-4. PubMed ID: 11310584
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Polymorphisms of the low-density lipoprotein receptor gene in Brazilian individuals with heterozygous familial hypercholesterolemia.
    Salazar LA; Cavalli SA; Hirata MH; Diament J; Forti N; Giannini SD; Nakandakare ER; Bertolami MC; Hirata RD
    Braz J Med Biol Res; 2000 Nov; 33(11):1301-4. PubMed ID: 11050659
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in a Spanish population.
    Cenarro A; Jensen HK; Civeira F; Casao E; Ferrando J; González-Bonillo J; Pocoví M; Gregersen N
    Clin Genet; 1996 Apr; 49(4):180-5. PubMed ID: 8828982
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism method.
    Loux N; Saint-Jore B; Collod G; Dairou F; Benlian P; Truffert J; Dastugue B; Douste-Blazy P; de Gennes JL; Junien C
    Hum Mutat; 1992; 1(4):325-32. PubMed ID: 1301940
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A new polymorphism in exon 11 of the LDL receptor gene in healthy people and in familial hypercholesterolemia subjects.
    Leren TP; Solberg K; Røsby O; Rødningen OK; Tonstad S; Ose L; Berg K
    Clin Genet; 1992 Nov; 42(5):224-8. PubMed ID: 1486698
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Polymorphic haplotypes and recombination rates at the LDL receptor gene locus in subjects with and without familial hypercholesterolemia who are from different populations.
    Miserez AR; Schuster H; Chiodetti N; Keller U
    Am J Hum Genet; 1993 Apr; 52(4):808-26. PubMed ID: 8096361
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TaqI polymorphism in the LDL receptor gene and a TaqI 1.5-kb band associated with familial hypercholesterolemia.
    Yamakawa K; Okafuji T; Iwamura Y; Yuzawa K; Satoh J; Hattori N; Yamanouchi Y; Yanagi H; Kawai K; Tsuchiya S
    Hum Genet; 1988 Sep; 80(1):1-5. PubMed ID: 2901393
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low-density-lipoprotein receptor gene and PvuII polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment.
    Vuorio AF; Ojala JP; Sarna S; Turtola H; Tikkanen MJ; Kontula K
    J Intern Med; 1995 Jan; 237(1):43-8. PubMed ID: 7830029
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [DNA analysis in heterozygotes in familial hypercholesterolemia].
    Horínek A; Slézka V; Sobra J; Ceska R
    Cas Lek Cesk; 1995 Apr; 134(8):234-9. PubMed ID: 7758080
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The usefulness of three biallelic restriction fragment length polymorphisms versus a polymorphic dinucleotide tandem repeat polymorphism at the low-density-lipoprotein receptor gene locus for diagnosis of familial hypercholesterolemia.
    Weiss N; Gudnasson V; Ostwald P; Humphries S; Schuster H; Keller C
    Dis Markers; 1997 Nov; 13(3):141-51. PubMed ID: 9405927
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spectrum of LDL receptor gene mutations in Denmark: implications for molecular diagnostic strategy in heterozygous familial hypercholesterolemia.
    Jensen HK; Jensen LG; Meinertz H; Hansen PS; Gregersen N; Faergeman O
    Atherosclerosis; 1999 Oct; 146(2):337-44. PubMed ID: 10532689
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of Scotland.
    Lee WK; Haddad L; Macleod MJ; Dorrance AM; Wilson DJ; Gaffney D; Dominiczak MH; Packard CJ; Day IN; Humphries SE; Dominiczak AF
    J Med Genet; 1998 Jul; 35(7):573-8. PubMed ID: 9678702
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Relationship between changes in activities of low density lipoprotein receptor and gene mutation in familial hypercholesterolemia].
    Pang Q; Li M; Hu W; Chen Q; Li X; Fan L
    Zhonghua Nei Ke Za Zhi; 2002 Oct; 41(10):667-70. PubMed ID: 12485531
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Common mutations in the low-density-lipoprotein-receptor gene causing familial hypercholesterolemia in the Japanese population.
    Maruyama T; Miyake Y; Tajima S; Harada-Shiba M; Yamamura T; Tsushima M; Kishino B; Horiguchi Y; Funahashi T; Matsuzawa Y
    Arterioscler Thromb Vasc Biol; 1995 Oct; 15(10):1713-8. PubMed ID: 7583548
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus.
    Kotze MJ; Langenhoven E; Retief AE; Seftel HC; Henderson HE; Weich HF
    J Med Genet; 1989 Apr; 26(4):255-9. PubMed ID: 2565980
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Familial hypercholesterolemia from the aspect of DNA analysis].
    Horínek A; Sobra J; Ceska R; Paulasová P
    Vnitr Lek; 1993 Oct; 39(10):946-50. PubMed ID: 7901941
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Screening for point mutations in exon 10 of the low density lipoprotein receptor gene by analysis of single-strand conformation polymorphisms: detection of a nonsense mutation-FH469-->Stop.
    Leren TP; Solberg K; Rødningen OK; Røsby O; Tonstad S; Ose L; Berg K
    Hum Genet; 1993 Aug; 92(1):6-10. PubMed ID: 8103503
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial hypercholesterolemia study in Sardinia using 6 LDLR polymorphic markers based on PCR.
    Orrù S; Pintor S; Loizedda A; Giuressi E; Murru R; Casula M; Carcassi C; Deiana L; Contu L
    Am J Med Genet; 2000 Mar; 91(1):34-8. PubMed ID: 10751086
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.