Literature DB >> 2377494

Dinucleotide repeat polymorphism at the 3' end of the LDL receptor gene.

G Zuliani1, H H Hobbs.   

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Year:  1990        PMID： 2377494      PMCID： PMC331238          DOI： 10.1093/nar/18.14.4300

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  2 in total

1.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

Authors:  R K Saiki; D H Gelfand; S Stoffel; S J Scharf; R Higuchi; G T Horn; K B Mullis; H A Erlich
Journal:  Science       Date:  1988-01-29       Impact factor: 47.728

2.  Human genes involved in cholesterol metabolism: chromosomal mapping of the loci for the low density lipoprotein receptor and 3-hydroxy-3-methylglutaryl-coenzyme A reductase with cDNA probes.

Authors:  V Lindgren; K L Luskey; D W Russell; U Francke
Journal:  Proc Natl Acad Sci U S A       Date:  1985-12       Impact factor: 11.205
  2 in total
  11 in total

1.  Detection of four new TaqI alleles with probe St14-1.

Authors:  S Casares; M Olivera; M Vinuesa; J M Rodriguez
Journal:  Nucleic Acids Res       Date:  1991-12-11       Impact factor: 16.971

2.  Multilocus genetic determinants of LDL particle size in coronary artery disease families.

Authors:  J I Rotter; X Bu; R M Cantor; C H Warden; J Brown; R J Gray; P J Blanche; R M Krauss; A J Lusis
Journal:  Am J Hum Genet       Date:  1996-03       Impact factor: 11.025

3.  A gene for universal congenital alopecia maps to chromosome 8p21-22.

Authors:  M M Nöthen; S Cichon; I R Vogt; S Hemmer; R Kruse; M Knapp; T Höller; M Faiyaz ul Haque; S Haque; P Propping; M Ahmad; M Rietschel
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

4.  A HaeIII polymorphism in the 3' untranslated region of the low density lipoprotein receptor (LDLR) gene.

Authors:  J A Cavanaugh; S Easteal
Journal:  Nucleic Acids Res       Date:  1991-12-11       Impact factor: 16.971

5.  European workshop on LDL receptor defects. European Working Group on Familial Hypercholesterolaemia.

Authors:  H Schuster; S Humphries
Journal:  Clin Investig       Date:  1994-11

6.  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.

Authors:  S Humphries; L King-Underwood; V Gudnason; M Seed; S Delattre; V Clavey; J C Fruchart
Journal:  J Med Genet       Date:  1993-04       Impact factor: 6.318

7.  Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype.

Authors:  H Allayee; B E Aouizerat; R M Cantor; G M Dallinga-Thie; R M Krauss; C D Lanning; J I Rotter; A J Lusis; T W de Bruin
Journal:  Am J Hum Genet       Date:  1998-08       Impact factor: 11.025

8.  Polymorphisms at cholesterol 7alpha-hydroxylase, apolipoproteins B and E and low density lipoprotein receptor genes in patients with gallbladder stone disease.

Authors:  Zhao-Yan Jiang; Tian-Quan Han; Guang-Jun Suo; Dian-Xu Feng; Sheng Chen; Xing-Xing Cai; Zhi-Hong Jiang; Jun Shang; Yi Zhang; Yu Jiang; Sheng-Dao Zhang
Journal:  World J Gastroenterol       Date:  2004-05-15       Impact factor: 5.742

9.  Linkage of atherogenic lipoprotein phenotype to the low density lipoprotein receptor locus on the short arm of chromosome 19.

Authors:  P M Nishina; J P Johnson; J K Naggert; R M Krauss
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-15       Impact factor: 11.205

10.  Familial ligand-defective apolipoprotein B. Identification of a new mutation that decreases LDL receptor binding affinity.

Authors:  C R Pullinger; L K Hennessy; J E Chatterton; W Liu; J A Love; C M Mendel; P H Frost; M J Malloy; V N Schumaker; J P Kane
Journal:  J Clin Invest       Date:  1995-03       Impact factor: 14.808
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