Literature DB >> 8364820

No prescription for despair.

A Robinson.   

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Year:  1993        PMID： 8364820      PMCID： PMC1485986     

Source DB:  PubMed          Journal:  CMAJ        ISSN： 0820-3946            Impact factor:   8.262


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  8 in total

Review 1.  The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane protein.

Authors:  H H Hobbs; D W Russell; M S Brown; J L Goldstein
Journal:  Annu Rev Genet       Date:  1990       Impact factor: 16.830

2.  A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French Canadians.

Authors:  Y Ma; H E Henderson; V Murthy; G Roederer; M V Monsalve; L A Clarke; T Normand; P Julien; C Gagné; M Lambert
Journal:  N Engl J Med       Date:  1991-06-20       Impact factor: 91.245

3.  A major insertion accounts for a significant proportion of mutations underlying human lipoprotein lipase deficiency.

Authors:  S Langlois; S Deeb; J D Brunzell; J J Kastelein; M R Hayden
Journal:  Proc Natl Acad Sci U S A       Date:  1989-02       Impact factor: 11.205

4.  Hepatic lipase deficiency. Clinical, biochemical, and molecular genetic characteristics.

Authors:  R A Hegele; J A Little; C Vezina; G F Maguire; L Tu; T S Wolever; D J Jenkins; P W Connelly
Journal:  Arterioscler Thromb       Date:  1993-05

Review 5.  Phenotypic variation of mutations in the human lipoprotein-lipase gene.

Authors:  M R Hayden; J J Kastelein; H Funke; J D Brunzell; Y Ma
Journal:  Biochem Soc Trans       Date:  1993-05       Impact factor: 5.407

6.  Homozygous familial hypercholesterolemia among French Canadians in Québec Province.

Authors:  S Moorjani; M Roy; C Gagné; J Davignon; D Brun; M Toussaint; M Lambert; L Campeau; S Blaichman; P Lupien
Journal:  Arteriosclerosis       Date:  1989 Mar-Apr

7.  Incomplete fatty acid oxidation. The production and epimerization of 3-hydroxy fatty acids.

Authors:  S J Jin; C L Hoppel; K Y Tserng
Journal:  J Biol Chem       Date:  1992-01-05       Impact factor: 5.157

8.  A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries.

Authors:  M V Monsalve; H Henderson; G Roederer; P Julien; S Deeb; J J Kastelein; L Peritz; R Devlin; T Bruin; M R Murthy
Journal:  J Clin Invest       Date:  1990-09       Impact factor: 14.808
  8 in total

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