Literature DB >> 2931552

Vitamins: an evolutionary perspective.

C R Scriver.   

Abstract

Access to vitamins and the genetic endownment to utilize them maintain vitamin-dependent metabolic homeostasis in heterotrophs. Whereas the extent of adverse nutritional experiences has declined in modern human societies, phenocopies of deficiency diseases persist; accordingly, they have high heritability. The "vitamin-responsive hereditary metabolic diseases" identify DNA that specifies conserved apoenzyme domains interacting with coenzyme and the cellular processes providing access to coenzymes. Could heterozygosity at those loci also be a determinant of disease (or health) under certain circumstances?

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Year:  1985        PMID: 2931552     DOI: 10.1007/BF01800651

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  10 in total

Review 1.  Synthesis and some major functions of vitamin C in animals.

Authors:  I B Chatterjee; A K Majumder; B K Nandi; N Subramanian
Journal:  Ann N Y Acad Sci       Date:  1975-09-30       Impact factor: 5.691

2.  Prevention of the Wernicke-Korsakoff syndrome: a cost-benefit analysis.

Authors:  B S Centerwall; M H Criqui
Journal:  N Engl J Med       Date:  1978-08-10       Impact factor: 91.245

Review 3.  Vitamin-responsive inherited metabolic disorders.

Authors:  L E Rosenberg
Journal:  Adv Hum Genet       Date:  1976

4.  Vitamin-responsive inborn errors of metabolism.

Authors:  C R Scriver
Journal:  Metabolism       Date:  1973-10       Impact factor: 8.694

5.  On the heritability of rickets, a common disease (Mendel, mammals and phosphate).

Authors:  C R Scriver; H S Tenenhouse
Journal:  Johns Hopkins Med J       Date:  1981-11

6.  Can some people synthesize ascorbic acid?

Authors:  M Cummings
Journal:  Am J Clin Nutr       Date:  1981-02       Impact factor: 7.045

7.  Na+-dependent, potential-sensitive L-ascorbate transport across brush border membrane vesicles from kidney cortex.

Authors:  G Toggenburger; M Häusermann; B Mütsch; G Genoni; M Kessler; F Weber; D Hornig; B O'Neill; G Semenza
Journal:  Biochim Biophys Acta       Date:  1981-09-07

8.  Abnormality of a thiamine-requiring enzyme in patients with Wernicke-Korsakoff syndrome.

Authors:  J P Blass; G E Gibson
Journal:  N Engl J Med       Date:  1977-12-22       Impact factor: 91.245

9.  Thiamin-responsive maple-syrup-urine disease: decreased affinity of the mutant branched-chain alpha-keto acid dehydrogenase for alpha-ketoisovalerate and thiamin pyrophosphate.

Authors:  D T Chuang; L S Ku; R P Cox
Journal:  Proc Natl Acad Sci U S A       Date:  1982-05       Impact factor: 11.205

10.  The natural history of the inherited methylmalonic acidemias.

Authors:  S M Matsui; M J Mahoney; L E Rosenberg
Journal:  N Engl J Med       Date:  1983-04-14       Impact factor: 91.245

  10 in total
  2 in total

Review 1.  Human neural tube defects: developmental biology, epidemiology, and genetics.

Authors:  Eric R Detrait; Timothy M George; Heather C Etchevers; John R Gilbert; Michel Vekemans; Marcy C Speer
Journal:  Neurotoxicol Teratol       Date:  2005-03-05       Impact factor: 3.763

Review 2.  Vitamin neurotoxicity.

Authors:  S R Snodgrass
Journal:  Mol Neurobiol       Date:  1992       Impact factor: 5.590

  2 in total

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