Oxidative energy deficiency. II. Human achondroplasia

B. Mackler, B. Haynes, A. R. Inamdar, L. R. Pedegana, J. G. Hall, M. M. Cohen

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19 Citations (Scopus)

Résumé

Defective oxidative energy formation (with decreased phosphorylation possibly occurring at Site I of phosphorylation, the NADH dehydrogenase region of the terminal respiratory system) has been demonstrated in mitochondrial preparations isolated from muscle biopsy specimens from human subjects with classical achondroplasia.

Langue d'origineEnglish
Pages (de-à)885-888
Nombre de pages4
JournalArchives of Biochemistry and Biophysics
Volume159
Numéro de publication2
DOI
Statut de publicationPublished - déc. 1973
Publié à l'externeOui

Note bibliographique

Funding Information:
’ This work was supported in part by Grants HL 03437, Hl) 06346, HI) 0.5961, and a career development award (,M.M.C.) from the National Institutes of Healt,h, and Grant CRBS-27.5 from the National Foundation. A portion of this work was conducted through the Clinical Research Center facility of the University of Washington, srlpported by the NIH Grant RR-X.

ASJC Scopus Subject Areas

  • Biophysics
  • Biochemistry
  • Molecular Biology

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