Literature DB >> 996788

Polyamine metabolism in cystic fibrosis.

O M Rennert, J Frias, J B Shukla.   

Abstract

Increased blood levels of spermidine and an increased spermidine/spermine ratio is documented in 31 patients with cystic fibrosis (CF). Some 29 percent of CF patients overlap with the control group. An abnormality of urinary free polyamines or their metabolic derivatives related to electrolyte transport, serum ciliostatic factors, and the autonomic nervous system are elaborated upon.

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Year:  1976        PMID: 996788

Source DB:  PubMed          Journal:  Tex Rep Biol Med        ISSN: 0040-4675


  3 in total

1.  Pattern of blood polyamines in healthy subjects from infancy to the adult age.

Authors:  A Casti; G Orlandini; N Reali; F Bacciottini; M Vanelli; S Bernasconi
Journal:  J Endocrinol Invest       Date:  1982 Jul-Aug       Impact factor: 4.256

2.  Inhibition of protein kinase CK2 closes the CFTR Cl channel, but has no effect on the cystic fibrosis mutant deltaF508-CFTR.

Authors:  Kate J Treharne; Zhe Xu; Jeng-Haur Chen; O Giles Best; Diane M Cassidy; Dieter C Gruenert; Péter Hegyi; Michael A Gray; David N Sheppard; Karl Kunzelmann; Anil Mehta
Journal:  Cell Physiol Biochem       Date:  2009-11-04

3.  L-ornithine derived polyamines in cystic fibrosis airways.

Authors:  Hartmut Grasemann; Darakhshanda Shehnaz; Masahiro Enomoto; Michael Leadley; Jaques Belik; Felix Ratjen
Journal:  PLoS One       Date:  2012-10-05       Impact factor: 3.240

  3 in total

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