You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/64248
Title: 
Sister-chromatid exchanges in β-thalassaemic patients under conditions of in vivo and in vitro depletion of folic acid
Author(s): 
Institution: 
Universidade Estadual Paulista (UNESP)
ISSN: 
0165-7992
Abstract: 
In order to investigate the effect of folate depletion, lymphocyte sister-chromatid exchange (SCE) rates were compared among homozygous β-thalassaemic patients with low folic acid levels, heterozygous β-thalassaemic patients with normal folate levels and healthy persons with normal haemoglobin, in cultures with both normal and depleted folate conditions. Significantly higher SCE rates were found in homozygous patients in all assays, but the in vitro folate depletion did not induce an increase in SCE frequency in any group.
Issue Date: 
2-Jul-1992
Citation: 
Mutation Research - Mutation Research Letters, v. 282, n. 3, p. 213-217, 1992.
Time Duration: 
213-217
Keywords: 
  • β-Thalassaemia
  • Culture conditions
  • Follic acid
  • Sister-chromatid exchange
  • folic acid
  • beta thalassemia
  • clinical article
  • controlled study
  • heterozygote
  • homozygote
  • human
  • human cell
  • lymphocyte culture
  • priority journal
  • sister chromatid exchange
  • Adolescent
  • Adult
  • Analysis of Variance
  • Cells, Cultured
  • Child
  • Child, Preschool
  • Folic Acid Deficiency
  • Human
  • Infant
  • Lymphocytes
  • Sister Chromatid Exchange
  • Support, Non-U.S. Gov't
  • Thalassemia
Source: 
http://dx.doi.org/10.1016/0165-7992(92)90098-3
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/64248
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.