rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
10
|
pubmed:dateCreated |
1998-12-23
|
pubmed:abstractText |
Fanconi's anemia (FA) is a rare autosomal recessive syndrome characterized by skeletal abnormalities, late onset bone marrow failure and susceptibility to neoplasias. Reduced defense against oxidative stress is thought to be one of the cell damaging mechanisms. We investigated in vitro the effects of oxidative stress on red blood cells (RBC) and on hematopoietic progenitor growth of normal donors and of FA patients.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0390-6078
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
83
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
868-74
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:9830794-Adolescent,
pubmed-meshheading:9830794-Adult,
pubmed-meshheading:9830794-Cells, Cultured,
pubmed-meshheading:9830794-Child,
pubmed-meshheading:9830794-Child, Preschool,
pubmed-meshheading:9830794-Erythrocytes,
pubmed-meshheading:9830794-Fanconi Anemia,
pubmed-meshheading:9830794-Female,
pubmed-meshheading:9830794-Hematopoietic Stem Cells,
pubmed-meshheading:9830794-Humans,
pubmed-meshheading:9830794-Hydrogen Peroxide,
pubmed-meshheading:9830794-Male,
pubmed-meshheading:9830794-Oxidants,
pubmed-meshheading:9830794-Oxidative Stress
|
pubmed:year |
1998
|
pubmed:articleTitle |
Fanconi's anemia cells are relatively resistant to H2O2-induced damage.
|
pubmed:affiliation |
Division of Hematology, Federico II University Medical School, Naples, Italy.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|