about
MxA overexpression reveals a common genetic link in four Fanconi anemia complementation groupsFanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complexInduction of Fanconi anemia cellular phenotype in human 293 cells by overexpression of a mutant FAC alleleEvidence for at least eight Fanconi anemia genesA physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCAFunctional activity of the fanconi anemia protein FAA requires FAC binding and nuclear localization.Oesophageal atresia, VACTERL association: Fanconi's anaemia related spectrum of anomaliesThe fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation.Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells.Fanconi Anemia: A DNA repair disorder characterized by accelerated decline of the hematopoietic stem cell compartment and other features of aging.Cytoprotective effect of honey against chromosomal breakage in fanconi anemia patients in vitro.Structure and function of the human Werner syndrome gene promoter: evidence for transcriptional modulation.Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transfer.Diagnosis of Fanconi's Anemia by Diepoxybutane Analysis in Children from Serbia.
P2860
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P1343
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P2860
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Fanconi anemia and novel strategies for therapy.
@en
type
label
Fanconi anemia and novel strategies for therapy.
@en
prefLabel
Fanconi anemia and novel strategies for therapy.
@en
P2093
P1433
P1476
Fanconi anemia and novel strategies for therapy.
@en
P2093
P304
P407
P577
1994-12-01T00:00:00Z