Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype
about
MxA overexpression reveals a common genetic link in four Fanconi anemia complementation groupsHigh frequency of large intragenic deletions in the Fanconi anemia group A gene.The Fanconi anemia group E gene, FANCE, maps to chromosome 6pFanconi 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 alleleSequence variation in the Fanconi anemia gene FAAEvidence for at least eight Fanconi anemia genesA physical complex of the Fanconi anemia proteins FANCG/XRCC9 and FANCAAnalysis of baseline and cisplatin-inducible gene expression in Fanconi anemia cells using oligonucleotide-based microarrays.A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51A never-ending story: the steadily growing family of the FA and FA-like genesFunctional activity of the fanconi anemia protein FAA requires FAC binding and nuclear localization.Interstrand cross-links induce DNA synthesis in damaged and undamaged plasmids in mammalian cell extracts.Mutations of the Fanconi anemia group A gene (FAA) in Italian patients.Evidence for subcomplexes in the Fanconi anemia pathway.A locus for Fanconi anemia on 16q determined by homozygosity mapping.The fanconi anemia pathway requires FAA phosphorylation and FAA/FAC nuclear accumulation.Investigation of FANCA gene in Fanconi anaemia patients in Iran.Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.Cytoplasmic localization of FAC is essential for the correction of a prerepair defect in Fanconi anemia group C cells.FANCJ protein is important for the stability of FANCD2/FANCI proteins and protects them from proteasome and caspase-3 dependent degradation.Complementation analysis in Fanconi anemia: assignment of the reference FA-H patient to group ASubtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transfer.Acquired cross-linker resistance associated with a novel spliced BRCA2 protein variant for molecular phenotyping of BRCA2 disruption.Noncomplementation of radiation-induced chromosome aberrations in ataxia-telangiectasia/ataxia-telangiectasia-variant heterodikaryons.
P2860
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P1343
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P2860
Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype
description
1995 nî lūn-bûn
@nan
1995 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1995 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
name
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@ast
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@en
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@nl
type
label
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@ast
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@en
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@nl
prefLabel
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@ast
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@en
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@nl
P2093
P4510
P1433
P1476
Classification of Fanconi anem ...... ce for a fifth genetic subtype
@en
P2093
A B Oostra
C G van Berkel
J R Lo ten Foe
M A Rooimans
M Buchwald
R D Wegner
T Schroeder-Kurth
P304
P407
P577
1995-09-15T00:00:00Z