Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene.
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Aldehyde dehydrogenase 2 in aplastic anemia, Fanconi anemia and hematopoietic stem cellsFanconi anemia protein FANCD2 is activated by AICAR, a modulator of AMPK and cellular energy metabolismA never-ending story: the steadily growing family of the FA and FA-like genesElucidation of the Fanconi Anemia Protein Network in Meiosis and Its Function in the Regulation of Histone Modifications.Bloom syndrome complex promotes FANCM recruitment to stalled replication forks and facilitates both repair and traverse of DNA interstrand crosslinksMaintenance of genome stability by Fanconi anemia proteins.The prognostic value of DNA damage level in peripheral blood lymphocytes of chemotherapy-naïve patients with germ cell cancer.Overlooked FANCD2 variant encodes a promising, portent tumor suppressor, and alternative polyadenylation contributes to its expression.Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia.Hematopoietic cell transplantation in Fanconi anemia: current evidence, challenges and recommendations.Recent insights into the molecular basis of Fanconi anemia: genes, modifiers, and drivers.Involvement of FANCD2 in Energy Metabolism via ATP5α.A strategy for molecular diagnostics of Fanconi anemia in Brazilian patients.A germline FANCA alteration that is associated with increased sensitivity to DNA damaging agents.V(D)J recombination process and the Pre-B to immature B-cells transition are altered in Fanca(-/-) mice.De novo chromosome 7q36.1q36.2 triplication in a child with developmental delay, growth failure, distinctive facial features, and multiple congenital anomalies: a case reportBiallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia.Loss of the homologous recombination gene rad51 leads to Fanconi anemia-like symptoms in zebrafish.Persistent response of Fanconi anemia haematopoietic stem and progenitor cells to oxidative stress.Therapeutic gene editing in CD34+ hematopoietic progenitors from Fanconi anemia patients.Using family history forms in pediatric oncology to identify patients for genetic assessment.FANCI and FANCD2 have common as well as independent functions during the cellular replication stress response.Reduced Cdc42 Activity Compromises Hematopoiesis-Supportive Function Of Fanconi Anemia Mesenchymal Stromal Cells.Icraiin improves Fanconi anemia hematopoietic stem cell function through SIRT6-mediated NF-kappa B inhibition.Recent advances in understanding hematopoiesis in Fanconi Anemia.Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.Coordination of the recruitment of the FANCD2 and PALB2 Fanconi anemia proteins by an ubiquitin signaling network.Studies in an Early Development Window Unveils a Severe HSC Defect in both Murine and Human Fanconi Anemia
P2860
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P2860
Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Complementation of hypersensit ...... CC2 is a Fanconi anaemia gene.
@en
type
label
Complementation of hypersensit ...... CC2 is a Fanconi anaemia gene.
@en
prefLabel
Complementation of hypersensit ...... CC2 is a Fanconi anaemia gene.
@en
P2093
P2860
P1476
Complementation of hypersensit ...... CC2 is a Fanconi anaemia gene.
@en
P2093
Anna Jankowska
Constanze Wiek
Elizabeth L Virts
Helmut Hanenberg
Jung-Young Park
Mohamed Othman
Paul R Andreassen
Sujata C Chakraborty
P2860
P304
P356
10.1136/JMEDGENET-2016-103847
P407
P577
2016-05-20T00:00:00Z