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Low NBS1 expression is associated with low-grade epithelial ovarian cancer.
although recruitment of the MRE11 (显示 MRE11A ELISA试剂盒)-RAD50 (显示 RAD50 ELISA试剂盒)-NBS1 (MRN) DSB-sensing complex to viral genomes and activation of the ATM (显示 ATM ELISA试剂盒) kinase can promote KSHV replication, proteins involved in nonhomologous end joining (NHEJ) repair restrict amplification of viral DNA.
Data suggest HSP90AA1-dependent regulation of ATM-NBN-CHK2 and ATR-CHK1 axes influences cells capability to repair double-stranded DNA damage; mechanisms include phosphorylation, polyubiquitination, and proteasomal degradation/proteolysis. (HSP90AA1 = heat shock protein 90kDa alpha; ATM = ataxia telangiectasia mutated protein; NBN = nibrin; CHK = checkpoint kinase; ATR = ataxia telangiectasia and Rad3 related kinase)
Mre11 (显示 MRE11A ELISA试剂盒)-Rad50 (显示 RAD50 ELISA试剂盒)-Nbs1 complex initiates DNA double strand break repair.
Phosphorylation status of NBS1 determines how dysfunctional telomeres are repaired.
The results illuminate the important role of Nbs1 and CtIP (显示 RBBP8 ELISA试剂盒) in determining the substrates and consequences of human Mre11 (显示 MRE11A ELISA试剂盒)/Rad50 (显示 RAD50 ELISA试剂盒) nuclease (显示 DCLRE1C ELISA试剂盒) activities on protein-DNA lesions.
The Nbs1 homologs that promote herpes simplex virus 1 infection also interact with the herpes simplex virus 1 ICP0 protein.
The CC genotype of NBS1 Glu185Gln may increase lung cancer risk only for males and smokers and may serve as a practical marker for early detective and predictive purposes of lung cancer
surmise that the higher fertility of female c.657del5 carriers reflects a lower miscarriage rate in these women, thereby reflecting the role of the NBN gene product, nibrin, in the repair of DNA double strand breaks and their processing in immune gene rearrangements, telomere maintenance, and meiotic recombination
although Mre11 (显示 MRE11A ELISA试剂盒) is required for efficient HR-dependent repair of ionizing-radiation-induced DSBs, Mre11 (显示 MRE11A ELISA试剂盒) is largely dispensable for DSB resection in both chicken DT40 and human TK6 B cell lines.
the essential role of Nbs1 is via its interaction with Mre11 (显示 MRE11A ELISA试剂盒) and that most of the Nbs1 protein is dispensable for Mre11 (显示 MRE11A ELISA试剂盒) complex functions and suggest that Mre11 (显示 MRE11A ELISA试剂盒) and Rad50 (显示 RAD50 ELISA试剂盒) directly activate ATM (显示 ATM ELISA试剂盒).
Low NBS1 expression is associated with B-cell lymphomas.
findings show that NBS1 is crucial for macrophage function during normal aging
TRIP13 (显示 TRIP13 ELISA试剂盒)-deficient spermatocytes also progress to an H1t (显示 HIST1H1T ELISA试剂盒)-positive stage if ATM (显示 ATM ELISA试剂盒) activity is attenuated by hypomorphic mutations in Mre11 (显示 MRE11A ELISA试剂盒) or Nbs1 or by elimination of the ATM (显示 ATM ELISA试剂盒)-effector kinase CHK2 (显示 CHEK2 ELISA试剂盒)
In the absence of wild type nibrin, the repair of spontaneous errors, presumably arising during DNA replication, makes a major contribution to the basal mutation rate.
Nbs1 mutants initially accumulate replication intermediate, not DSBs.
This report showed that ATM (显示 ATM ELISA试剂盒)-Chk2 (显示 CHEK2 ELISA试剂盒)-P53 (显示 TP53 ELISA试剂盒) signaling pathway and the AKT (显示 AKT1 ELISA试剂盒)/mTOR (显示 FRAP1 ELISA试剂盒) signaling pathway are responsible for the enhanced apoptosis of the Nbn-deficient mature oligodendrocytes.
JNK (显示 MAPK8 ELISA试剂盒) signaling and ATR (显示 ATR ELISA试剂盒) signaling are likely to converge to regulate the cerebellar apoptosis of newborn Nbn-deficient mice.
Nbn and Atm (显示 ATM ELISA试剂盒) collaborate to prevent DSB accumulation and apoptosis during development in a tissue- and developmental stage-specific manner.
Mutations in this gene are associated with Nijmegen breakage syndrome, an autosomal recessive chromosomal instability syndrome characterized by microcephaly, growth retardation, immunodeficiency, and cancer predisposition. The encoded protein is a member of the MRE11/RAD50 double-strand break repair complex which consists of 5 proteins. This gene product is thought to be involved in DNA double-strand break repair and DNA damage-induced checkpoint activation.
, Nijmegen breakage syndrome 1 (nibrin)
, cell cycle regulatory protein p95
, p95 protein of the MRE11/RAD50 complex
, nijmegen breakage syndrome protein 1 homolog