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Data reveal that necdin promotes mitochondrial biogenesis through stabilization of endogenous PGC-1alpha to exert neuroprotection against mitochondrial insults.
Our data suggest that necdin suppresses PIAS1 both by inhibiting SUMO E3 ligase activity and by promoting ubiquitin-dependent degradation.
Necdin is a candidate downstream effector for Galphao (show GNAO1 Proteins).
Myc (show MYC Proteins) overexpression in the cpk kidney results from the dysregulation of the cystin-necdin regulatory complex and c-Myc (show MYC Proteins), in turn, contributes to cystogenesis in the cpk mouse.
Antagonistic interplay between necdin and Bmi1 (show BMI1 Proteins) controls proliferation of neural precursor cells in the embryonic mouse neocortex.
using several mouse models, we reveal a competition between non-imprinted Ndn promoters which results in monoallelic (paternal or maternal) Ndn expression, suggesting that Ndn allelic exclusion occurs in the absence of imprinting regulation.
oxygen tension regulates the necdin protein level in NSCs through HIF-2alpha (show EPAS1 Proteins)-mediated proteasomal
necdin exerts its pro-survival activity by counteracting the action of the pro-apoptotic protein Cell Cycle Apoptosis Regulatory Protein (CCAR1/CARP1)
Necdin-null adult hematopoietic stem cells are less quiescent and more proliferative than normal hematopoietic stem cells, demonstrating the similar role of necdin and p53 (show TP53 Proteins) in promoting hematopoietic stem cells quiescence during steady-state conditions.
necdin has multiple roles within protein complexes in different subcellular compartments, and indicate that it can utilize multiple karyopherin-dependent pathways to modulate its localization.
In the skeletal muscle of neonate pigs, both NECD and SNRPN (show SNRPN Proteins) were maternally imprinted, while UBE3A (show ube3a Proteins) was not imprinted.
Imprinting analysis showed that NDN and MAGEL2 (show MAGEL2 Proteins) are paternally expressed in all tissues of pig where the genes were expressed as in human and mouse.
Germline single nucleotide polymorphism in necdin gene is associated with breast cancer.
NDN and CD1A (show CD1A Proteins) are novel prognostic methylation markers in patients with head and neck squamous carcinomas
Necdin expression declined during replicative aging of IMR90 primary human fibroblasts or after induction of premature senescence.Showed that in normal human cells, Necdin expression mimicked the effect of p53 (show TP53 Proteins) inactivation by increasing radioresistance.
Hypermethylation and mutation of necdin is associated with neoplasms.
In pre-adipocytes, necdin over-expression inhibits adipogenesis, while reducing necdin levels enhances adipogenic differentiation in tissue culture cell
Necdin, a negative growth regulator,identified as a novel STAT3 (show STAT3 Proteins) target gene, whose expression is down-regulated at the mRNA and protein levels when STAT3 (show STAT3 Proteins) is constitutively active.
Necdin is implicated through the TNF (show TNF Proteins)-receptor 1 pathway in the developmental death of motoneuron
rare variant of necdin (p.V318A) was described in a family with Kallmann syndrome Familial segregation and in vitro analysis suggested that this non-synonymous variant did not have a direct causative role in hypogonadism phenotype.
This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons.
, Prader-Willi syndrome chromosome region
, necdin homolog