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NOVA1 encodes a neuron-specific RNA-binding protein, a member of the Nova family of paraneoplastic disease antigens, that is recognized and inhibited by paraneoplastic antibodies. Additionally we are shipping NOVA1 Antibodies (76) and many more products for this protein.
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overexpression of miR (show MLXIP Proteins)-203a-3p leads to a decrease of NOVA1, counter-balanced by an increase of IKAP (show IKBKAP Proteins), supporting a potential interaction between NOVA1 and IKAP (show IKBKAP Proteins).
NOVA1 suppression was frequently noted in the gastric cancer microenvironment, and attenuated NOVA1 expression in tumor cells was associated with tumor progression and poor prognosis.
Nova1 interacts with GABAARgamma2 not only in the central nervous system but also in hepatocellular carcinoma. Nova1's potential mechanism as an oncogene (show RAB1A Proteins) may due to its interaction with GABAA (show GABRg1 Proteins) Rgamma2.
Loss of NOVA1 is associated with gastric cancer.
Quantitative proteomic analysis was performed to help elucidate a molecular distinction between glioblastoma and oligodendroglioma; analysis showed HSPB1 (show HSPB1 Proteins) and NOVA1 to be discriminating factors.
Data indicate RNA binding protein (show PTBP1 Proteins) NOVA1 as a target of microRNA miR (show MLXIP Proteins)-339.
MiR (show MLXIP Proteins)-181b-5p is a tumor suppressor in astrocytoma that inhibits tumor progression by targeting NOVA1.
High expression of NOVA1 correlates with poor prognosis in hepatocellular carcinoma.
a regulation of LEDGF (show PSIP1 Proteins) interaction with chromatin by cellular partners of its PWWP domain could be involved in several processes linked to LEDGF (show PSIP1 Proteins) tethering properties, such as lentiviral integration, DNA repair or transcriptional regulation
Gene silencing and overexpression of the nELAV member HuD (show ELAVL4 Proteins) in motoneuronal NSC34 cells indicate that Nova1 mRNA stability and translation are positively and strongly controlled by the nELAV proteins
Together, these results demonstrate that the production of DCC (show DCC Proteins) splice variants controlled by NOVA (show HNRNPK Proteins) has a crucial function during many stages of commissural neuron development.
Phenotypic analysis of the NOVA (show HNRNPK Proteins)-deficient mice demonstrated increased adipose tissue thermogenesis and improved glycemia.
RBM4a (show RBM4 Proteins) ablation enhanced the relative level of exon 4-excluded neuro-oncological ventral antigen 1 (Nova1(-4)) transcripts, which were predominantly generated in embryonic BAs
identify Nova-1 and hnRNP M (show HNRNPM Proteins) as D2R (show DRD2 Proteins) pre-mRNA-binding proteins and show their antagonistic role in the alternative splicing of D2R (show DRD2 Proteins) pre-mRNA.
integrative network revealed combinatorial regulation by Nova (show HNRNPK Proteins) and the neuronal splicing factor (show SLU7 Proteins) Fox, interplay between phosphorylation and splicing, and potential links to neurologic disease
Nova (show HNRNPK Proteins) regulates GABA(A) receptor gamma2 alternative splicing via a distal downstream UCAU-rich intronic splicing enhancer
CLIP (cross-linking and immunoprecipitation) reveals Nova (show HNRNPK Proteins) coordinately regulates a biologically coherent set of RNAs encoding multiple components of the inhibitory synapse, an observation that may relate to the cause of abnormal motor inhibition in POMA
These studies demonstrate that in addition to its previously described role as a splicing activator, Nova-1 autoregulates its own expression by acting as a splicing repressor.
Assays of splicing intermediates of Nova (show HNRNPK Proteins)-regulated transcripts in mouse brain revealed that Nova (show HNRNPK Proteins) preferentially regulates removal of introns harbouring (or closest to) YCAY clusters
This gene encodes a neuron-specific RNA-binding protein, a member of the Nova family of paraneoplastic disease antigens, that is recognized and inhibited by paraneoplastic antibodies. These antibodies are found in the sera of patients with paraneoplastic opsoclonus-ataxia, breast cancer, and small cell lung cancer. Alternatively spliced transcripts encoding distinct isoforms have been described.
neuro-oncological ventral antigen 1
, lipid A export ATP-binding/permease protein
, RNA-binding protein Nova-1
, onconeural ventral antigen 1
, paraneoplastic Ri antigen
, ventral neuron-specific protein 1