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CNBP encodes a nucleic-acid binding protein with seven zinc-finger domains. Zusätzlich bieten wir Ihnen CNBP Proteine (15) und CNBP Kits (1) und viele weitere Produktgruppen zu diesem Protein an.
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Human Polyclonal CNBP Primary Antibody für WB - ABIN1881216
Panayiotopoulos, Scarpalezos: Dystrophia myotonica. Peripheral nerve involvement and pathogenetic implications. in Journal of the neurological sciences 1976
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Human Polyclonal CNBP Primary Antibody für ELISA, WB - ABIN269994
Day, Ricker, Jacobsen, Rasmussen, Dick, Kress, Schneider, Koch, Beilman, Harrison, Dalton, Ranum: Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum. in Neurology 2003
A G-rich motif in the lncRNA Braveheart interacts with Cnbp to specify the cardiovascular lineage.
The cnbp overexpression rescued the Treacher Collins Syndrome phenotype in a dose-dependent manner by a reactive oxygen species-cytoprotective action that prevented the redox-responsive genes' upregulation but did not normalize the synthesis of ribosomal RNAs.
High CNBP expression is associated with Medulloblastoma.
CNBP overexpression caused increase of cell death and suppression of cell metastasis through its induction of G-quadruplex formation in the promoter of hnRNP K (zeige HNRNPK Antikörper) resulting in hnRNP K (zeige HNRNPK Antikörper) down-regulation
Arginine methylation of CNBP in the RG motif does not change the subcellular localization but regulates its RNA binding activity.
CNBP are novel antigens for SLE patients and the recognition of CNBP might be differentiated dependent on the level of arginine methylation.
suggested a new possibility of CNBP as a potential anti-cancer target based on CNBP's biological function in c-myc (zeige MYC Antikörper) transcription
CNBP associates with the poly(A) binding protein and accumulates in stress granules.
The co-segregation of Myotonic dystrophy type 2 with a recessive CLCN1 (zeige CLCN1 Antikörper) mutation provided the explanation for the unusual clinical findings for juvenile onset of myotonia in a 14-year-old female with Myotonic dystrophy type 2 and her affected mother
Myotonic dystrophy 2(autosomal dominant, multisystem disorder caused by a CCTG (zeige CCT3 Antikörper) tetranucleotide repeat expansion located in intron 1 of the zinc finger protein 9 gene (ZNF9 gene) on chromosome 3q 21.3.) described in Israeli Jewish European ancestry.
data support a role for CNBP as a critical transcription factor and a key regulator of the prolonged expression of sustained cytokine IL-6 (zeige IL6 Antikörper) during persistent LPS (zeige TLR4 Antikörper) stimulation or Gram-negative bacterial infection
CNBP up-regulates tbx2b and smarca5 (zeige SMARCA5 Antikörper), and down-regulates wnt5b (zeige WNT5B Antikörper) gene expression.
expression of APP (zeige APP Antikörper)(Swe) in murine tissue induces a decrease in CNBP expression.
CNBP targets Myc (zeige MYC Antikörper) in rostral head formation, is essential for forebrain induction and specification.
This gene encodes a nucleic-acid binding protein with seven zinc-finger domains. The protein has a preference for binding single stranded DNA and RNA. The protein functions in cap-independent translation of ornithine decarboxylase mRNA, and may also function in sterol-mediated transcriptional regulation. A CCTG expansion in the first intron of this gene results in myotonic dystrophy type 2. Multiple transcript variants encoding different isoforms have been found for this gene.
cellular nucleic acid-binding protein
, zinc finger protein 9
, cellular nucleic acid binding protein
, erythroid differentiation-related
, sterol regulatory element-binding protein
, zinc finger protein 273
, zinc finger protein 9 (a cellular retroviral nucleic acid binding protein)
, cellular nucleic acid binding protein 1
, cellular nucleic acid binding protein a
, DNA binding protein