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NRL encodes a basic motif-leucine zipper transcription factor of the Maf subfamily. Additionally we are shipping NRL Proteins (3) and NRL Kits (1) and many more products for this protein.
Showing 10 out of 18 products:
Human Polyclonal NRL Primary Antibody for ELISA, WB - ABIN1451388
Farjo, Jackson, Pieke-Dahl, Scott, Kimberling, Sieving, Richards, Swaroop: Human bZIP transcription factor gene NRL: structure, genomic sequence, and fine linkage mapping at 14q11.2 and negative mutation analysis in patients with retinal degeneration. in Genomics 1998
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the function of NRL is modulated by its interaction with specific repressor proteins, related to cross-talk between signaling pathways in the retina.
REEP6.1 is a key functional target of NRL (show NRF1 Antibodies)-centered transcriptional regulatory network in rod photoreceptors.
The c.146 C>T mutation in NRL gene causes autosomal dominant retinitis pigmentosa for this family.
In another family a variant, p.M96T in the NRL gene was detected as a retinitis pigmentosa-causing mutation.
This novel p.M96T mutant activated the RHO promoter more intensely than did wild-type NRL in a family with autosomal dominant retinitis pigmentosa.
Studies suggest an important role of sumoylation in fine-tuning the activity of NRL and thereby incorporating yet another layer of control in gene regulatory networks involved in photoreceptor development and homeostasis.
In this study, NR2E3 (show NR2E3 Antibodies) mutations were found to be responsible for approximately 2.9% of overall retinitis pigmentosa (RP) in Chinese patients, NRL was not associated with RP.
The disease caused by NRL mutations found in this study appears to be more severe
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL gene.
the function of NRL is modulated by its interaction with specific repressor proteins, related to cross-talk between signaling pathways in the retina
The NRL Ser50Thr mutation is associated with selective loss of scotopic function before age 20 years. With time, however, the photopic system becomes affected, leading to loss of the photopic visual field and of visual acuity.
both Nrl and Crx (show CRX Antibodies) are required for full transcriptional activity of the PDE6A (show PDE6A Antibodies) gene
CNGA3 (show CNGA3 Antibodies) expression restored cone function in in CNGA3 (show CNGA3 Antibodies)-/-/Nrl-/- mice, an all-cone model of CNGA3 (show CNGA3 Antibodies) achromatopsia.
REEP6.1 is a key functional target of NRL-centered transcriptional regulatory network in rod photoreceptors.
Data indicate that positive feedback between neural retina leucine zipper factor (NRL) and retinoid-related orphan receptor beta (show RORB Antibodies) gene (Rorb (show RORB Antibodies)) genes reinforces the commitment to a rod differentiation fate.
shRNA-mediated knockdown of Crx (show CRX Antibodies) and Nrl resulted in reduced Kcnv2 (show KCNV2 Antibodies) promoter activity and low endogenous Kcnv2 (show KCNV2 Antibodies) mRNA expression in the retina.
This study analyzed the retinal pigment epithelium from Nrl(-/-) mice of various ages for lipofuscin fluorescence and A2E levels.
Findings suggest that elimination of Nrl in adult rods may represent a unique therapy for retinal degeneration.
Our results show that NRL and CRX (show CRX Antibodies) together control the expression of most, if not all, genes involved in rod phototransduction through a cis (show CISH Antibodies)-regulatory module
found that Nrl activated rhodopsin (show RHO Antibodies) and Ppp2r5c (show PPP2CA Antibodies) transcription by recruiting Tip60 (show KAT5 Antibodies) to promote histone H3 (show HIST3H3 Antibodies)/H4 acetylation
Nrl as a direct transcriptional target of RORbeta (show RORB Antibodies) and suggest that combinatorial action of multiple regulatory factors modulates the expression of Nrl in developing and mature retina.
Nrl-deficient retina may serve as a model for elucidating mechanisms of cone homeostasis and degeneration that would be relevant to understanding diseases of the cone-dominant human macula.
This gene encodes a basic motif-leucine zipper transcription factor of the Maf subfamily. The encoded protein is conserved among vertebrates and is a critical intrinsic regulator of photoceptor development and function. Mutations in this gene have been associated with retinitis pigmentosa and retinal degenerative diseases.
neural retina leucine zipper
, bZIP transcription factor L-Maf
, leucine zipper transcription factor
, neural retina-specific leucine zipper protein
, neural retinal-specific leucine zipper