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PARL encodes a mitochondrial integral membrane protein. Additionally we are shipping PARL Antibodies (46) and many more products for this protein.
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Study confirmed that common variants in PARL and PINK1 (show PINK1 Proteins) were associated with leprosy. Furthermore, PARL and PINK1 (show PINK1 Proteins) could physically interact with each other and were involved in the highly connected network formed by reported leprosy susceptibility genes.
PDK2 (show PDK2 Proteins)/PARL senses defects in mitochondrial bioenergetics.
Adipogenic process can be dissected into 3 stages according to the participation of PARL-PINK1 (show PINK1 Proteins)-Parkin (show PARK2 Proteins) system. Findings reveal the sequential adipogenic events directed by PARL-PINK1 (show PINK1 Proteins)-Parkin (show PARK2 Proteins) system, add more evidence supporting the convergence of pathogenesis leading to neurodegenerative and metabolic disease
These findings enrich the allelic spectrum of ABCC5 (show ABCC5 Proteins) in PACG. We identified no tagging SNP responsible for the association of the whole region.
These results reveal a pro-apoptotic function of PARL and identify PARL-mediated Smac (show DIABLO Proteins) processing and cytochrome c (show CYCS Proteins) release facilitated by OPA1 (show OPA1 Proteins)-dependent cristae remodelling as two independent pro-apoptotic pathways in mitochondria.
pathogenic PINK1 (show PINK1 Proteins) mutants which are not cleaved by PARL affect PINK1 (show PINK1 Proteins) kinase activity and the ability to induce PARK2 (show PARK2 Proteins)-mediated mitophagy.
Common genetic variants of the PINK1 (show PINK1 Proteins) and PARL genes are unlikely to be involved in schizophrenia.
the frequency of the haplotype AAC, and AAT were significantly higher in the unaffected cases and the frequencies of haplotype GGT were significantly higher in LHON cases
Rhomboid protease PARL mediates the mitochondrial membrane potential loss-induced cleavage of PGAM5 (show PGAM5 Proteins).
p.S77N variant, and, possibly, mutations in the PARL protein overall, are not a frequent cause of autosomal recessive early-onset Parkinson's disease
Downregulation of PARL after ischemia is a key step in ischemic neuronal injury, and that it decreases HtrA2 (show HTRA2 Proteins) processing and increases neuronal vulnerability.
the OPA1/PARL dependent pathway of cristae remodeling is implicated in heat shock.
Suppression of PARL protein in healthy myotubes lowered mitochondrial mass and insulin (show INS Proteins)-stimulated glycogen (show GYS1 Proteins) synthesis and increased reactive oxygen species production.
results indicate a different function and mechanism of Hax1 (show HAX1 Proteins) in apoptosis and re-opens the question of whether mammalian PARL, in addition to apoptosis, regulates mitochondrial stress response through Omi/HtrA2 (show HTRA2 Proteins) processing.
Parl-/- mitochondria display reduced levels of OPA1, and OPA1 specifically targeted to IMS complements Parl-/- cells, substantiating the importance of PARL in OPA1 processing.(PARL protein, mouse)
Hax1 (show HAX1 Proteins), is required to suppress apoptosis in lymphocytes and neurons; suppression requires the interaction of Hax1 (show HAX1 Proteins) with the mitochondrial proteases Parl and HtrA2 (show HTRA2 Proteins)
This gene encodes a mitochondrial integral membrane protein. Following proteolytic processing of this protein, a small peptide (P-beta) is formed and translocated to the nucleus. This gene may be involved in signal transduction via regulated intramembrane proteolysis of membrane-tethered precursor proteins. Variation in this gene has been associated with increased risk for type 2 diabetes. Alternative splicing results in multiple transcript variants encoding different isoforms.
mitochondrial intramembrane cleaving protease PARL
, mitochondrial intramembrane-cleaving protease PARL
, presenilins-associated rhomboid-like protein, mitochondrial
, rhomboid 7 homolog 1
, presenilin associated, rhomboid-like isoform 1 preproprotein
, presenilin associated, rhomboid-like preproprotein