Examples of 'peroxisomal' in a sentence
Meaning of "peroxisomal"
peroxisomal (adjective) - 'Peroxisomal' is a term used in biology to refer to structures or functions associated with peroxisomes, which are cell organelles involved in processes such as lipid metabolism and the detoxification of harmful substances
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- Of or pertaining to the peroxisome
How to use "peroxisomal" in a sentence
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peroxisomal
All peroxisomal proteins are encoded by nuclear genes.
Definite diagnosis requires evaluation of peroxisomal functions.
Treatment of peroxisomal and lysosomal diseases.
Import of proteins into the peroxisomal matrix.
His research on peroxisomal disorders achieved international recognition.
Transamination of glyoxylate to glycine is also catalysed by a peroxisomal enzyme.
The function of this peroxisomal membrane protein is unknown.
There is also a marked species difference for peroxisomal effects.
Eleven separate peroxisomal disorders have now been identified.
The protein encoded by this gene is an integral peroxisomal membrane protein.
Peroxisomal defect is likely to affect phagocytosis and antigen presentation capacity of microglia.
The protein is thought to be involved in peroxisomal matrix protein import.
All peroxisomal proteins are synthesized in the cytoplasm and must be directed to the peroxisome.
The model allows for mitochondrial and peroxisomal compartmentalization.
These aspects of peroxisomal protein import resemble protein tranport into the nucleus.
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The model allowed for mitochondrial and peroxisomal compartmentalization.
Altering peroxisomal but not mitochondrial FAO promotes early differentiation of satellite cells.
Cytosolic expression may be achieved by deletion or modification of a mitochondrial or peroxisomal targeting signal.
Mutations of the gene are a cause of peroxisomal disorders such as Zellweger syndrome.
Aox oligomers are formed only after the import into the peroxisomal matrix.
Other peroxisomal proteins contain a signal sequence near the N terminus.
Sequence analysis of this clone confirmed it to be the yeast peroxisomal catalase gene.
PCILux expresses peroxisomal luciferase under control of the hCMV IE promoter.
EH is considered to be the proximate peroxisomal proliferator.
Two peroxisomal targeting signals have been identified,.
It was found that PEP carboxykinase derived from Actinobacillus succinogenes comprises a peroxisomal targeting signal.
In this thesis I will look into peroxisomal dynamics in the intestinal crypt.
Peroxisomal protein transport is defective in the following genetic diseases,.
Interestingly, butyrate was not a significant peroxisomal proliferation activator.
Accordingly, peroxisomal defects often lead to impairment of ether-lipid production.
X-linked adrenoleukodystrophy is the most common peroxisomal disorder.
Furthermore, no hepatic peroxisomal proliferation can be detected histochemically.
This compound is synthesized by microbial biotransformation on the peroxisomal ¿ - oxidation pathway.
Peroxisomal oxidation is induced by a high-fat diet and administration of hypolipidemic drugs like clofibrate.
In liver, pristanic acid is degraded by peroxisomal beta oxidation to propionyl-CoA.
Peroxisomal beta-oxidation showed equivalent activity with palmitoyl CoA or n-octanoyl CoA as substrate.
In glyoxysomes the fatty acids are hydrolyzed to acetyl-CoA by peroxisomal β-oxidation enzymes.
The extension contains a peroxisomal targeting signal, so that LDHBx is imported into the peroxisome.
Thiazolidinediones are selective agonists for the nuclear receptor peroxisomal proliferator-activated receptor gamma.
The group 1 peroxisomal disorders are characterized by a virtually complete loss of peroxisomes and peroxisomal functions.
Evidence suggests that PPARδ controls the peroxisomal beta-oxidation pathway of fatty acids.
Peroxisomal β-oxidation also requires enzymes specific to the peroxisome and to very long fatty acids.
There are three key differences between the enzymes used for mitochondrial and peroxisomal β-oxidation,.
Other peroxisomal proteins contain a signal at the N-terminus.
The salt resistance of additional PNC1 maybe the result of a peroxisomal function of Pnc1.
Peroxisomal protein transport is defective in the following genetic diseases, Zellweger syndrome.
The Zellweger cerebro-hepato-renal syndrome represents the most serious peroxisomal disease.
Bi-functional protein D is a peroxisomal enzyme involved in the beta-oxidation of very long fatty acids.
The phaC transgene is linked in frame with a suitable N-terminal or C-terminal peroxisomal targeting sequence.
Remove peroxisomal targeting sequence The translocation signal at the C-terminus of the luciferases was removed.