- peroxisomal function
- пероксисомная функция
English-Russian small dictionary of medicine. Г.Ю. Бельман, А.Е. Бойков.. 2015.
peroxisomal function
Смотреть что такое "peroxisomal function" в других словарях:
Inborn error of metabolism — Classification and external resources ICD 10 E70 E90 ICD 9 … Wikipedia
Disease — Illness or sickness often characterized by typical patient problems (symptoms) and physical findings (signs). Disruption sequence: The events that occur when a fetus that is developing normally is subjected to a destructive agent such as the… … Medical dictionary
PEX5 — Peroxisomal biogenesis factor 5, also known as PEX5, is a human gene. [cite web | title = Entrez Gene: PEX5 Peroxisomal biogenesis factor 5| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5830| accessdate … Wikipedia
PEX12 — Peroxisomal biogenesis factor 12, also known as PEX12, is a human gene.cite web | title = Entrez Gene: PEX12 peroxisomal biogenesis factor 12| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5193| accessdate … Wikipedia
PXMP3 — Peroxisomal membrane protein 3, also known as PXMP3, is a human gene.cite web | title = Entrez Gene: PXMP3 peroxisomal membrane protein 3, 35kDa (Zellweger syndrome)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia
PEX3 — Peroxisomal biogenesis factor 3, also known as PEX3, is a human gene.cite web | title = Entrez Gene: PEX3 peroxisomal biogenesis factor 3| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=8504| accessdate = ] … Wikipedia
PECR — Peroxisomal trans 2 enoyl CoA reductase PDB rendering based on 1yxm … Wikipedia
Peroxisome — Peroxisomes are ubiquitous organelles in eukaryotes that participate in the metabolism of fatty acids and other metabolites. Peroxisomes have enzymes that rid the cell of toxic peroxides. They have a single lipid bilayer membrane that separates… … Wikipedia
D-bifunctional protein deficiency — Classification and external resources ICD 10 E80.3 OMIM 261515 DiseasesDB … Wikipedia
D-Bifunctional Protein Deficiency — (officially called 17 β hydroxysteroid dehydrogenase) is an autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific… … Wikipedia
ABCD2 — ATP binding cassette, sub family D (ALD), member 2, also known as ABCD2, is a human gene.cite web | title = Entrez Gene: ABCD2 ATP binding cassette, sub family D (ALD), member 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
