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peroxisomal
- Peroxisomal acyl-CoA oxidase deficiency is a disorder that causes deterioration of nervous system functions (neurodegeneration) beginning in infancy. Newborns with ...
- ... gene provides instructions for making a protein called peroxisomal biogenesis factor 7, which is part of a group known as the peroxisomal assembly (PEX) proteins. Within cells, PEX proteins are ...
- ... gene provides instructions for making an enzyme called peroxisomal straight-chain acyl-CoA oxidase. This enzyme is ... enzymes that break down many different substances. The peroxisomal straight-chain acyl-CoA oxidase enzyme plays a ...
- ... third steps, respectively, of a process called the peroxisomal fatty acid beta-oxidation pathway. This process shortens ... D-3-hydroxyacyl-CoA dehydratase D-bifunctional protein, peroxisomal DBP hydroxysteroid (17-beta) dehydrogenase 4 MFE-2 ...
- ... gene provides instructions for making a protein called peroxisomal biogenesis factor 1 (Pex1p), which is part of ... Functional association of the AAA complex and the peroxisomal importomer. FEBS J. 2006 Aug;273(16):3804- ...
- ... homocystinuria. More About This Health Condition 69 kDa peroxisomal ABC-transporter ABC41 ATP-binding cassette sub-family ... D (ALD), member 4 EST352188 MAHCJ P70R P79R peroxisomal membrane protein 69 PMP69 PMP70-related protein PXMP1- ...
- ... dihydroxyacetone phosphate synthase alkyldihydroxyacetone phosphate synthetase alkyldihydroxyacetonephosphate synthase, peroxisomal alkylglycerone-phosphate synthase Tests of AGPS PubMed ALKYLGLYCERONE- ...
- ... dioxygenase phytanoyl-CoA alpha-hydroxylase phytanoyl-CoA dioxygenase, peroxisomal Tests of PHYH PubMed PHYTANOYL-CoA HYDROXYLASE; PHYH ...
- ... Hepatic AGT deficiency Hyperoxaluria, primary Oxalosis Oxaluria, primary Peroxisomal alanine:glyoxylate aminotransferase deficiency Primary oxalosis Primary oxaluria ...
- ... third steps, respectively, of a process called the peroxisomal fatty acid beta-oxidation pathway. This process shortens ... condition. 17-beta-hydroxysteroid dehydrogenase IV deficiency Bifunctional peroxisomal enzyme deficiency DBP deficiency PBFE deficiency Peroxisomal bifunctional ...