| 000 | 01676 a2200457 4500 | ||
|---|---|---|---|
| 005 | 20250514000703.0 | ||
| 264 | 0 | _c20010906 | |
| 008 | 200109s 0 0 eng d | ||
| 022 | _a0300-5127 | ||
| 024 | 7 |
_a10.1042/0300-5127:0290250 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWanders, R J | |
| 245 | 0 | 0 |
_aPeroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases. _h[electronic resource] |
| 260 |
_bBiochemical Society transactions _cMay 2001 |
||
| 300 |
_a250-67 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Review | ||
| 650 | 0 | 4 |
_aAdenosine Triphosphate _xmetabolism |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aBiological Transport |
| 650 | 0 | 4 |
_aCarbon Dioxide _xmetabolism |
| 650 | 0 | 4 |
_aCarnitine _xmetabolism |
| 650 | 0 | 4 |
_aCarnitine O-Palmitoyltransferase _xmetabolism |
| 650 | 0 | 4 |
_aFatty Acids _xchemistry |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aIntracellular Membranes _xmetabolism |
| 650 | 0 | 4 |
_aMitochondria _xenzymology |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 |
_aPeroxisomal Disorders _xenzymology |
| 650 | 0 | 4 |
_aPeroxisomes _xenzymology |
| 650 | 0 | 4 |
_aRacemases and Epimerases _xdeficiency |
| 650 | 0 | 4 | _aSubstrate Specificity |
| 650 | 0 | 4 |
_aWater _xmetabolism |
| 700 | 1 | _aVreken, P | |
| 700 | 1 | _aFerdinandusse, S | |
| 700 | 1 | _aJansen, G A | |
| 700 | 1 | _aWaterham, H R | |
| 700 | 1 | _avan Roermund, C W | |
| 700 | 1 | _aVan Grunsven, E G | |
| 773 | 0 |
_tBiochemical Society transactions _gvol. 29 _gno. Pt 2 _gp. 250-67 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1042/0300-5127:0290250 _zAvailable from publisher's website |
| 999 |
_c11288398 _d11288398 |
||