Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency

By Oezen Iris  

Human Molecular Genetics, Vol. 14, Iss. 9, 2005-05 ,pp. : 1127-1137

Oxford University Press

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Loss of functional ELOVL4 depletes very long-chain fatty acids (≥C28) and the unique -O-acylceramides in skin leading to neonatal death

By Vasireddy Vidyullatha   Uchida Yoshikazu   Kim Soo Yeon   Mandal Md Nawajesh Ali   Reddy Geereddy Bhanuprakash   Bodepudi Ravi   Alderson Nathan L.   Brown Johnie C.   Hama Hiroko   Dlugosz Andrzej   Elias Peter M.   Holleran Walter M.   Ayyagari Radha  

Human Molecular Genetics, Vol. 16, Iss. 5, 2007-03 ,pp. : 471-482

Oxford University Press

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Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse

By Rhead W.J.  

Human Molecular Genetics, Vol. 10, Iss. 19, 2001-09 ,pp. : 2069-2077

Oxford University Press

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Drosophila models of peroxisomal biogenesis disorder: peroxins are required for spermatogenesis and very-long-chain fatty acid metabolism

By Chen Haiyang   Liu Zhonghua   Huang Xun  

Human Molecular Genetics, Vol. 19, Iss. 3, 2010-02 ,pp. : 494-505

Oxford University Press

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A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy

By Heinzer Ann K.  

Human Molecular Genetics, Vol. 12, Iss. 10, 2003-05 ,pp. : 1145-1154

Oxford University Press

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