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

Author： 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  

Publisher： Oxford University Press

ISSN： 1460-2083

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

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Metabolic Engineering of Plants to Produce Very Long-chain Polyunsaturated Fatty Acids

By Truksa Martin   Wu Guohai   Vrinten Patricia   Qiu Xiao  

Transgenic Research, Vol. 15, Iss. 2, 2006-04 ,pp. : 131-137

Springer Publishing Company

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite