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Medical Biology|January 1, 1985
Impaired glycerophosphorylcholine synthesis in murine muscular dystrophyJ P InfanteThe Biochemical Journal|July 1, 1973
Inhibition of phosphatidylcholine synthesis in mammary tissue by 2-chloroethyltrimethylammonium chlorideJ P Infante, J E KinsellaFEBS Letters|February 23, 2000
Secondary carnitine deficiency and impaired docosahexaenoic (22:6n-3) acid synthesis: a common denominator in the pathophysiology of diseases of oxidative phosphorylation and beta-oxidationJ P Infante, V A HuszaghMolecular and Cellular Biochemistry|June 1, 1988
On the nature of the Duchenne muscular dystrophy locus: a portion of a complex of related gene clusters of recent pseudoautosomal origin?J P Infante, V A HuszaghLipids|October 1, 1976
Phospholipid synthesis in mammary tissue. Choline and ethanolamine kinases: kinetic evidence for two discrete active sitesJ P Infante, J E KinsellaFEBS Letters|July 31, 1998
Analysis of the putative role of 24-carbon polyunsaturated fatty acids in the biosynthesis of docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acidsJ P Infante, V A HuszaghMolecular Genetics and Metabolism|February 13, 2001
Zellweger syndrome knockout mouse models challenge putative peroxisomal beta-oxidation involvement in docosahexaenoic acid (22:6n-3) biosynthesisJ P Infante, V A HuszaghMolecular Genetics and Metabolism|March 13, 2001
Impaired arachidonic (20:4n-6) and docosahexaenoic (22:6n-3) acid synthesis by phenylalanine metabolites as etiological factors in the neuropathology of phenylketonuriaJ P Infante, V A HuszaghMolecular and Cellular Biochemistry|July 8, 1999
Mechanisms of resistance to pathogenesis in muscular dystrophiesJ P Infante, V A HuszaghMolecular and Cellular Biochemistry|March 1, 1997
On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disordersJ P Infante, V A HuszaghPageof 3