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European Journal of Pediatrics|January 9, 2007
A newborn with VLCAD deficiency. Clinical, biochemical, and histopathological findingsDidem Aliefendioğlu, Ali Dursun, Turgay Coşkun, et al.European Journal of Biochemistry|December 12, 1997
Transport of activated fatty acids by the peroxisomal ATP-binding-cassette transporter Pxa2 in a semi-intact yeast cell systemN Verleur, E H Hettema, C W van Roermund, et al.Journal of Lipid Research|April 3, 2004
Identification of the peroxisomal beta-oxidation enzymes involved in the degradation of long-chain dicarboxylic acidsSacha Ferdinandusse, Simone Denis, Carlo W T Van Roermund, et al.International Journal of Food Sciences and Nutrition|April 6, 2016
Fat composition of vegetable oil spreads and margarines in the USA in 2013: a national marketplace analysisMarcella Garsetti, Douglas A Balentine, Peter L Zock, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|December 1, 1996
Ischemia-induced transplant arteriosclerosis in the rat. Induction of peptide growth factor expressionJ Waltenberger, M L Akyürek, M Aurivillius, et al.Epigenetics|March 12, 2009
Histone H3 lysine 27 trimethylation in adult differentiated colon associated to cancer DNA hypermethylationAlvaro Rada-Iglesias, Stefan Enroth, Robin Andersson, et al.FEBS Letters|March 9, 1992
Subcellular localisation and processing of non-specific lipid transfer protein are not aberrant in Rhizomelic Chondrodysplasia Punctata fibroblastsJ C Heikoop, B C Ossendorp, R J Wanders, et al.American Journal of Human Genetics|August 12, 1999
PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disordersY Liu, J Björkman, A Urquhart, et al.Nature Communications|January 6, 2026
Persistent river heatwaves are emerging worldwide under climate changeYiling Chen, Zhiying Su, R Iestyn Woolway, et al.European Journal of Pediatrics|October 17, 1998
Stroke-like encephalopathy in an infant with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiencyM Huemer, A Muehl, K Wandl-Vergesslich, et al.Pageof 132