The absence of ABCD2 sensitizes mice to disruptions in lipid metabolism by dietary erucic acid[S]
暂无分享,去创建一个
Xiang-An Li | A. Morris | G. Graf | Manjula Sunkara | A. Pujol | J. A. Brown | Saloni Bhatnagar | Shuang Liang | Jing-jing Liu | Xiaoxi Liu | Kylie E Newman | J. A. Brown
[1] S. Stamm,et al. C6 pyridinium ceramide influences alternative pre-mRNA splicing by inhibiting protein phosphatase-1 , 2011, Nucleic acids research.
[2] S. Nakashima,et al. Induction of peroxisomal lipid metabolism in mice fed a high-fat diet. , 2011, Molecular medicine reports.
[3] H. Waterham,et al. Differential substrate specificities of human ABCD1 and ABCD2 in peroxisomal fatty acid β-oxidation. , 2011, Biochimica et biophysica acta.
[4] H. Ren,et al. A Phosphatidic Acid Binding/Nuclear Localization Motif Determines Lipin1 Function in Lipid Metabolism and Adipogenesis , 2010, Molecular biology of the cell.
[5] Matej Oresic,et al. Peroxisomal and Microsomal Lipid Pathways Associated with Resistance to Hepatic Steatosis and Reduced Pro-inflammatory State* , 2010, The Journal of Biological Chemistry.
[6] Xiang-An Li,et al. ABCD2 is abundant in adipose tissue and opposes the accumulation of dietary erucic acid (C22:1) in fat[S] , 2010, Journal of Lipid Research.
[7] I. Ferrer,et al. General Aspects and Neuropathology of X‐Linked Adrenoleukodystrophy , 2009, Brain pathology.
[8] R. Coleman,et al. Hepatic triacylglycerol accumulation and insulin resistance This work was supported by National Institutes of Health Grants DK56598, DK59935, and DK56350. Published, JLR Papers in Press, November 6, 2008. , 2009, Journal of Lipid Research.
[9] H. Waterham,et al. The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl–CoA esters , 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[10] Eric J. Rouse,et al. Defects in the Leptin Axis Reduce Abundance of the ABCG5-ABCG8 Sterol Transporter in Liver* , 2007, Journal of Biological Chemistry.
[11] H. Waterham,et al. The peroxisomal ABC transporter family , 2007, Pflügers Archiv - European Journal of Physiology.
[12] Ronald J A Wanders,et al. Biochemistry of mammalian peroxisomes revisited. , 2006, Annual review of biochemistry.
[13] A. Bookout,et al. Liver X receptor alpha interferes with SREBP1c-mediated Abcd2 expression. Novel cross-talk in gene regulation. , 2005, The Journal of biological chemistry.
[14] P. Vreken,et al. Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage. , 2005, Human molecular genetics.
[15] R. Wanders,et al. Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouse. , 2005, The Biochemical journal.
[16] J. Mandel,et al. Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy. , 2004, Human molecular genetics.
[17] T. M. Lewin,et al. Do long-chain acyl-CoA synthetases regulate fatty acid entry into synthetic versus degradative pathways? , 2002, The Journal of nutrition.
[18] H. Moser,et al. Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesis. , 2001, The Journal of biological chemistry.
[19] H. Sprecher. Metabolism of highly unsaturated n-3 and n-6 fatty acids. , 2000, Biochimica et biophysica acta.
[20] A. Das,et al. Induction of the Peroxisomal Glycerolipid-synthesizing Enzymes during Differentiation of 3T3-L1 Adipocytes , 2000, The Journal of Biological Chemistry.
[21] A. Holzinger,et al. The four murine peroxisomal ABC-transporter genes differ in constitutive, inducible and developmental expression. , 1999, European journal of biochemistry.
[22] A. Holzinger,et al. cDNA cloning and mRNA expression of the human adrenoleukodystrophy related protein (ALDRP), a peroxisomal ABC transporter. , 1997, Biochemical and biophysical research communications.
[23] J. Mandel,et al. A close relative of the adrenoleukodystrophy (ALD) gene codes for a peroxisomal protein with a specific expression pattern. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[24] S. Tsuji,et al. Physiological significance of fatty acid elongation system in adrenoleukodystrophy , 1991, Journal of the Neurological Sciences.
[25] M. Garg,et al. Dietary cholesterol and/or n-3 fatty acid modulate delta 9-desaturase activity in rat liver microsomes. , 1988, Biochimica et biophysica acta.
[26] M. Garg,et al. Effect of dietary cholesterol and/or omega 3 fatty acids on lipid composition and delta 5-desaturase activity of rat liver microsomes. , 1988, The Journal of nutrition.
[27] B. Christophersen,et al. Metabolism of erucic acid in adipocytes isolated from rat epididymal fat , 1983, Lipids.
[28] J. Bremer,et al. Metabolism of very long-chain monounsaturated fatty acids (22:1) and the adaptation to their presence in the diet. , 1982, Journal of lipid research.
[29] Stéphane Fourcade,et al. A key role for the peroxisomal ABCD2 transporter in fatty acid homeostasis. , 2009, American journal of physiology. Endocrinology and metabolism.
[30] Olga Ilkayeva,et al. Mitochondrial overload and incomplete fatty acid oxidation contribute to skeletal muscle insulin resistance. , 2008, Cell metabolism.
[31] A. Abdellatif,et al. Pathological effects of dietary rapeseed oil in rats. , 1970, Nutrition and metabolism.