Publications
Found 15 results
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“Attenuated mRNA expression of lipid metabolism genes in primary hepatocytes following lipopolysaccharide treatment in dairy cows”, vol. 14, pp. 3718-3728, 2015.
, “Cloning and prokaryotic expression of the porcine lipasin gene”, vol. 14, pp. 14698-14705, 2015.
, “Molecular cloning and tissue distribution profiles of the chicken R-spondin1 gene”, vol. 14, pp. 3090-3097, 2015.
, “Expression of the porcine lipoic acid synthase (LIAS) gene in Escherichia coli”, vol. 13, pp. 5369-5377, 2014.
, “Lactoferrin mRNA expression in mouse mammary glands during pregnancy and lactation”, vol. 13, pp. 4747-4755, 2014.
, “Protection against Taenia pisiformis larval infection induced by a recombinant oncosphere antigen vaccine”, vol. 13, pp. 6148-6159, 2014.
, “Isolation and identification of bovine primary hepatocytes”, vol. 12, pp. 5186-5194, 2013.
, “Molecular cloning and expression of the porcine S14R gene in Escherichia coli”, vol. 12, pp. 4405-4412, 2013.
, “Synonymous codon usage patterns in different parasitic platyhelminth mitochondrial genomes”, vol. 12, pp. 587-596, 2013.
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http://dx.doi.org/10.1006/geno.2001.6531
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http://dx.doi.org/10.1111/j.1550-7408.2011.00613.x
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Jia W and Higgs PG (2008). Codon usage in mitochondrial genomes: distinguishing context-dependent mutation from translational selection. Mol. Biol. Evol. 25: 339-351.
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Liu Q, Feng Y and Xue Q (2004). Analysis of factors shaping codon usage in the mitochondrion genome of Oryza sativa. Mitochondrion 4: 313-320.
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Luo XL, Xu JG and Ye CY (2011). Analysis of synonymous codon usage in Shigella flexneri 2a strain 301 and other Shigella and Escherichia coli strains. Can. J. Microbiol. 57: 1016-1023.
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Whittle CA, Sun Y and Johannesson H (2011). Evolution of synonymous codon usage in Neurospora tetrasperma and Neurospora discreta. Genome Biol. Evol. 3: 332-343.
http://dx.doi.org/10.1093/gbe/evr018
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Zhou M and Li X (2009). Analysis of synonymous codon usage patterns in different plant mitochondrial genomes. Mol. Biol. Rep. 36: 2039-2046.
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“Conjugated linoleic acid-induced milk fat reduction associated with depressed expression of lipogenic genes in lactating Holstein mammary glands”, vol. 11, pp. 4754-4764, 2012.
, Barber MC, Vallance AJ, Kennedy HT and Travers MT (2003). Induction of transcripts derived from promoter III of the acetyl-CoA carboxylase-alpha gene in mammary gland is associated with recruitment of SREBP-1 to a region of the proximal promoter defined by a DNase I hypersensitive site. Biochem. J. 375: 489-501.
http://dx.doi.org/10.1042/BJ20030480
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Bauman DE and Griinari JM (2003). Nutritional regulation of milk fat synthesis. Annu. Rev. Nutr. 23: 203-227.
http://dx.doi.org/10.1146/annurev.nutr.23.011702.073408
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Bauman DE, Perfield JW, Harvatine KJ and Baumgard LH (2008). Regulation of fat synthesis by conjugated linoleic acid: lactation and the ruminant model. J. Nutr. 138: 403-409. Baumgard LH, Corl BA, Dwyer DA, Saebo A, et al. (2000). Identification of the conjugated linoleic acid isomer that inhibits milk fat synthesis. Am. J. Physiol. Regul. Integr. Comp Physiol. 278: R179-R184.
Baumgard LH, Sangster JK and Bauman DE (2001). Milk fat synthesis in dairy cows is progressively reduced by increasing supplemental amounts of trans-10, cis-12 conjugated linoleic acid (CLA). J. Nutr. 131: 1764-1769.
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Baumgard LH, Matitashvili E, Corl BA, Dwyer DA, et al. (2002). trans-10, cis-12 conjugated linoleic acid decreases lipogenic rates and expression of genes involved in milk lipid synthesis in dairy cows. J. Dairy Sci. 85: 2155-2163.
http://dx.doi.org/10.3168/jds.S0022-0302(02)74294-X
Belury MA (2002). Dietary conjugated linoleic acid in health: physiological effects and mechanisms of action. Annu. Rev. Nutr. 22: 505-531.
http://dx.doi.org/10.1146/annurev.nutr.22.021302.121842
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Bernard L, Leroux C and Chilliard Y (2008). Expression and nutritional regulation of lipogenic genes in the ruminant lactating mammary gland. Adv. Exp. Med. Biol. 606: 67-108.
http://dx.doi.org/10.1007/978-0-387-74087-4_2
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Bionaz M and Loor JJ (2008). Gene networks driving bovine milk fat synthesis during the lactation cycle. BMC. Genomics 9: 366.
http://dx.doi.org/10.1186/1471-2164-9-366
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Chouinard PY, Corneau L, Barbano DM, Metzger LE, et al. (1999). Conjugated linoleic acids alter milk fatty acid composition and inhibit milk fat secretion in dairy cows. J Nutr. 129: 1579-1584.
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Gervais R, McFadden JW, Lengi AJ, Corl BA, et al. (2009). Effects of intravenous infusion of trans-10, cis-12 18:2 on mammary lipid metabolism in lactating dairy cows. J. Dairy Sci. 92: 5167-5177.
http://dx.doi.org/10.3168/jds.2009-2281
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Giesy JG, McGuire MA, Shafii B and Hanson TW (2002). Effect of dose of calcium salts of conjugated linoleic acid (CLA) on percentage and fatty acid content of milk fat in midlactation holstein cows. J. Dairy Sci. 85: 2023-2029.
http://dx.doi.org/10.3168/jds.S0022-0302(02)74279-3
Griinari JM, Corl BA, Lacy SH, Chouinard PY, et al. (2000). Conjugated linoleic acid is synthesized endogenously in lactating dairy cows by Delta(9)-desaturase. J. Nutr. 130: 2285-2291.
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Harvatine KJ and Bauman DE (2006). SREBP1 and thyroid hormone responsive spot 14 (S14) are involved in the regulation of bovine mammary lipid synthesis during diet-induced milk fat depression and treatment with CLA. J. Nutr. 136: 2468-2474.
PMid:16988111
Huang Y, Schoonmaker JP, Bradford BJ and Beitz DC (2008). Response of milk fatty acid composition to dietary supplementation of soy oil, conjugated linoleic acid, or both. J. Dairy Sci. 91: 260-270.
http://dx.doi.org/10.3168/jds.2007-0344
PMid:18096948
Kadegowda AK, Bionaz M, Thering B, Piperova LS, et al. (2009). Identification of internal control genes for quantitative polymerase chain reaction in mammary tissue of lactating cows receiving lipid supplements. J. Dairy Sci. 92: 2007-2019.
http://dx.doi.org/10.3168/jds.2008-1655
PMid:19389958
Kadegowda AK, Connor EE, Teter BB, Sampugna J, et al. (2010). Dietary trans fatty acid isomers differ in their effects on mammary lipid metabolism as well as lipogenic gene expression in lactating mice. J. Nutr. 140: 919-924.
http://dx.doi.org/10.3945/jn.109.110890
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Khan SA and Vanden Heuvel JP (2003). Role of nuclear receptors in the regulation of gene expression by dietary fatty acids (review). J. Nutr. Biochem. 14: 554-567.
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Lock AL, Teles BM, Perfield JW, Bauman DE, et al. (2006). A conjugated linoleic acid supplement containing trans-10, cis-12 reduces milk fat synthesis in lactating sheep. J. Dairy Sci. 89: 1525-1532.
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Loor JJ, Ferlay A, Ollier A, Doreau M, et al. (2005). Relationship among trans and conjugated fatty acids and bovine milk fat yield due to dietary concentrate and linseed oil. J. Dairy Sci. 88: 726-740.
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Perfield JW, Bernal-Santos G, Overton TR and Bauman DE (2002). Effects of dietary supplementation of rumen-protected conjugated linoleic acid in dairy cows during established lactation. J. Dairy Sci. 85: 2609-2617.
http://dx.doi.org/10.3168/jds.S0022-0302(02)74346-4
Peterson DG, Baumgard LH and Bauman DE (2002). Milk fat response to low doses of trans-10, cis-12 conjugated linoleic acid(CLA). J. Dairy Sci. 85: 1764-1766.
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Peterson DG, Matitashvili EA and Bauman DE (2004). The inhibitory effect of trans-10, cis-12 CLA on lipid synthesis in bovine mammary epithelial cells involves reduced proteolytic activation of the transcription factor SREBP-1. J. Nutr. 134: 2523-2527.
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Viswanadha S, Giesy JG, Hanson TW and McGuire MA (2003). Dose response of milk fat to intravenous administration of the trans-10, cis-12 isomer of conjugated linoleic acid. J. Dairy Sci. 86: 3229-3236.
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“Leptin mRNA expression in the rat mammary gland at different activation stages”, vol. 10, pp. 3657-3663, 2011.
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