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Showing results (31-40 of 35) with videos related to

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Advances in Experimental Medicine and Biology|March 10, 2000
Characterization of a response element for peroxisomal proliferator activated receptor (PPRE) in human muscle-type carnitine palmitoyltransferase IC Mascaró, E Acosta, J A Ortiz, et al.
Cahiers D'Anesthesiologie|May 1, 1986
[Dobutamine in vascular surgery]R Muchada, B Lavandier, S Estanove, et al.
The Biochemical Journal|January 12, 1999
Isolation of pig mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase gene promoter: characterization of a peroxisome proliferator-responsive elementJ A Ortiz, J Mallolas, C Nicot, et al.
Journal of Lipid Research|November 1, 1996
Aberrantly spliced mRNAs of the 3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) gene with a donor splice-site point mutation produce hereditary HL deficiencyC Buesa, J Pié, A Barceló, et al.
The Biochemical Journal|April 15, 1997
A nonsense mutation in the 3-hydroxy-3-methylglutaryl-CoA lyase gene produces exon skipping in two patients of different origin with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyJ Pié, N Casals, C H Casale, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Advances in Experimental Medicine and Biology|March 10, 2000
Characterization of a response element for peroxisomal proliferator activated receptor (PPRE) in human muscle-type carnitine palmitoyltransferase IC Mascaró, E Acosta, J A Ortiz, et al.
Cahiers D'Anesthesiologie|May 1, 1986
[Dobutamine in vascular surgery]R Muchada, B Lavandier, S Estanove, et al.
The Biochemical Journal|January 12, 1999
Isolation of pig mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase gene promoter: characterization of a peroxisome proliferator-responsive elementJ A Ortiz, J Mallolas, C Nicot, et al.
Journal of Lipid Research|November 1, 1996
Aberrantly spliced mRNAs of the 3-hydroxy-3-methylglutaryl coenzyme A lyase (HL) gene with a donor splice-site point mutation produce hereditary HL deficiencyC Buesa, J Pié, A Barceló, et al.
The Biochemical Journal|April 15, 1997
A nonsense mutation in the 3-hydroxy-3-methylglutaryl-CoA lyase gene produces exon skipping in two patients of different origin with 3-hydroxy-3-methylglutaryl-CoA lyase deficiencyJ Pié, N Casals, C H Casale, et al.
Pageof 4