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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 I
C 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 element
J 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 deficiency
C 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 deficiency
J Pié, N Casals, C H Casale, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 35) with videos related to
Sort By:
Page
of 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 I
C 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 element
J 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 deficiency
C 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 deficiency
J Pié, N Casals, C H Casale, et al.
Page
of 4