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U B Jensen

Showing results (11-20 of 26) with videos related to

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The American Journal of Physiology|August 1, 1997
Downregulation of aquaporin-2 parallels changes in renal water excretion in unilateral ureteral obstructionJ Frøkiaer, B M Christensen, D Marples, et al.
Biochimica Et Biophysica Acta|October 13, 1992
Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cellsT G Jensen, B S Andresen, P Bross, et al.
Biochemical and Biophysical Research Communications|October 12, 2000
Immunolocalization of AQP9 in liver, epididymis, testis, spleen, and brainM Elkjaer, Z Vajda, L N Nejsum, et al.
The Journal of Investigative Dermatology|September 1, 1994
Gene transfer into cultured human epidermis and its transplantation onto immunodeficient mice: an experimental model for somatic gene therapyU B Jensen, T G Jensen, P K Jensen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 16, 2001
Tail-vein injection of mannan-binding lectin DNA leads to high expression levels of multimeric protein in liverT Vorup-Jensen, U B Jensen, H Liu, et al.
The Journal of Biological Chemistry|May 28, 1998
Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondriaT J Corydon, P Bross, T G Jensen, et al.
American Journal of Human Genetics|September 1, 1993
A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD)B S Andresen, P Bross, T G Jensen, et al.
Human Mutation|January 1, 1995
Comparison between medium-chain acyl-CoA dehydrogenase mutant proteins overexpressed in bacterial and mammalian cellsT G Jensen, P Bross, B S Andresen, et al.
Clinical Genetics|November 18, 2015
JP-HHT phenotype in Danish patients with SMAD4 mutationsA M Jelsig, P M Tørring, A D Kjeldsen, et al.
The Journal of Investigative Dermatology|May 12, 2001
Modulation of keratinocyte gene expression and differentiation by PPAR-selective ligands and tetradecylthioacetic acidM Westergaard, J Henningsen, M L Svendsen, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
The American Journal of Physiology|August 1, 1997
Downregulation of aquaporin-2 parallels changes in renal water excretion in unilateral ureteral obstructionJ Frøkiaer, B M Christensen, D Marples, et al.
Biochimica Et Biophysica Acta|October 13, 1992
Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cellsT G Jensen, B S Andresen, P Bross, et al.
Biochemical and Biophysical Research Communications|October 12, 2000
Immunolocalization of AQP9 in liver, epididymis, testis, spleen, and brainM Elkjaer, Z Vajda, L N Nejsum, et al.
The Journal of Investigative Dermatology|September 1, 1994
Gene transfer into cultured human epidermis and its transplantation onto immunodeficient mice: an experimental model for somatic gene therapyU B Jensen, T G Jensen, P K Jensen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 16, 2001
Tail-vein injection of mannan-binding lectin DNA leads to high expression levels of multimeric protein in liverT Vorup-Jensen, U B Jensen, H Liu, et al.
The Journal of Biological Chemistry|May 28, 1998
Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondriaT J Corydon, P Bross, T G Jensen, et al.
American Journal of Human Genetics|September 1, 1993
A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD)B S Andresen, P Bross, T G Jensen, et al.
Human Mutation|January 1, 1995
Comparison between medium-chain acyl-CoA dehydrogenase mutant proteins overexpressed in bacterial and mammalian cellsT G Jensen, P Bross, B S Andresen, et al.
Clinical Genetics|November 18, 2015
JP-HHT phenotype in Danish patients with SMAD4 mutationsA M Jelsig, P M Tørring, A D Kjeldsen, et al.
The Journal of Investigative Dermatology|May 12, 2001
Modulation of keratinocyte gene expression and differentiation by PPAR-selective ligands and tetradecylthioacetic acidM Westergaard, J Henningsen, M L Svendsen, et al.
Pageof 3