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Human Gene Therapy
|
January 26, 2000
Phenotypic correction of feline lipoprotein lipase deficiency by adenoviral gene transfer
G Liu, K J Ashbourne Excoffon, J E Wilson, et al.
Genomics
|
January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34
S Hadano, K Nichol, R R Brinkman, et al.
Cell Cycle (Georgetown, Tex.)
|
December 25, 2007
N-terminal proteolysis of full-length mutant huntingtin in an inducible PC12 cell model of Huntington's disease
Tamara Ratovitski, Masayuki Nakamura, James D'Ambola, et al.
Journal of Lipid Research
|
June 1, 1994
High frequency of mutations in the human lipoprotein lipase gene in pregnancy-induced chylomicronemia: possible association with apolipoprotein E2 isoform
Y Ma, T C Ooi, M S Liu, et al.
Journal of Lipid Research
|
January 20, 2007
Physiologically regulated transgenic ABCA1 does not reduce amyloid burden or amyloid-beta peptide levels in vivo
Veronica Hirsch-Reinshagen, Jennifer Y Chan, Anna Wilkinson, et al.
Endocrinology
|
April 10, 2014
Prevention of obesity-induced renal injury in male mice by DPP4 inhibition
Ravi Nistala, Javad Habibi, Guido Lastra, et al.
Obesity (Silver Spring, Md.)
|
July 5, 2014
DPP4 inhibition attenuates filtration barrier injury and oxidant stress in the zucker obese rat
Ravi Nistala, Javad Habibi, Annayya Aroor, et al.
Journal of Lipid Research
|
March 18, 2004
The ATP-binding cassette transporter 1 mediates lipid efflux from Sertoli cells and influences male fertility
David M Selva, Veronica Hirsch-Reinshagen, Braydon Burgess, et al.
Experimental Neurology
|
September 1, 2005
Ethyl-EPA treatment improves motor dysfunction, but not neurodegeneration in the YAC128 mouse model of Huntington disease
Jeremy M Van Raamsdonk, Jacqueline Pearson, Daniel A Rogers, et al.
Disease-A-Month : DM
|
May 1, 1995
Recognition, assessment, and treatment of anxiety in the critical care patient
R C Bone, W R Hayden, R L Levine, et al.
Page
of 104
Search research articles
Search
Showing results (691-700 of 1,032) with videos related to
Sort By:
Page
of 104
Human Gene Therapy
|
January 26, 2000
Phenotypic correction of feline lipoprotein lipase deficiency by adenoviral gene transfer
G Liu, K J Ashbourne Excoffon, J E Wilson, et al.
Genomics
|
January 16, 1999
A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34
S Hadano, K Nichol, R R Brinkman, et al.
Cell Cycle (Georgetown, Tex.)
|
December 25, 2007
N-terminal proteolysis of full-length mutant huntingtin in an inducible PC12 cell model of Huntington's disease
Tamara Ratovitski, Masayuki Nakamura, James D'Ambola, et al.
Journal of Lipid Research
|
June 1, 1994
High frequency of mutations in the human lipoprotein lipase gene in pregnancy-induced chylomicronemia: possible association with apolipoprotein E2 isoform
Y Ma, T C Ooi, M S Liu, et al.
Journal of Lipid Research
|
January 20, 2007
Physiologically regulated transgenic ABCA1 does not reduce amyloid burden or amyloid-beta peptide levels in vivo
Veronica Hirsch-Reinshagen, Jennifer Y Chan, Anna Wilkinson, et al.
Endocrinology
|
April 10, 2014
Prevention of obesity-induced renal injury in male mice by DPP4 inhibition
Ravi Nistala, Javad Habibi, Guido Lastra, et al.
Obesity (Silver Spring, Md.)
|
July 5, 2014
DPP4 inhibition attenuates filtration barrier injury and oxidant stress in the zucker obese rat
Ravi Nistala, Javad Habibi, Annayya Aroor, et al.
Journal of Lipid Research
|
March 18, 2004
The ATP-binding cassette transporter 1 mediates lipid efflux from Sertoli cells and influences male fertility
David M Selva, Veronica Hirsch-Reinshagen, Braydon Burgess, et al.
Experimental Neurology
|
September 1, 2005
Ethyl-EPA treatment improves motor dysfunction, but not neurodegeneration in the YAC128 mouse model of Huntington disease
Jeremy M Van Raamsdonk, Jacqueline Pearson, Daniel A Rogers, et al.
Disease-A-Month : DM
|
May 1, 1995
Recognition, assessment, and treatment of anxiety in the critical care patient
R C Bone, W R Hayden, R L Levine, et al.
Page
of 104