Search research articles
Contact Us
Filters
Showing results (71-80 of 104) with videos related to
Page
of 11
Sort By:
Cardiovascular Research
|
September 1, 2001
Fas ligand/Fas-mediated apoptosis in human coronary artery smooth muscle cells: therapeutic implications of fratricidal mode of action
A J Belanger, A Scaria, H Lu, et al.
Cell
|
November 15, 1991
Nucleoside triphosphates are required to open the CFTR chloride channel
M P Anderson, H A Berger, D P Rich, et al.
Nature
|
March 11, 1993
Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties
D N Sheppard, D P Rich, L S Ostedgaard, et al.
Bio/Technology (Nature Publishing Company)
|
January 1, 1992
Production of cystic fibrosis transmembrane conductance regulator in the milk of transgenic mice
P DiTullio, S H Cheng, J Marshall, et al.
Gene Therapy
|
February 1, 2002
Tissue-specific expression of an anti-proliferative hybrid transgene from the human smooth muscle alpha-actin promoter suppresses smooth muscle cell proliferation and neointima formation
K N Wills, T Mano, J B Avanzini, et al.
Journal of Molecular Biology
|
September 15, 1984
Effects of site-directed mutations in the central domain of 16 S ribosomal RNA upon ribosomal protein binding, RNA processing and 30 S subunit assembly
M J Stark, R J Gregory, R L Gourse, et al.
The Journal of Biological Chemistry
|
August 12, 1994
The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel
I L Reisin, A G Prat, E H Abraham, et al.
Journal of Molecular Biology
|
September 15, 1984
Interaction of ribosomal proteins S6, S8, S15 and S18 with the central domain of 16 S ribosomal RNA from Escherichia coli
R J Gregory, M L Zeller, D L Thurlow, et al.
Gene Therapy
|
June 1, 1997
Antibody to CD40 ligand inhibits both humoral and cellular immune responses to adenoviral vectors and facilitates repeated administration to mouse airway
A Scaria, J A St George, R J Gregory, et al.
Cell
|
November 16, 1990
Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis
S H Cheng, R J Gregory, J Marshall, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 104) with videos related to
Sort By:
Page
of 11
Cardiovascular Research
|
September 1, 2001
Fas ligand/Fas-mediated apoptosis in human coronary artery smooth muscle cells: therapeutic implications of fratricidal mode of action
A J Belanger, A Scaria, H Lu, et al.
Cell
|
November 15, 1991
Nucleoside triphosphates are required to open the CFTR chloride channel
M P Anderson, H A Berger, D P Rich, et al.
Nature
|
March 11, 1993
Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties
D N Sheppard, D P Rich, L S Ostedgaard, et al.
Bio/Technology (Nature Publishing Company)
|
January 1, 1992
Production of cystic fibrosis transmembrane conductance regulator in the milk of transgenic mice
P DiTullio, S H Cheng, J Marshall, et al.
Gene Therapy
|
February 1, 2002
Tissue-specific expression of an anti-proliferative hybrid transgene from the human smooth muscle alpha-actin promoter suppresses smooth muscle cell proliferation and neointima formation
K N Wills, T Mano, J B Avanzini, et al.
Journal of Molecular Biology
|
September 15, 1984
Effects of site-directed mutations in the central domain of 16 S ribosomal RNA upon ribosomal protein binding, RNA processing and 30 S subunit assembly
M J Stark, R J Gregory, R L Gourse, et al.
The Journal of Biological Chemistry
|
August 12, 1994
The cystic fibrosis transmembrane conductance regulator is a dual ATP and chloride channel
I L Reisin, A G Prat, E H Abraham, et al.
Journal of Molecular Biology
|
September 15, 1984
Interaction of ribosomal proteins S6, S8, S15 and S18 with the central domain of 16 S ribosomal RNA from Escherichia coli
R J Gregory, M L Zeller, D L Thurlow, et al.
Gene Therapy
|
June 1, 1997
Antibody to CD40 ligand inhibits both humoral and cellular immune responses to adenoviral vectors and facilitates repeated administration to mouse airway
A Scaria, J A St George, R J Gregory, et al.
Cell
|
November 16, 1990
Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis
S H Cheng, R J Gregory, J Marshall, et al.
Page
of 11