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R J Gregory

Showing results (71-80 of 104) with videos related to

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Cardiovascular Research|September 1, 2001
Fas ligand/Fas-mediated apoptosis in human coronary artery smooth muscle cells: therapeutic implications of fratricidal mode of actionA J Belanger, A Scaria, H Lu, et al.
Cell|November 15, 1991
Nucleoside triphosphates are required to open the CFTR chloride channelM 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 propertiesD 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 miceP 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 formationK 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 assemblyM 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 channelI 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 coliR 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 airwayA 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 fibrosisS H Cheng, R J Gregory, J Marshall, et al.
Pageof 11

Showing results (71-80 of 104) with videos related to

Sort By:
Pageof 11
Cardiovascular Research|September 1, 2001
Fas ligand/Fas-mediated apoptosis in human coronary artery smooth muscle cells: therapeutic implications of fratricidal mode of actionA J Belanger, A Scaria, H Lu, et al.
Cell|November 15, 1991
Nucleoside triphosphates are required to open the CFTR chloride channelM 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 propertiesD 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 miceP 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 formationK 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 assemblyM 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 channelI 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 coliR 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 airwayA 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 fibrosisS H Cheng, R J Gregory, J Marshall, et al.
Pageof 11