Search research articles
Contact Us
Filters
Showing results (261-270 of 323) with videos related to
Page
of 33
Sort By:
Biochemical Pharmacology
|
January 27, 1999
Induction of human breast cancer cell apoptosis from G2/M preceded by stimulation into the cell cycle by Z-1,1-dichloro-2,3-diphenylcyclopropane
R Balachandran, E ter Haar, J C Yalowich, et al.
The Journal of Biological Chemistry
|
March 7, 1997
Complexes of adenovirus with polycationic polymers and cationic lipids increase the efficiency of gene transfer in vitro and in vivo
A Fasbender, J Zabner, M Chillón, et al.
The Journal of Clinical Investigation
|
December 1, 1995
rENaC is the predominant Na+ channel in the apical membrane of the rat renal inner medullary collecting duct
K A Volk, R D Sigmund, P M Snyder, et al.
Indiana Medicine : the Journal of the Indiana State Medical Association
|
June 1, 1989
Stone babies still occur
J E Gilliland, D R Wippermann, M E Pauszek, et al.
Cell
|
April 23, 1993
Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast
J L Teem, H A Berger, L S Ostedgaard, et al.
The Journal of Cell Biology
|
February 14, 1998
Ripped pocket and pickpocket, novel Drosophila DEG/ENaC subunits expressed in early development and in mechanosensory neurons
C M Adams, M G Anderson, D G Motto, et al.
Nature
|
October 26, 2000
Quorum-sensing signals indicate that cystic fibrosis lungs are infected with bacterial biofilms
P K Singh, A L Schaefer, M R Parsek, et al.
Annual Review of Physiology
|
January 1, 1980
Regulation of the testis sertoli cell by follicle stimulating hormone
A R Means, J R Dedman, J S Tash, 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.
Page
of 33
Search research articles
Search
Showing results (261-270 of 323) with videos related to
Sort By:
Page
of 33
Biochemical Pharmacology
|
January 27, 1999
Induction of human breast cancer cell apoptosis from G2/M preceded by stimulation into the cell cycle by Z-1,1-dichloro-2,3-diphenylcyclopropane
R Balachandran, E ter Haar, J C Yalowich, et al.
The Journal of Biological Chemistry
|
March 7, 1997
Complexes of adenovirus with polycationic polymers and cationic lipids increase the efficiency of gene transfer in vitro and in vivo
A Fasbender, J Zabner, M Chillón, et al.
The Journal of Clinical Investigation
|
December 1, 1995
rENaC is the predominant Na+ channel in the apical membrane of the rat renal inner medullary collecting duct
K A Volk, R D Sigmund, P M Snyder, et al.
Indiana Medicine : the Journal of the Indiana State Medical Association
|
June 1, 1989
Stone babies still occur
J E Gilliland, D R Wippermann, M E Pauszek, et al.
Cell
|
April 23, 1993
Identification of revertants for the cystic fibrosis delta F508 mutation using STE6-CFTR chimeras in yeast
J L Teem, H A Berger, L S Ostedgaard, et al.
The Journal of Cell Biology
|
February 14, 1998
Ripped pocket and pickpocket, novel Drosophila DEG/ENaC subunits expressed in early development and in mechanosensory neurons
C M Adams, M G Anderson, D G Motto, et al.
Nature
|
October 26, 2000
Quorum-sensing signals indicate that cystic fibrosis lungs are infected with bacterial biofilms
P K Singh, A L Schaefer, M R Parsek, et al.
Annual Review of Physiology
|
January 1, 1980
Regulation of the testis sertoli cell by follicle stimulating hormone
A R Means, J R Dedman, J S Tash, 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.
Page
of 33