S E Wert - JoVE Visualize

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Proceedings of the National Academy of Sciences of the United States of America|May 10, 2000

Increased metalloproteinase activity, oxidant production, and emphysema in surfactant protein D gene-inactivated miceS E Wert, M Yoshida, A M LeVine, et al.

Pediatric Research|August 29, 2000

Prolonged survival in hereditary surfactant protein B (SP-B) deficiency associated with a novel splicing mutationA E Dunbar, S E Wert, M Ikegami, et al.

Human Pathology|June 22, 1999

Congenital cystic adenomatoid malformation of the lung (CCAM): evaluation of the cellular componentsR A Morotti, J Cangiarella, M C Gutierrez, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 19, 1995

Pulmonary malformation in transgenic mice expressing human keratinocyte growth factor in the lungW S Simonet, M L DeRose, N Bucay, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 1, 1990

Cis-acting sequences from a human surfactant protein gene confer pulmonary-specific gene expression in transgenic miceT R Korfhagen, S W Glasser, S E Wert, et al.

The Journal of Biological Chemistry|July 25, 1992

cis-acting elements that confer lung epithelial cell expression of the CC10 geneB R Stripp, P L Sawaya, D S Luse, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 15, 2001

Aquaporin 5-deficient mouse lungs are hyperresponsive to cholinergic stimulationC M Krane, C N Fortner, A R Hand, et al.

Nature Genetics|September 1, 1992

Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic miceJ A Whitsett, C R Dey, B R Stripp, et al.

The Journal of Biological Chemistry|October 17, 1998

Surfactant protein-D regulates surfactant phospholipid homeostasis in vivoT R Korfhagen, V Sheftelyevich, M S Burhans, et al.

Human Gene Therapy|February 10, 1996

Safety of adenovirus-mediated transfer of the human cystic fibrosis transmembrane conductance regulator cDNA to the lungs of nonhuman primatesR W Wilmott, R S Amin, C R Perez, et al.

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Showing results (51-60 of 61) with videos related to

Sort By:

Pageof 7

Proceedings of the National Academy of Sciences of the United States of America|May 10, 2000

Increased metalloproteinase activity, oxidant production, and emphysema in surfactant protein D gene-inactivated miceS E Wert, M Yoshida, A M LeVine, et al.

Pediatric Research|August 29, 2000

Prolonged survival in hereditary surfactant protein B (SP-B) deficiency associated with a novel splicing mutationA E Dunbar, S E Wert, M Ikegami, et al.

Human Pathology|June 22, 1999

Congenital cystic adenomatoid malformation of the lung (CCAM): evaluation of the cellular componentsR A Morotti, J Cangiarella, M C Gutierrez, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 19, 1995

Pulmonary malformation in transgenic mice expressing human keratinocyte growth factor in the lungW S Simonet, M L DeRose, N Bucay, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 1, 1990

Cis-acting sequences from a human surfactant protein gene confer pulmonary-specific gene expression in transgenic miceT R Korfhagen, S W Glasser, S E Wert, et al.

The Journal of Biological Chemistry|July 25, 1992

cis-acting elements that confer lung epithelial cell expression of the CC10 geneB R Stripp, P L Sawaya, D S Luse, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 15, 2001

Aquaporin 5-deficient mouse lungs are hyperresponsive to cholinergic stimulationC M Krane, C N Fortner, A R Hand, et al.

Nature Genetics|September 1, 1992

Human cystic fibrosis transmembrane conductance regulator directed to respiratory epithelial cells of transgenic miceJ A Whitsett, C R Dey, B R Stripp, et al.

The Journal of Biological Chemistry|October 17, 1998

Surfactant protein-D regulates surfactant phospholipid homeostasis in vivoT R Korfhagen, V Sheftelyevich, M S Burhans, et al.

Human Gene Therapy|February 10, 1996

Safety of adenovirus-mediated transfer of the human cystic fibrosis transmembrane conductance regulator cDNA to the lungs of nonhuman primatesR W Wilmott, R S Amin, C R Perez, et al.

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