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Mitchell L Drumm

Showing results (21-30 of 70) with videos related to

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American Journal of Physiology. Gastrointestinal and Liver Physiology|June 9, 2012
Altered de novo lipogenesis contributes to low adipose stores in cystic fibrosis miceIlya Bederman, Aura Perez, Leigh Henderson, et al.
Nature Reviews. Disease Primers|September 7, 2023
Glycogen storage diseasesWilliam B Hannah, Terry G J Derks, Mitchell L Drumm, et al.
American Journal of Respiratory Cell and Molecular Biology|April 7, 2009
INO-4995 therapeutic efficacy is enhanced with repeat dosing in cystic fibrosis knockout mice and human epitheliaAlexis E Traynor-Kaplan, Mark Moody, Magda Nur, et al.
Clinical and Experimental Gastroenterology|February 13, 2015
Effect of genistein on basal jejunal chloride secretion in R117H CF mice is sex and route specificEsa Rayyan, Sarah Polito, Lana Leung, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 8, 2013
Ventilatory pattern and energy expenditure are altered in cystic fibrosis miceRebecca J Darrah, Ilya R Bederman, Anna L Mitchell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2016
A novel guluronate oligomer improves intestinal transit and survival in cystic fibrosis miceMegan Vitko, Dana M Valerio, Philip D Rye, et al.
Physiological Genomics|May 12, 2020
Functional genomics analysis of human colon organoids identifies key transcription factorsShiyi Yin, Greeshma Ray, Jenny L Kerschner, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|September 7, 2018
Small adipose stores in cystic fibrosis mice are characterized by reduced cell volume, not cell numberIlya Bederman, Alex DiScenna, Leigh Henderson, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 28, 2016
Early pulmonary disease manifestations in cystic fibrosis miceRebecca J Darrah, Anna L Mitchell, Cara K Campanaro, et al.
Pediatric Pulmonology|April 5, 2005
Beta 2 adrenergic receptor polymorphisms in cystic fibrosisMeeghan A Hart, Michael W Konstan, Rebecca J Darrah, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
American Journal of Physiology. Gastrointestinal and Liver Physiology|June 9, 2012
Altered de novo lipogenesis contributes to low adipose stores in cystic fibrosis miceIlya Bederman, Aura Perez, Leigh Henderson, et al.
Nature Reviews. Disease Primers|September 7, 2023
Glycogen storage diseasesWilliam B Hannah, Terry G J Derks, Mitchell L Drumm, et al.
American Journal of Respiratory Cell and Molecular Biology|April 7, 2009
INO-4995 therapeutic efficacy is enhanced with repeat dosing in cystic fibrosis knockout mice and human epitheliaAlexis E Traynor-Kaplan, Mark Moody, Magda Nur, et al.
Clinical and Experimental Gastroenterology|February 13, 2015
Effect of genistein on basal jejunal chloride secretion in R117H CF mice is sex and route specificEsa Rayyan, Sarah Polito, Lana Leung, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 8, 2013
Ventilatory pattern and energy expenditure are altered in cystic fibrosis miceRebecca J Darrah, Ilya R Bederman, Anna L Mitchell, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 26, 2016
A novel guluronate oligomer improves intestinal transit and survival in cystic fibrosis miceMegan Vitko, Dana M Valerio, Philip D Rye, et al.
Physiological Genomics|May 12, 2020
Functional genomics analysis of human colon organoids identifies key transcription factorsShiyi Yin, Greeshma Ray, Jenny L Kerschner, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|September 7, 2018
Small adipose stores in cystic fibrosis mice are characterized by reduced cell volume, not cell numberIlya Bederman, Alex DiScenna, Leigh Henderson, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 28, 2016
Early pulmonary disease manifestations in cystic fibrosis miceRebecca J Darrah, Anna L Mitchell, Cara K Campanaro, et al.
Pediatric Pulmonology|April 5, 2005
Beta 2 adrenergic receptor polymorphisms in cystic fibrosisMeeghan A Hart, Michael W Konstan, Rebecca J Darrah, et al.
Pageof 7