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E Tullis

Showing results (51-60 of 72) with videos related to

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Genomics|November 4, 1998
The molecular basis of disease variability among cystic fibrosis patients carrying the 3849+10 kb C-->T mutationO Chiba-Falek, E Kerem, T Shoshani, et al.
Veterinary Ophthalmology|June 15, 2007
Neural precursors isolated from the developing cat brain show retinal integration following transplantation to the retina of the dystrophic catHenry Klassen, Philip H Schwartz, Boback Ziaeian, et al.
American Journal of Respiratory and Critical Care Medicine|February 24, 2001
Infection with Burkholderia cepacia in cystic fibrosis: outcome following lung transplantationC Chaparro, J Maurer, C Gutierrez, et al.
Clinical Biochemistry|May 19, 2009
Does the Macroduct collection system reliably define sweat chloride concentration in subjects with intermediate results?J B Rose, L Ellis, B John, et al.
The Journal of Pediatrics|June 8, 2001
Treatment of vitamin K deficiency in cystic fibrosis: Effectiveness of a daily fat-soluble vitamin combinationD C Wilson, M Rashid, P R Durie, et al.
The Journal of Pediatrics|May 15, 1998
Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurementsD C Wilson, L Ellis, J Zielenski, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|October 13, 2001
Direct and indirect bacterial killing functions of neutrophil defensins in lung explantsG A Porro, J H Lee, J de Azavedo, et al.
Clinical Transplantation|January 29, 2011
Outcomes of patients with cystic fibrosis undergoing lung transplantation with and without cystic fibrosis-associated liver cirrhosisE F Nash, C Volling, C A Gutierrez, et al.
Iscience|October 27, 2021
GluN2B S1303 phosphorylation by CaMKII or DAPK1: no indication for involvement in ischemia or LTPJonathan E Tullis, Olivia R Buonarati, Steven J Coultrap, et al.
Fertility and Sterility|October 31, 1998
Heterogeneity of reproductive tract abnormalities in men with absence of the vas deferens: role of cystic fibrosis transmembrane conductance regulator gene mutationsK Jarvi, S McCallum, J Zielenski, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
Genomics|November 4, 1998
The molecular basis of disease variability among cystic fibrosis patients carrying the 3849+10 kb C-->T mutationO Chiba-Falek, E Kerem, T Shoshani, et al.
Veterinary Ophthalmology|June 15, 2007
Neural precursors isolated from the developing cat brain show retinal integration following transplantation to the retina of the dystrophic catHenry Klassen, Philip H Schwartz, Boback Ziaeian, et al.
American Journal of Respiratory and Critical Care Medicine|February 24, 2001
Infection with Burkholderia cepacia in cystic fibrosis: outcome following lung transplantationC Chaparro, J Maurer, C Gutierrez, et al.
Clinical Biochemistry|May 19, 2009
Does the Macroduct collection system reliably define sweat chloride concentration in subjects with intermediate results?J B Rose, L Ellis, B John, et al.
The Journal of Pediatrics|June 8, 2001
Treatment of vitamin K deficiency in cystic fibrosis: Effectiveness of a daily fat-soluble vitamin combinationD C Wilson, M Rashid, P R Durie, et al.
The Journal of Pediatrics|May 15, 1998
Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurementsD C Wilson, L Ellis, J Zielenski, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|October 13, 2001
Direct and indirect bacterial killing functions of neutrophil defensins in lung explantsG A Porro, J H Lee, J de Azavedo, et al.
Clinical Transplantation|January 29, 2011
Outcomes of patients with cystic fibrosis undergoing lung transplantation with and without cystic fibrosis-associated liver cirrhosisE F Nash, C Volling, C A Gutierrez, et al.
Iscience|October 27, 2021
GluN2B S1303 phosphorylation by CaMKII or DAPK1: no indication for involvement in ischemia or LTPJonathan E Tullis, Olivia R Buonarati, Steven J Coultrap, et al.
Fertility and Sterility|October 31, 1998
Heterogeneity of reproductive tract abnormalities in men with absence of the vas deferens: role of cystic fibrosis transmembrane conductance regulator gene mutationsK Jarvi, S McCallum, J Zielenski, et al.
Pageof 8