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Showing results (731-740 of 866) with videos related to

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Matrix Biology Plus|October 25, 2021
Deletion of type VIII collagen reduces blood pressure, increases carotid artery functional distensibility and promotes elastin depositionAmanda L Mohabeer, Jeffrey T Kroetsch, Meghan McFadden, et al.
JCI Insight|October 7, 2025
CRISPR/Cas-mediated activation of genes associated with inherited retinal dystrophies in human cells for diagnostic purposesValentin J Weber, Alice Reschigna, Maximilian J Gerhardt, et al.
American Journal of Human Genetics|March 1, 2011
Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfectaJutta Becker, Oliver Semler, Christian Gilissen, et al.
Gastrointestinal Endoscopy|June 4, 2005
A prospective two-center study comparing wireless capsule endoscopy with intraoperative enteroscopy in patients with obscure GI bleedingDirk Hartmann, Harald Schmidt, Georg Bolz, et al.
American Journal of Respiratory and Critical Care Medicine|July 14, 2015
Evolution of Diaphragm Thickness during Mechanical Ventilation. Impact of Inspiratory EffortEwan C Goligher, Eddy Fan, Margaret S Herridge, et al.
The Journal of Clinical Investigation|June 3, 2011
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamicsClaudia Dafinger, Max Christoph Liebau, Solaf Mohamed Elsayed, et al.
Orphanet Journal of Rare Diseases|April 12, 2022
Designing rare disease care pathways in the Republic of Ireland: a co-operative modelA J Ward, D Murphy, R Marron, et al.
Nature Neuroscience|December 7, 2010
Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessShahid M Baig, Alexandra Koschak, Andreas Lieb, et al.
American Journal of Human Genetics|August 21, 2012
A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsiaSusanne Kohl, Frauke Coppieters, Françoise Meire, et al.
The Journal of Clinical Investigation|May 5, 2010
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndromeInga Ebermann, Jennifer B Phillips, Max C Liebau, et al.
Pageof 87

Showing results (731-740 of 866) with videos related to

Sort By:
Pageof 87
Matrix Biology Plus|October 25, 2021
Deletion of type VIII collagen reduces blood pressure, increases carotid artery functional distensibility and promotes elastin depositionAmanda L Mohabeer, Jeffrey T Kroetsch, Meghan McFadden, et al.
JCI Insight|October 7, 2025
CRISPR/Cas-mediated activation of genes associated with inherited retinal dystrophies in human cells for diagnostic purposesValentin J Weber, Alice Reschigna, Maximilian J Gerhardt, et al.
American Journal of Human Genetics|March 1, 2011
Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfectaJutta Becker, Oliver Semler, Christian Gilissen, et al.
Gastrointestinal Endoscopy|June 4, 2005
A prospective two-center study comparing wireless capsule endoscopy with intraoperative enteroscopy in patients with obscure GI bleedingDirk Hartmann, Harald Schmidt, Georg Bolz, et al.
American Journal of Respiratory and Critical Care Medicine|July 14, 2015
Evolution of Diaphragm Thickness during Mechanical Ventilation. Impact of Inspiratory EffortEwan C Goligher, Eddy Fan, Margaret S Herridge, et al.
The Journal of Clinical Investigation|June 3, 2011
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamicsClaudia Dafinger, Max Christoph Liebau, Solaf Mohamed Elsayed, et al.
Orphanet Journal of Rare Diseases|April 12, 2022
Designing rare disease care pathways in the Republic of Ireland: a co-operative modelA J Ward, D Murphy, R Marron, et al.
Nature Neuroscience|December 7, 2010
Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafnessShahid M Baig, Alexandra Koschak, Andreas Lieb, et al.
American Journal of Human Genetics|August 21, 2012
A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsiaSusanne Kohl, Frauke Coppieters, Françoise Meire, et al.
The Journal of Clinical Investigation|May 5, 2010
PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndromeInga Ebermann, Jennifer B Phillips, Max C Liebau, et al.
Pageof 87