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Bradley K Yoder

Showing results (81-90 of 124) with videos related to

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Laboratory Investigation; a Journal of Technical Methods and Pathology|June 23, 2021
Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic diseaseKurt A Zimmerman, Cheng J Song, Ernald J G Aloria, et al.
Plos Genetics|February 11, 2016
A Screen for Modifiers of Cilia Phenotypes Reveals Novel MKS Alleles and Uncovers a Specific Genetic Interaction between osm-3 and nphp-4Svetlana V Masyukova, Dawn E Landis, Scott J Henke, et al.
Current Biology : CB|September 11, 2007
Disruption of intraflagellar transport in adult mice leads to obesity and slow-onset cystic kidney diseaseJames R Davenport, Amanda J Watts, Venus C Roper, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2013
Leptin resistance is a secondary consequence of the obesity in ciliopathy mutant miceNicolas F Berbari, Raymond C Pasek, Erik B Malarkey, et al.
Circulation Research|March 12, 2011
Lack of primary cilia primes shear-induced endothelial-to-mesenchymal transitionAnastasia D Egorova, Padmini P S J Khedoe, Marie-José T H Goumans, et al.
American Journal of Physiology. Renal Physiology|January 7, 2006
Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cellsBrian J Siroky, William B Ferguson, Amanda L Fuson, et al.
Human Molecular Genetics|February 9, 2021
A mouse model of BBS identifies developmental and homeostatic effects of BBS5 mutation and identifies novel pituitary abnormalitiesMelissa R Bentley-Ford, Staci E Engle, Kelsey R Clearman, et al.
Genetics|December 1, 2021
Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypesMelissa R Bentley-Ford, Melissa LaBonty, Holly R Thomas, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|March 17, 2021
A transgenic Alx4-CreER mouse to analyze anterior limb and nephric duct developmentDevan M Rockwell, Amber K O'Connor, Melissa R Bentley-Ford, et al.
American Journal of Physiology. Renal Physiology|February 16, 2023
Accuracy and processing time of kidney volume measurement methods in rodents polycystic kidney disease models: superiority of semiautomated kidney segmentationMary Claire Doss, Sean Mullen, Ronald Roye, et al.
Pageof 13

Showing results (81-90 of 124) with videos related to

Sort By:
Pageof 13
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 23, 2021
Early infiltrating macrophage subtype correlates with late-stage phenotypic outcome in a mouse model of hepatorenal fibrocystic diseaseKurt A Zimmerman, Cheng J Song, Ernald J G Aloria, et al.
Plos Genetics|February 11, 2016
A Screen for Modifiers of Cilia Phenotypes Reveals Novel MKS Alleles and Uncovers a Specific Genetic Interaction between osm-3 and nphp-4Svetlana V Masyukova, Dawn E Landis, Scott J Henke, et al.
Current Biology : CB|September 11, 2007
Disruption of intraflagellar transport in adult mice leads to obesity and slow-onset cystic kidney diseaseJames R Davenport, Amanda J Watts, Venus C Roper, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2013
Leptin resistance is a secondary consequence of the obesity in ciliopathy mutant miceNicolas F Berbari, Raymond C Pasek, Erik B Malarkey, et al.
Circulation Research|March 12, 2011
Lack of primary cilia primes shear-induced endothelial-to-mesenchymal transitionAnastasia D Egorova, Padmini P S J Khedoe, Marie-José T H Goumans, et al.
American Journal of Physiology. Renal Physiology|January 7, 2006
Loss of primary cilia results in deregulated and unabated apical calcium entry in ARPKD collecting duct cellsBrian J Siroky, William B Ferguson, Amanda L Fuson, et al.
Human Molecular Genetics|February 9, 2021
A mouse model of BBS identifies developmental and homeostatic effects of BBS5 mutation and identifies novel pituitary abnormalitiesMelissa R Bentley-Ford, Staci E Engle, Kelsey R Clearman, et al.
Genetics|December 1, 2021
Evolutionarily conserved genetic interactions between nphp-4 and bbs-5 mutations exacerbate ciliopathy phenotypesMelissa R Bentley-Ford, Melissa LaBonty, Holly R Thomas, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|March 17, 2021
A transgenic Alx4-CreER mouse to analyze anterior limb and nephric duct developmentDevan M Rockwell, Amber K O'Connor, Melissa R Bentley-Ford, et al.
American Journal of Physiology. Renal Physiology|February 16, 2023
Accuracy and processing time of kidney volume measurement methods in rodents polycystic kidney disease models: superiority of semiautomated kidney segmentationMary Claire Doss, Sean Mullen, Ronald Roye, et al.
Pageof 13