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H Miner

Showing results (111-120 of 356) with videos related to

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The Journal of Comparative Neurology|October 21, 2003
Ultrastructural localization of the norepinephrine transporter in superficial and deep layers of the rat prelimbic prefrontal cortex and its spatial relationship to probable dopamine terminalsLeeann H Miner, Sally Schroeter, Randy D Blakely, et al.
Plos One|December 19, 2025
Anticodon-edited tRNA enables translational readthrough of COL4A5 premature termination codonsKohei Omachi, Joseph J Porter, John D Lueck, et al.
Kidney360|December 14, 2022
A COL4A4-G394S Variant and Impaired Collagen IV Trimerization in a Patient with Mild Alport SyndromeJennefer Kohler, Kohei Omachi, Vivek Charu, et al.
American Journal of Physiology. Renal Physiology|May 6, 2016
Albumin contributes to kidney disease progression in Alport syndromeGeorge Jarad, Russell H Knutsen, Robert P Mecham, et al.
The Journal of Comparative Neurology|October 31, 2000
Ultrastructural localization of the serotonin transporter in superficial and deep layers of the rat prelimbic prefrontal cortex and its spatial relationship to dopamine terminalsL H Miner, S Schroeter, R D Blakely, et al.
Developmental Biology|April 5, 2014
DLG1 influences distal ureter maturation via a non-epithelial cell autonomous mechanism involving reduced retinoic acid signaling, Ret expression, and apoptosisSung Tae Kim, Sun-Young Ahn, Wojciech Swat, et al.
Journal of the American Society of Nephrology : JASN|June 23, 2006
A hypomorphic mutation in the mouse laminin alpha5 gene causes polycystic kidney diseaseM Brendan Shannon, Bruce L Patton, Scott J Harvey, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 16, 2009
Glomerular filtration is normal in the absence of both agrin and perlecan-heparan sulfate from the glomerular basement membraneSeth Goldberg, Scott J Harvey, Jeanette Cunningham, et al.
Kidney International|February 10, 2007
Choosing a mouse model to study the molecular pathobiology of Alport glomerulonephritisD Cosgrove, R Kalluri, J H Miner, et al.
Journal of Personality Assessment|April 1, 1992
Ethnic differences on the MMPI Overcontrolled-Hostility ScaleH E Hutton, M H Miner, J R Blades, et al.
Pageof 36

Showing results (111-120 of 356) with videos related to

Sort By:
Pageof 36
The Journal of Comparative Neurology|October 21, 2003
Ultrastructural localization of the norepinephrine transporter in superficial and deep layers of the rat prelimbic prefrontal cortex and its spatial relationship to probable dopamine terminalsLeeann H Miner, Sally Schroeter, Randy D Blakely, et al.
Plos One|December 19, 2025
Anticodon-edited tRNA enables translational readthrough of COL4A5 premature termination codonsKohei Omachi, Joseph J Porter, John D Lueck, et al.
Kidney360|December 14, 2022
A COL4A4-G394S Variant and Impaired Collagen IV Trimerization in a Patient with Mild Alport SyndromeJennefer Kohler, Kohei Omachi, Vivek Charu, et al.
American Journal of Physiology. Renal Physiology|May 6, 2016
Albumin contributes to kidney disease progression in Alport syndromeGeorge Jarad, Russell H Knutsen, Robert P Mecham, et al.
The Journal of Comparative Neurology|October 31, 2000
Ultrastructural localization of the serotonin transporter in superficial and deep layers of the rat prelimbic prefrontal cortex and its spatial relationship to dopamine terminalsL H Miner, S Schroeter, R D Blakely, et al.
Developmental Biology|April 5, 2014
DLG1 influences distal ureter maturation via a non-epithelial cell autonomous mechanism involving reduced retinoic acid signaling, Ret expression, and apoptosisSung Tae Kim, Sun-Young Ahn, Wojciech Swat, et al.
Journal of the American Society of Nephrology : JASN|June 23, 2006
A hypomorphic mutation in the mouse laminin alpha5 gene causes polycystic kidney diseaseM Brendan Shannon, Bruce L Patton, Scott J Harvey, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 16, 2009
Glomerular filtration is normal in the absence of both agrin and perlecan-heparan sulfate from the glomerular basement membraneSeth Goldberg, Scott J Harvey, Jeanette Cunningham, et al.
Kidney International|February 10, 2007
Choosing a mouse model to study the molecular pathobiology of Alport glomerulonephritisD Cosgrove, R Kalluri, J H Miner, et al.
Journal of Personality Assessment|April 1, 1992
Ethnic differences on the MMPI Overcontrolled-Hostility ScaleH E Hutton, M H Miner, J R Blades, et al.
Pageof 36