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Bruce A Hamilton

Showing results (21-30 of 57) with videos related to

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Human Molecular Genetics|July 7, 2011
Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient miceWendy A Alcaraz, Edward Chen, Phoebe Valdes, et al.
Journal of Human Genetics|May 2, 2006
Analyses of 5' regulatory region polymorphisms in human SLC22A6 (OAT1) and SLC22A8 (OAT3)Vibha Bhatnagar, Gang Xu, Bruce A Hamilton, et al.
Plos One|June 14, 2013
Zfp423 binds autoregulatory sites in p19 cell culture modelYoung-Wook Cho, Chen-Jei Hong, Aiju Hou, et al.
Molecular Pharmacology|August 25, 2004
The catecholamine release-inhibitory "catestatin" fragment of chromogranin a: naturally occurring human variants with different potencies for multiple chromaffin cell nicotinic cholinergic responsesSushil K Mahata, Manjula Mahata, Gen Wen, et al.
Developmental Biology|January 7, 2018
TBR2 antagonizes retinoic acid dependent neuronal differentiation by repressing Zfp423 during corticogenesisLuca Massimino, Lisbeth Flores-Garcia, Bruno Di Stefano, et al.
Plos Genetics|October 15, 2025
Tulp3 quantitative alleles titrate requirements for viability, brain development, and kidney homeostasis but do not suppress Zfp423 mutations in miceCorinne A McCoy, Dorothy Concepcion, Mark G Mezody, et al.
Biorxiv : the Preprint Server for Biology|May 13, 2026
<i>Mysm1</i> mutations in <i>meander tail</i> mice cause anterior-selective cerebellum malformationBruce A Hamilton, Dorothy Concepcion, Max Chang, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
<i>Tulp3</i> quantitative alleles titrate requirements for viability, brain development, and kidney homeostasis but do not suppress <i>Zfp423</i> mutations in miceCorinne A McCoy, Dorothy Concepcion, Mark G Mezody, et al.
The Journal of Biological Chemistry|June 6, 2003
Mice lacking phosphatidylinositol transfer protein-alpha exhibit spinocerebellar degeneration, intestinal and hepatic steatosis, and hypoglycemiaJames G Alb, Jorge D Cortese, Scott E Phillips, et al.
Neuron|December 23, 2003
RORalpha coordinates reciprocal signaling in cerebellar development through sonic hedgehog and calcium-dependent pathwaysDavid A Gold, Sung Hee Baek, Nicholas J Schork, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|July 7, 2011
Modifier genes and non-genetic factors reshape anatomical deficits in Zfp423-deficient miceWendy A Alcaraz, Edward Chen, Phoebe Valdes, et al.
Journal of Human Genetics|May 2, 2006
Analyses of 5' regulatory region polymorphisms in human SLC22A6 (OAT1) and SLC22A8 (OAT3)Vibha Bhatnagar, Gang Xu, Bruce A Hamilton, et al.
Plos One|June 14, 2013
Zfp423 binds autoregulatory sites in p19 cell culture modelYoung-Wook Cho, Chen-Jei Hong, Aiju Hou, et al.
Molecular Pharmacology|August 25, 2004
The catecholamine release-inhibitory "catestatin" fragment of chromogranin a: naturally occurring human variants with different potencies for multiple chromaffin cell nicotinic cholinergic responsesSushil K Mahata, Manjula Mahata, Gen Wen, et al.
Developmental Biology|January 7, 2018
TBR2 antagonizes retinoic acid dependent neuronal differentiation by repressing Zfp423 during corticogenesisLuca Massimino, Lisbeth Flores-Garcia, Bruno Di Stefano, et al.
Plos Genetics|October 15, 2025
Tulp3 quantitative alleles titrate requirements for viability, brain development, and kidney homeostasis but do not suppress Zfp423 mutations in miceCorinne A McCoy, Dorothy Concepcion, Mark G Mezody, et al.
Biorxiv : the Preprint Server for Biology|May 13, 2026
<i>Mysm1</i> mutations in <i>meander tail</i> mice cause anterior-selective cerebellum malformationBruce A Hamilton, Dorothy Concepcion, Max Chang, et al.
Biorxiv : the Preprint Server for Biology|September 26, 2025
<i>Tulp3</i> quantitative alleles titrate requirements for viability, brain development, and kidney homeostasis but do not suppress <i>Zfp423</i> mutations in miceCorinne A McCoy, Dorothy Concepcion, Mark G Mezody, et al.
The Journal of Biological Chemistry|June 6, 2003
Mice lacking phosphatidylinositol transfer protein-alpha exhibit spinocerebellar degeneration, intestinal and hepatic steatosis, and hypoglycemiaJames G Alb, Jorge D Cortese, Scott E Phillips, et al.
Neuron|December 23, 2003
RORalpha coordinates reciprocal signaling in cerebellar development through sonic hedgehog and calcium-dependent pathwaysDavid A Gold, Sung Hee Baek, Nicholas J Schork, et al.
Pageof 6