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Tertius A Hough

Showing results (11-20 of 27) with videos related to

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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 2, 2007
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2Tertius A Hough, Monika Polewski, Kristen Johnson, et al.
Plos One|April 2, 2015
Pharmacological inhibition of FTOFiona McMurray, Marina Demetriades, WeiShen Aik, et al.
Journal of Pharmacological and Toxicological Methods|May 16, 2019
Drug safety Africa: An overview of safety pharmacology & toxicology in South AfricaBrian D Guth, Anne F Grobler, Kendall S Frazier, et al.
Plos Genetics|October 27, 2011
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutantsMichael T Cheeseman, Hayley E Tyrer, Debbie Williams, et al.
Plos One|August 23, 2012
A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosisChristopher T Esapa, Rosie A Head, Jeshmi Jeyabalan, et al.
JCI Insight|February 15, 2017
G<b>α</b><sub>11</sub> mutation in mice causes hypocalcemia rectifiable by calcilytic therapyCaroline M Gorvin, Fadil M Hannan, Sarah A Howles, et al.
Plos Genetics|October 13, 2006
Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis mediaNicholas Parkinson, Rachel E Hardisty-Hughes, Hilda Tateossian, et al.
Endocrinology|December 5, 2013
An N-ethyl-N-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excessLiz Bentley, Christopher T Esapa, M Andrew Nesbit, et al.
Endocrinology|June 3, 2017
Mutant Mice With Calcium-Sensing Receptor Activation Have Hyperglycemia That Is Rectified by Calcilytic TherapyValerie N Babinsky, Fadil M Hannan, Reshma D Ramracheya, et al.
Plos One|February 6, 2013
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5Nellie Y Loh, Liz Bentley, Henrik Dimke, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 2, 2007
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2Tertius A Hough, Monika Polewski, Kristen Johnson, et al.
Plos One|April 2, 2015
Pharmacological inhibition of FTOFiona McMurray, Marina Demetriades, WeiShen Aik, et al.
Journal of Pharmacological and Toxicological Methods|May 16, 2019
Drug safety Africa: An overview of safety pharmacology & toxicology in South AfricaBrian D Guth, Anne F Grobler, Kendall S Frazier, et al.
Plos Genetics|October 27, 2011
HIF-VEGF pathways are critical for chronic otitis media in Junbo and Jeff mouse mutantsMichael T Cheeseman, Hayley E Tyrer, Debbie Williams, et al.
Plos One|August 23, 2012
A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosisChristopher T Esapa, Rosie A Head, Jeshmi Jeyabalan, et al.
JCI Insight|February 15, 2017
G<b>α</b><sub>11</sub> mutation in mice causes hypocalcemia rectifiable by calcilytic therapyCaroline M Gorvin, Fadil M Hannan, Sarah A Howles, et al.
Plos Genetics|October 13, 2006
Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis mediaNicholas Parkinson, Rachel E Hardisty-Hughes, Hilda Tateossian, et al.
Endocrinology|December 5, 2013
An N-ethyl-N-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excessLiz Bentley, Christopher T Esapa, M Andrew Nesbit, et al.
Endocrinology|June 3, 2017
Mutant Mice With Calcium-Sensing Receptor Activation Have Hyperglycemia That Is Rectified by Calcilytic TherapyValerie N Babinsky, Fadil M Hannan, Reshma D Ramracheya, et al.
Plos One|February 6, 2013
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5Nellie Y Loh, Liz Bentley, Henrik Dimke, et al.
Pageof 3