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M Andrew

Showing results (671-680 of 703) with videos related to

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Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Journal of Neuroinflammation|November 4, 2024
Shifts in the spatiotemporal profile of inflammatory phenotypes of innate immune cells in the rat brain following acute intoxication with the organophosphate diisopropylfluorophosphatePeter M Andrew, Jeremy A MacMahon, Pedro N Bernardino, et al.
Pediatric Research|June 1, 2000
Outcome of pediatric thromboembolic disease: a report from the Canadian Childhood Thrombophilia RegistryP Monagle, M Adams, M Mahoney, 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.
The American Journal of Forensic Medicine and Pathology|November 29, 2007
Guidelines for postmortem protocol for ocular investigation of sudden unexplained infant death and suspected physical child abuseM G F Gilliland, Alex V Levin, Robert W Enzenauer, et al.
JACC. Heart Failure|September 13, 2024
Evaluating Mitral TEER in the Management of Moderate Secondary Mitral Regurgitation Among Heart Failure PatientsAnita W Asgar, Gilbert H L Tang, Jason H Rogers, et al.
Experimental Eye Research|October 27, 2018
A novel role for CRIM1 in the corneal response to UV and pterygium developmentEleonora Maurizi, Davide Schiroli, Sarah D Atkinson, 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.
The Journal of Clinical Investigation|May 21, 2010
Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2Irina V Grigorieva, Samantha Mirczuk, Katherine U Gaynor, et al.
JBMR Plus|October 5, 2018
An <i>N</i>-Ethyl-<i>N</i>-Nitrosourea (ENU) Mutagenized Mouse Model for Autosomal Dominant Nonsyndromic Kyphoscoliosis Due to Vertebral FusionChristopher T Esapa, Sian E Piret, M Andrew Nesbit, et al.
Pageof 71

Showing results (671-680 of 703) with videos related to

Sort By:
Pageof 71
Nature Genetics|December 11, 2012
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, et al.
Journal of Neuroinflammation|November 4, 2024
Shifts in the spatiotemporal profile of inflammatory phenotypes of innate immune cells in the rat brain following acute intoxication with the organophosphate diisopropylfluorophosphatePeter M Andrew, Jeremy A MacMahon, Pedro N Bernardino, et al.
Pediatric Research|June 1, 2000
Outcome of pediatric thromboembolic disease: a report from the Canadian Childhood Thrombophilia RegistryP Monagle, M Adams, M Mahoney, 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.
The American Journal of Forensic Medicine and Pathology|November 29, 2007
Guidelines for postmortem protocol for ocular investigation of sudden unexplained infant death and suspected physical child abuseM G F Gilliland, Alex V Levin, Robert W Enzenauer, et al.
JACC. Heart Failure|September 13, 2024
Evaluating Mitral TEER in the Management of Moderate Secondary Mitral Regurgitation Among Heart Failure PatientsAnita W Asgar, Gilbert H L Tang, Jason H Rogers, et al.
Experimental Eye Research|October 27, 2018
A novel role for CRIM1 in the corneal response to UV and pterygium developmentEleonora Maurizi, Davide Schiroli, Sarah D Atkinson, 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.
The Journal of Clinical Investigation|May 21, 2010
Gata3-deficient mice develop parathyroid abnormalities due to dysregulation of the parathyroid-specific transcription factor Gcm2Irina V Grigorieva, Samantha Mirczuk, Katherine U Gaynor, et al.
JBMR Plus|October 5, 2018
An <i>N</i>-Ethyl-<i>N</i>-Nitrosourea (ENU) Mutagenized Mouse Model for Autosomal Dominant Nonsyndromic Kyphoscoliosis Due to Vertebral FusionChristopher T Esapa, Sian E Piret, M Andrew Nesbit, et al.
Pageof 71