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Journal of the American Association for Laboratory Animal Science : JAALAS
|
May 30, 2009
Urethral obstruction by seminal coagulum is associated with medetomidine-ketamine anesthesia in male mice on C57BL/6J and mixed genetic backgrounds
Sara Wells, Chris Trower, Tertius A Hough, et al.
Journal of Proteome Research
|
April 8, 2015
¹H NMR metabolic profiling of plasma reveals additional phenotypes in knockout mouse models
Fay Probert, Paul Rice, Cheryl L Scudamore, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 7, 2004
Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification
Tertius A Hough, Debora Bogani, Michael T Cheeseman, et al.
Plos One
|
January 4, 2013
A mouse model for osseous heteroplasia
Michael T Cheeseman, Kate Vowell, Tertius A Hough, et al.
Disease Models & Mechanisms
|
March 23, 2017
A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress
Sian E Piret, Eric Olinger, Anita A C Reed, et al.
JBMR Plus
|
February 27, 2018
N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (<i>Ap2s1</i>) Mutations Establish <i>Ap2s1</i> Loss-of-Function Mice
Caroline M Gorvin, Angela Rogers, Michelle Stewart, et al.
Biology Open
|
October 4, 2015
Loss of arylformamidase with reduced thymidine kinase expression leads to impaired glucose tolerance
Alison J Hugill, Michelle E Stewart, Marianne A Yon, et al.
Endocrinology
|
June 9, 2015
The Calcilytic Agent NPS 2143 Rectifies Hypocalcemia in a Mouse Model With an Activating Calcium-Sensing Receptor (CaSR) Mutation: Relevance to Autosomal Dominant Hypocalcemia Type 1 (ADH1)
Fadil M Hannan, Gerard V Walls, Valerie N Babinsky, et al.
The Journal of Pathology
|
December 3, 2013
Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome
Katherine R Bull, Thomas Mason, Andrew J Rimmer, et al.
JCI Insight
|
October 20, 2017
Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation
Sarah A Howles, Fadil M Hannan, Caroline M Gorvin, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 27) with videos related to
Sort By:
Page
of 3
Journal of the American Association for Laboratory Animal Science : JAALAS
|
May 30, 2009
Urethral obstruction by seminal coagulum is associated with medetomidine-ketamine anesthesia in male mice on C57BL/6J and mixed genetic backgrounds
Sara Wells, Chris Trower, Tertius A Hough, et al.
Journal of Proteome Research
|
April 8, 2015
¹H NMR metabolic profiling of plasma reveals additional phenotypes in knockout mouse models
Fay Probert, Paul Rice, Cheryl L Scudamore, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 7, 2004
Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification
Tertius A Hough, Debora Bogani, Michael T Cheeseman, et al.
Plos One
|
January 4, 2013
A mouse model for osseous heteroplasia
Michael T Cheeseman, Kate Vowell, Tertius A Hough, et al.
Disease Models & Mechanisms
|
March 23, 2017
A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stress
Sian E Piret, Eric Olinger, Anita A C Reed, et al.
JBMR Plus
|
February 27, 2018
N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (<i>Ap2s1</i>) Mutations Establish <i>Ap2s1</i> Loss-of-Function Mice
Caroline M Gorvin, Angela Rogers, Michelle Stewart, et al.
Biology Open
|
October 4, 2015
Loss of arylformamidase with reduced thymidine kinase expression leads to impaired glucose tolerance
Alison J Hugill, Michelle E Stewart, Marianne A Yon, et al.
Endocrinology
|
June 9, 2015
The Calcilytic Agent NPS 2143 Rectifies Hypocalcemia in a Mouse Model With an Activating Calcium-Sensing Receptor (CaSR) Mutation: Relevance to Autosomal Dominant Hypocalcemia Type 1 (ADH1)
Fadil M Hannan, Gerard V Walls, Valerie N Babinsky, et al.
The Journal of Pathology
|
December 3, 2013
Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome
Katherine R Bull, Thomas Mason, Andrew J Rimmer, et al.
JCI Insight
|
October 20, 2017
Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation
Sarah A Howles, Fadil M Hannan, Caroline M Gorvin, et al.
Page
of 3