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Susan A Cook

Showing results (1-10 of 8) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 21, 2015
Loss of Clcc1 results in ER stress, misfolded protein accumulation, and neurodegenerationYichang Jia, Thomas J Jucius, Susan A Cook, et al.
Investigative Ophthalmology & Visual Science|January 17, 2012
Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesisGayle B Collin, Jungyeon Won, Wanda L Hicks, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 21, 2005
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) miceChantal M Longo-Guess, Leona H Gagnon, Susan A Cook, et al.
Kidney International|February 14, 2014
A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimersRon Korstanje, Christina R Caputo, Rosalinda A Doty, et al.
American Journal of Physiology. Renal Physiology|April 3, 2015
Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosisMuriel T Davisson, Susan A Cook, Ellen C Akeson, et al.
Journal of the American Society of Nephrology : JASN|February 13, 2009
A mouse model for Meckel syndrome type 3Susan A Cook, Gayle B Collin, Roderick T Bronson, et al.
Nature|August 15, 2006
Editing-defective tRNA synthetase causes protein misfolding and neurodegenerationJeong Woong Lee, Kirk Beebe, Leslie A Nangle, et al.
Genomics|February 8, 2003
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5Kenneth R Johnson, Priscilla W Lane, Susan A Cook, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 21, 2015
Loss of Clcc1 results in ER stress, misfolded protein accumulation, and neurodegenerationYichang Jia, Thomas J Jucius, Susan A Cook, et al.
Investigative Ophthalmology & Visual Science|January 17, 2012
Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesisGayle B Collin, Jungyeon Won, Wanda L Hicks, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 21, 2005
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) miceChantal M Longo-Guess, Leona H Gagnon, Susan A Cook, et al.
Kidney International|February 14, 2014
A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimersRon Korstanje, Christina R Caputo, Rosalinda A Doty, et al.
American Journal of Physiology. Renal Physiology|April 3, 2015
Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosisMuriel T Davisson, Susan A Cook, Ellen C Akeson, et al.
Journal of the American Society of Nephrology : JASN|February 13, 2009
A mouse model for Meckel syndrome type 3Susan A Cook, Gayle B Collin, Roderick T Bronson, et al.
Nature|August 15, 2006
Editing-defective tRNA synthetase causes protein misfolding and neurodegenerationJeong Woong Lee, Kirk Beebe, Leslie A Nangle, et al.
Genomics|February 8, 2003
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5Kenneth R Johnson, Priscilla W Lane, Susan A Cook, et al.
Pageof 1