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Muriel T Davisson

Showing results (21-30 of 40) with videos related to

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Genomics|March 7, 2006
Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouseDominique Simon-Chazottes, Sylvie Tutois, Michael Kuehn, et al.
Human Molecular Genetics|April 27, 2013
Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe diseaseGregory B Potter, Marta Santos, Muriel T Davisson, 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.
Investigative Ophthalmology & Visual Science|February 5, 2010
The mouse model of Down syndrome Ts65Dn presents visual deficits as assessed by pattern visual evoked potentialsJonah Jacob Scott-McKean, Bo Chang, Ronald E Hurd, 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.
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.
Academic Journal of Xian Jiaotong University : AJXJTU = Xi'An Jiao Tong Da Xue Xue Bao (Yi Wen Ban)|December 24, 2010
Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10Qing Yin Zheng, Belinda S Harris, Patricia F Ward-Bailey, et al.
Plos One|January 14, 2012
A spontaneous mutation in contactin 1 in the mouseMuriel T Davisson, Roderick T Bronson, Abigail L D Tadenev, et al.
Genomics|November 29, 2005
Chromosomal inversion discovered in C3H/HeJ miceEllen C Akeson, Leah Rae Donahue, Wesley G Beamer, et al.
Nature|August 15, 2006
Editing-defective tRNA synthetase causes protein misfolding and neurodegenerationJeong Woong Lee, Kirk Beebe, Leslie A Nangle, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Genomics|March 7, 2006
Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouseDominique Simon-Chazottes, Sylvie Tutois, Michael Kuehn, et al.
Human Molecular Genetics|April 27, 2013
Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe diseaseGregory B Potter, Marta Santos, Muriel T Davisson, 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.
Investigative Ophthalmology & Visual Science|February 5, 2010
The mouse model of Down syndrome Ts65Dn presents visual deficits as assessed by pattern visual evoked potentialsJonah Jacob Scott-McKean, Bo Chang, Ronald E Hurd, 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.
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.
Academic Journal of Xian Jiaotong University : AJXJTU = Xi'An Jiao Tong Da Xue Xue Bao (Yi Wen Ban)|December 24, 2010
Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10Qing Yin Zheng, Belinda S Harris, Patricia F Ward-Bailey, et al.
Plos One|January 14, 2012
A spontaneous mutation in contactin 1 in the mouseMuriel T Davisson, Roderick T Bronson, Abigail L D Tadenev, et al.
Genomics|November 29, 2005
Chromosomal inversion discovered in C3H/HeJ miceEllen C Akeson, Leah Rae Donahue, Wesley G Beamer, et al.
Nature|August 15, 2006
Editing-defective tRNA synthetase causes protein misfolding and neurodegenerationJeong Woong Lee, Kirk Beebe, Leslie A Nangle, et al.
Pageof 4