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Sandra Piltz

Showing results (1-10 of 16) with videos related to

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Plos Genetics|March 19, 2013
Mechanistic insight into the pathology of polyalanine expansion disorders revealed by a mouse model for X linked hypopituitarismJames Hughes, Sandra Piltz, Nicholas Rogers, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 13, 2022
Generation of Gene Drive Mice for Invasive Pest Population SuppressionMark D Bunting, Chandran Pfitzner, Luke Gierus, et al.
Plos One|November 5, 2021
The Nestin neural enhancer is essential for normal levels of endogenous Nestin in neuroprogenitors but is not required for embryo developmentElla Thomson, Ruby Dawson, Chee Ho H'ng, et al.
The CRISPR Journal|April 26, 2019
Expanding the RNA-Guided Endonuclease Toolkit for Mouse Genome EditingLouise Robertson, Daniel Pederick, Sandra Piltz, et al.
Scientific Reports|October 5, 2017
Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signallingJames Hughes, Ruby Dawson, Melinda Tea, et al.
Neurobiology of Disease|May 16, 2018
PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering EpilepsyClaire C Homan, Stephen Pederson, Thu-Hien To, et al.
Nature|August 10, 2018
Large deletions induced by Cas9 cleavageFatwa Adikusuma, Sandra Piltz, Mark A Corbett, et al.
Plos One|February 1, 2012
Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic miceKristie Lee, Jacqueline Tan, Michael B Morris, et al.
Nucleic Acids Research|September 17, 2021
Optimized nickase- and nuclease-based prime editing in human and mouse cellsFatwa Adikusuma, Caleb Lushington, Jayshen Arudkumar, et al.
Genes, Brain, and Behavior|January 8, 2020
Investigating cortical features of Sotos syndrome using mice heterozygous for Nsd1Sabrina Oishi, Oressia Zalucki, Michelle S Vega, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Plos Genetics|March 19, 2013
Mechanistic insight into the pathology of polyalanine expansion disorders revealed by a mouse model for X linked hypopituitarismJames Hughes, Sandra Piltz, Nicholas Rogers, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 13, 2022
Generation of Gene Drive Mice for Invasive Pest Population SuppressionMark D Bunting, Chandran Pfitzner, Luke Gierus, et al.
Plos One|November 5, 2021
The Nestin neural enhancer is essential for normal levels of endogenous Nestin in neuroprogenitors but is not required for embryo developmentElla Thomson, Ruby Dawson, Chee Ho H'ng, et al.
The CRISPR Journal|April 26, 2019
Expanding the RNA-Guided Endonuclease Toolkit for Mouse Genome EditingLouise Robertson, Daniel Pederick, Sandra Piltz, et al.
Scientific Reports|October 5, 2017
Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signallingJames Hughes, Ruby Dawson, Melinda Tea, et al.
Neurobiology of Disease|May 16, 2018
PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering EpilepsyClaire C Homan, Stephen Pederson, Thu-Hien To, et al.
Nature|August 10, 2018
Large deletions induced by Cas9 cleavageFatwa Adikusuma, Sandra Piltz, Mark A Corbett, et al.
Plos One|February 1, 2012
Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic miceKristie Lee, Jacqueline Tan, Michael B Morris, et al.
Nucleic Acids Research|September 17, 2021
Optimized nickase- and nuclease-based prime editing in human and mouse cellsFatwa Adikusuma, Caleb Lushington, Jayshen Arudkumar, et al.
Genes, Brain, and Behavior|January 8, 2020
Investigating cortical features of Sotos syndrome using mice heterozygous for Nsd1Sabrina Oishi, Oressia Zalucki, Michelle S Vega, et al.
Pageof 2