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Lillian Garrett

Showing results (41-50 of 75) with videos related to

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Scientific Reports|March 31, 2026
Aminoadipate-semialdehyde synthase, a potential target for substrate reduction therapy in glutaric aciduria type 1Celine Saad, Sabine Jung-Klawitter, Bianca Dimitrov, et al.
Acta Neuropathologica|April 15, 2017
Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron lossMartin H Schludi, Lore Becker, Lillian Garrett, et al.
Plos One|November 27, 2013
A broad phenotypic screen identifies novel phenotypes driven by a single mutant allele in Huntington's disease CAG knock-in miceSabine M Hölter, Mary Stromberg, Marina Kovalenko, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 27, 2021
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouseCaroline A Biagosch, Silvia Vidali, Michael Faerberboeck, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 28, 2016
Viable Ednra <sup>Y129F</sup> mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutationSibylle Sabrautzki, Michael A Sandholzer, Bettina Lorenz-Depiereux, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|November 27, 2019
In-depth phenotyping reveals common and novel disease symptoms in a hemizygous knock-in mouse model (Mut-ko/ki) of mut-type methylmalonic aciduriaMarie Lucienne, Juan Antonio Aguilar-Pimentel, Oana V Amarie, et al.
Radiation and Environmental Biophysics|January 13, 2018
Lifetime study in mice after acute low-dose ionizing radiation: a multifactorial study with special focus on cataract riskClaudia Dalke, Frauke Neff, Savneet Kaur Bains, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 24, 2012
Srgap3⁻/⁻ mice present a neurodevelopmental disorder with schizophrenia-related intermediate phenotypesRobert Waltereit, Uwe Leimer, Oliver von Bohlen Und Halbach, et al.
Plos Biology|April 17, 2018
Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising dataViola André, Christine Gau, Angelika Scheideler, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 25, 2023
AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) diseaseHoward T Jacobs, Marten Szibor, Birgit Rathkolb, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Scientific Reports|March 31, 2026
Aminoadipate-semialdehyde synthase, a potential target for substrate reduction therapy in glutaric aciduria type 1Celine Saad, Sabine Jung-Klawitter, Bianca Dimitrov, et al.
Acta Neuropathologica|April 15, 2017
Spinal poly-GA inclusions in a C9orf72 mouse model trigger motor deficits and inflammation without neuron lossMartin H Schludi, Lore Becker, Lillian Garrett, et al.
Plos One|November 27, 2013
A broad phenotypic screen identifies novel phenotypes driven by a single mutant allele in Huntington's disease CAG knock-in miceSabine M Hölter, Mary Stromberg, Marina Kovalenko, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 27, 2021
A comprehensive phenotypic characterization of a whole-body Wdr45 knock-out mouseCaroline A Biagosch, Silvia Vidali, Michael Faerberboeck, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 28, 2016
Viable Ednra <sup>Y129F</sup> mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutationSibylle Sabrautzki, Michael A Sandholzer, Bettina Lorenz-Depiereux, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|November 27, 2019
In-depth phenotyping reveals common and novel disease symptoms in a hemizygous knock-in mouse model (Mut-ko/ki) of mut-type methylmalonic aciduriaMarie Lucienne, Juan Antonio Aguilar-Pimentel, Oana V Amarie, et al.
Radiation and Environmental Biophysics|January 13, 2018
Lifetime study in mice after acute low-dose ionizing radiation: a multifactorial study with special focus on cataract riskClaudia Dalke, Frauke Neff, Savneet Kaur Bains, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 24, 2012
Srgap3⁻/⁻ mice present a neurodevelopmental disorder with schizophrenia-related intermediate phenotypesRobert Waltereit, Uwe Leimer, Oliver von Bohlen Und Halbach, et al.
Plos Biology|April 17, 2018
Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising dataViola André, Christine Gau, Angelika Scheideler, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|May 25, 2023
AOX delays the onset of the lethal phenotype in a mouse model of Uqcrh (complex III) diseaseHoward T Jacobs, Marten Szibor, Birgit Rathkolb, et al.
Pageof 8