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Scientific Reports
|
March 31, 2026
Aminoadipate-semialdehyde synthase, a potential target for substrate reduction therapy in glutaric aciduria type 1
Celine 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 loss
Martin 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 mice
Sabine 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 mouse
Caroline 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 mutation
Sibylle 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 aciduria
Marie 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 risk
Claudia 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 phenotypes
Robert 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 data
Viola 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) disease
Howard T Jacobs, Marten Szibor, Birgit Rathkolb, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 75) with videos related to
Sort By:
Page
of 8
Scientific Reports
|
March 31, 2026
Aminoadipate-semialdehyde synthase, a potential target for substrate reduction therapy in glutaric aciduria type 1
Celine 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 loss
Martin 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 mice
Sabine 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 mouse
Caroline 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 mutation
Sibylle 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 aciduria
Marie 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 risk
Claudia 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 phenotypes
Robert 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 data
Viola 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) disease
Howard T Jacobs, Marten Szibor, Birgit Rathkolb, et al.
Page
of 8