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The Journal of Clinical Investigation
|
September 21, 2021
Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model
Eva Auffenberg, Ulrike Bs Hedrich, Raffaella Barbieri, et al.
Iscience
|
October 27, 2025
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism
Jean-Pierre Gillet, Louise Gerard, Wilfred Vieira, et al.
Endocrinology
|
June 18, 2024
Comparative Phenotyping of Mice Reveals Canonical and Noncanonical Physiological Functions of TRα and TRβ
Georg Sebastian Hönes, Daniela Geist, Christina Wenzek, et al.
Disease Models & Mechanisms
|
December 29, 2021
Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk
Lillian Garrett, Patricia Da Silva-Buttkus, Birgit Rathkolb, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 9, 2023
Knockout mouse models as a resource for the study of rare diseases
Patricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald, 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.
JACC. Basic to Translational Science
|
June 13, 2026
Targeting Inflammation by Pioglitazone and its R-Enantiomer Mitigates Pathological Myocardial Remodeling in Murine Hypertrophic Cardiomyopathy
Anna-Theresa Pfaller, Claudia Veneziano, Sarala Raj Murthi, 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.
Nature Communications
|
December 5, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes
Tim P Hasenbein, Sarah Hoelzl, Zachary D Smith, et al.
Scientific Reports
|
January 17, 2025
Contribution of hypoxia-inducible factor 1alpha to pathogenesis of sarcomeric hypertrophic cardiomyopathy
Sarala Raj Murthi, Andreas Petry, Bachuki Shashikadze, et al.
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Search research articles
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Showing results (21-30 of 41) with videos related to
Sort By:
Page
of 5
The Journal of Clinical Investigation
|
September 21, 2021
Hyperexcitable interneurons trigger cortical spreading depression in an Scn1a migraine model
Eva Auffenberg, Ulrike Bs Hedrich, Raffaella Barbieri, et al.
Iscience
|
October 27, 2025
Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolism
Jean-Pierre Gillet, Louise Gerard, Wilfred Vieira, et al.
Endocrinology
|
June 18, 2024
Comparative Phenotyping of Mice Reveals Canonical and Noncanonical Physiological Functions of TRα and TRβ
Georg Sebastian Hönes, Daniela Geist, Christina Wenzek, et al.
Disease Models & Mechanisms
|
December 29, 2021
Post-synaptic scaffold protein TANC2 in psychiatric and somatic disease risk
Lillian Garrett, Patricia Da Silva-Buttkus, Birgit Rathkolb, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
May 9, 2023
Knockout mouse models as a resource for the study of rare diseases
Patricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald, 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.
JACC. Basic to Translational Science
|
June 13, 2026
Targeting Inflammation by Pioglitazone and its R-Enantiomer Mitigates Pathological Myocardial Remodeling in Murine Hypertrophic Cardiomyopathy
Anna-Theresa Pfaller, Claudia Veneziano, Sarala Raj Murthi, 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.
Nature Communications
|
December 5, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes
Tim P Hasenbein, Sarah Hoelzl, Zachary D Smith, et al.
Scientific Reports
|
January 17, 2025
Contribution of hypoxia-inducible factor 1alpha to pathogenesis of sarcomeric hypertrophic cardiomyopathy
Sarala Raj Murthi, Andreas Petry, Bachuki Shashikadze, et al.
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of 5