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Julia Calzada-Wack

Showing results (41-50 of 70) with videos related to

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Translational Psychiatry|January 22, 2019
Cognitive impairment and autistic-like behaviour in SAPAP4-deficient miceClaudia Schob, Fabio Morellini, Ora Ohana, et al.
Science Advances|April 11, 2025
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenitaAdrián Sanz-Moreno, Lore Becker, Kan Xie, et al.
Plos One|December 16, 2014
MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathyLore Becker, Eva Kling, Evelyn Schiller, 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.
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.
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.
Nature Methods|June 16, 2022
Mass spectrometry-based draft of the mouse proteomePiero Giansanti, Patroklos Samaras, Yangyang Bian, et al.
Nature Communications|December 5, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomesTim P Hasenbein, Sarah Hoelzl, Zachary D Smith, et al.
Communications Biology|May 3, 2022
Dietary intervention improves health metrics and life expectancy of the genetically obese Titan mouseAnnika Müller-Eigner, Adrián Sanz-Moreno, Irene de-Diego, et al.
Science Advances|October 24, 2025
Loss of histone macroH2A1.1 causes kidney abnormalities secondary to a change in nutrient metabolizationRené Winkler, Gemma Comas-Armangué, David Corujo, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
Translational Psychiatry|January 22, 2019
Cognitive impairment and autistic-like behaviour in SAPAP4-deficient miceClaudia Schob, Fabio Morellini, Ora Ohana, et al.
Science Advances|April 11, 2025
Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenitaAdrián Sanz-Moreno, Lore Becker, Kan Xie, et al.
Plos One|December 16, 2014
MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathyLore Becker, Eva Kling, Evelyn Schiller, 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.
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.
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.
Nature Methods|June 16, 2022
Mass spectrometry-based draft of the mouse proteomePiero Giansanti, Patroklos Samaras, Yangyang Bian, et al.
Nature Communications|December 5, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomesTim P Hasenbein, Sarah Hoelzl, Zachary D Smith, et al.
Communications Biology|May 3, 2022
Dietary intervention improves health metrics and life expectancy of the genetically obese Titan mouseAnnika Müller-Eigner, Adrián Sanz-Moreno, Irene de-Diego, et al.
Science Advances|October 24, 2025
Loss of histone macroH2A1.1 causes kidney abnormalities secondary to a change in nutrient metabolizationRené Winkler, Gemma Comas-Armangué, David Corujo, et al.
Pageof 7