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Helmut Fuchs

Showing results (71-80 of 272) with videos related to

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Experimental Eye Research|April 17, 2019
Mutation in the mouse histone gene Hist2h3c1 leads to degeneration of the lens vesicle and severe microphthalmiaSharmilee Vetrivel, Natascia Tiso, Andrea Kügler, et al.
Translational Psychiatry|February 19, 2020
A truncating Aspm allele leads to a complex cognitive phenotype and region-specific reductions in parvalbuminergic neuronsLillian Garrett, Yoon Jeung Chang, Kristina M Niedermeier, et al.
Redox Biology|October 1, 2022
Seizures, ataxia and parvalbumin-expressing interneurons respond to selenium supply in Selenop-deficient miceUlrich Schweizer, Eva K Wirth, Thomas Klopstock, et al.
The Journal of Biological Chemistry|June 18, 2009
Characterization of phospholipase C gamma enzymes with gain-of-function mutationsKaty L Everett, Tom D Bunney, Youngdae Yoon, et al.
Plos One|June 2, 2017
Improved efficacy of allergen-specific immunotherapy by JAK inhibition in a murine model of allergic asthmaAntonio Aguilar-Pimentel, Anke Graessel, Francesca Alessandrini, et al.
Developmental and Comparative Immunology|July 27, 2017
High levels of eukaryotic Initiation Factor 6 (eIF6) are required for immune system homeostasis and for steering the glycolytic flux of TCR-stimulated CD4<sup>+</sup> T cells in both mice and humansNicola Manfrini, Sara Ricciardi, Annarita Miluzio, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 16, 2023
A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in miceJiri Lindovsky, Zuzana Nichtova, Nathalia R V Dragano, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2019
Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humansKoichiro Abe, Allison Cox, Nobuhiko Takamatsu, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promotersJochen Graw, Jana Löster, Oliver Puk, et al.
Plos Genetics|November 1, 2008
The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing lossSarah L Spiden, Mario Bortolozzi, Francesca Di Leva, et al.
Pageof 28

Showing results (71-80 of 272) with videos related to

Sort By:
Pageof 28
Experimental Eye Research|April 17, 2019
Mutation in the mouse histone gene Hist2h3c1 leads to degeneration of the lens vesicle and severe microphthalmiaSharmilee Vetrivel, Natascia Tiso, Andrea Kügler, et al.
Translational Psychiatry|February 19, 2020
A truncating Aspm allele leads to a complex cognitive phenotype and region-specific reductions in parvalbuminergic neuronsLillian Garrett, Yoon Jeung Chang, Kristina M Niedermeier, et al.
Redox Biology|October 1, 2022
Seizures, ataxia and parvalbumin-expressing interneurons respond to selenium supply in Selenop-deficient miceUlrich Schweizer, Eva K Wirth, Thomas Klopstock, et al.
The Journal of Biological Chemistry|June 18, 2009
Characterization of phospholipase C gamma enzymes with gain-of-function mutationsKaty L Everett, Tom D Bunney, Youngdae Yoon, et al.
Plos One|June 2, 2017
Improved efficacy of allergen-specific immunotherapy by JAK inhibition in a murine model of allergic asthmaAntonio Aguilar-Pimentel, Anke Graessel, Francesca Alessandrini, et al.
Developmental and Comparative Immunology|July 27, 2017
High levels of eukaryotic Initiation Factor 6 (eIF6) are required for immune system homeostasis and for steering the glycolytic flux of TCR-stimulated CD4<sup>+</sup> T cells in both mice and humansNicola Manfrini, Sara Ricciardi, Annarita Miluzio, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 16, 2023
A review of standardized high-throughput cardiovascular phenotyping with a link to metabolism in miceJiri Lindovsky, Zuzana Nichtova, Nathalia R V Dragano, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2019
Gain-of-function mutations in a member of the Src family kinases cause autoinflammatory bone disease in mice and humansKoichiro Abe, Allison Cox, Nobuhiko Takamatsu, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promotersJochen Graw, Jana Löster, Oliver Puk, et al.
Plos Genetics|November 1, 2008
The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing lossSarah L Spiden, Mario Bortolozzi, Francesca Di Leva, et al.
Pageof 28