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Helmut Fuchs

Showing results (181-190 of 272) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 9, 2023
Knockout mouse models as a resource for the study of rare diseasesPatricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald, et al.
Plos One|March 23, 2016
Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant MiceSudhir Kumar, Birgit Rathkolb, Elisabeth Kemter, et al.
The EMBO Journal|August 9, 2018
RNA editing of Filamin A pre-mRNA regulates vascular contraction and diastolic blood pressureMamta Jain, Tomer D Mann, Maja Stulić, et al.
Journal of Cell Science|March 17, 2011
Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epitheliaJuha Saarikangas, Pieta K Mattila, Markku Varjosalo, et al.
The EMBO Journal|July 27, 2014
Aberrant methylation of tRNAs links cellular stress to neuro-developmental disordersSandra Blanco, Sabine Dietmann, Joana V Flores, et al.
Arthritis and Rheumatism|February 10, 2011
A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine modelKoichiro Abe, Helmut Fuchs, Auke Boersma, 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.
Molecular and Cellular Biology|March 2, 2006
Generation and characterization of dickkopf3 mutant miceIvan del Barco Barrantes, Ana Montero-Pedrazuela, Ana Guadaño-Ferraz, 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.
Translational Psychiatry|January 22, 2019
Cognitive impairment and autistic-like behaviour in SAPAP4-deficient miceClaudia Schob, Fabio Morellini, Ora Ohana, et al.
Pageof 28

Showing results (181-190 of 272) with videos related to

Sort By:
Pageof 28
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 9, 2023
Knockout mouse models as a resource for the study of rare diseasesPatricia da Silva-Buttkus, Nadine Spielmann, Tanja Klein-Rodewald, et al.
Plos One|March 23, 2016
Generation and Standardized, Systemic Phenotypic Analysis of Pou3f3L423P Mutant MiceSudhir Kumar, Birgit Rathkolb, Elisabeth Kemter, et al.
The EMBO Journal|August 9, 2018
RNA editing of Filamin A pre-mRNA regulates vascular contraction and diastolic blood pressureMamta Jain, Tomer D Mann, Maja Stulić, et al.
Journal of Cell Science|March 17, 2011
Missing-in-metastasis MIM/MTSS1 promotes actin assembly at intercellular junctions and is required for integrity of kidney epitheliaJuha Saarikangas, Pieta K Mattila, Markku Varjosalo, et al.
The EMBO Journal|July 27, 2014
Aberrant methylation of tRNAs links cellular stress to neuro-developmental disordersSandra Blanco, Sabine Dietmann, Joana V Flores, et al.
Arthritis and Rheumatism|February 10, 2011
A novel N-ethyl-N-nitrosourea-induced mutation in phospholipase Cγ2 causes inflammatory arthritis, metabolic defects, and male infertility in vitro in a murine modelKoichiro Abe, Helmut Fuchs, Auke Boersma, 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.
Molecular and Cellular Biology|March 2, 2006
Generation and characterization of dickkopf3 mutant miceIvan del Barco Barrantes, Ana Montero-Pedrazuela, Ana Guadaño-Ferraz, 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.
Translational Psychiatry|January 22, 2019
Cognitive impairment and autistic-like behaviour in SAPAP4-deficient miceClaudia Schob, Fabio Morellini, Ora Ohana, et al.
Pageof 28