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Helmut Fuchs

Showing results (21-30 of 272) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 13, 2002
V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in miceJochen Graw, Jana Löster, Dian Soewarto, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 5, 2006
Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71rco12 and Krt71rco13Fabian Runkel, Matthias Klaften, Kerstin Koch, et al.
Experimental Eye Research|November 22, 2019
Spectral domain - Optical coherence tomography (SD-OCT) as a monitoring tool for alterations in mouse lensesDaniel Pawliczek, Claudia Dalke, Helmut Fuchs, et al.
Human Molecular Genetics|June 5, 2014
Peroxidasin is essential for eye development in the mouseXiaohe Yan, Sibylle Sabrautzki, Marion Horsch, et al.
Current Protocols in Mouse Biology|March 3, 2015
Glucose tolerance tests for systematic screening of glucose homeostasis in miceJan Rozman, Birgit Rathkolb, Susanne Neschen, et al.
Genetics|May 2, 2006
Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36Yoshihiro Noguchi, Kiyoto Kurima, Tomoko Makishima, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 20, 2022
A rationale for considering heart/brain axis control in neuropsychiatric diseaseLillian Garrett, Dietrich Trümbach, Nadine Spielmann, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 25, 2004
A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairmentCharlotte R Rhodes, Ronna Hertzano, Helmut Fuchs, et al.
Journal of Comparative Physiology. B, Biochemical, Systemic, and Environmental Physiology|May 3, 2014
High-throughput phenotypic assessment of cardiac physiology in four commonly used inbred mouse strainsKristin Moreth, Ralf Fischer, Helmut Fuchs, et al.
Molecular Neurobiology|October 7, 2018
Crybb2 Mutations Consistently Affect Schizophrenia Endophenotypes in MiceTamara Heermann, Lillian Garrett, Wolfgang Wurst, et al.
Pageof 28

Showing results (21-30 of 272) with videos related to

Sort By:
Pageof 28
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 13, 2002
V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in miceJochen Graw, Jana Löster, Dian Soewarto, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 5, 2006
Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71rco12 and Krt71rco13Fabian Runkel, Matthias Klaften, Kerstin Koch, et al.
Experimental Eye Research|November 22, 2019
Spectral domain - Optical coherence tomography (SD-OCT) as a monitoring tool for alterations in mouse lensesDaniel Pawliczek, Claudia Dalke, Helmut Fuchs, et al.
Human Molecular Genetics|June 5, 2014
Peroxidasin is essential for eye development in the mouseXiaohe Yan, Sibylle Sabrautzki, Marion Horsch, et al.
Current Protocols in Mouse Biology|March 3, 2015
Glucose tolerance tests for systematic screening of glucose homeostasis in miceJan Rozman, Birgit Rathkolb, Susanne Neschen, et al.
Genetics|May 2, 2006
Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (Tmc1Bth) mouse model of progressive hearing loss DFNA36Yoshihiro Noguchi, Kiyoto Kurima, Tomoko Makishima, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 20, 2022
A rationale for considering heart/brain axis control in neuropsychiatric diseaseLillian Garrett, Dietrich Trümbach, Nadine Spielmann, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 25, 2004
A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairmentCharlotte R Rhodes, Ronna Hertzano, Helmut Fuchs, et al.
Journal of Comparative Physiology. B, Biochemical, Systemic, and Environmental Physiology|May 3, 2014
High-throughput phenotypic assessment of cardiac physiology in four commonly used inbred mouse strainsKristin Moreth, Ralf Fischer, Helmut Fuchs, et al.
Molecular Neurobiology|October 7, 2018
Crybb2 Mutations Consistently Affect Schizophrenia Endophenotypes in MiceTamara Heermann, Lillian Garrett, Wolfgang Wurst, et al.
Pageof 28