Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Nico Fuhrmann

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Molecular Neurodegeneration|September 27, 2013
Dominant optic atrophy, OPA1, and mitochondrial quality control: understanding mitochondrial network dynamicsMarcel V Alavi, Nico Fuhrmann
Genome|June 9, 2020
The importance of DNA barcode choice in biogeographic analyses - a case study on marine midges of the genus <i>Clunio</i>Nico Fuhrmann, Tobias S Kaiser
Elife|February 28, 2023
Polygenic adaptation from standing genetic variation allows rapid ecotype formationNico Fuhrmann, Celine Prakash, Tobias S Kaiser
Human Mutation|August 28, 2007
Comprehensive cDNA study and quantitative transcript analysis of mutant OPA1 transcripts containing premature termination codonsSimone Schimpf, Nico Fuhrmann, Simone Schaich, et al.
Investigative Ophthalmology & Visual Science|October 17, 2009
Electrophysiological and histologic assessment of retinal ganglion cell fate in a mouse model for OPA1-associated autosomal dominant optic atrophyPeter Heiduschka, Sven Schnichels, Nico Fuhrmann, et al.
Genome Biology and Evolution|July 17, 2024
Chromosome-Level Genome Assembly of the Viviparous Eelpout Zoarces viviparusNico Fuhrmann, Marie V Brasseur, Christina E Bakowski, et al.
Experimental Neurology|October 10, 2009
Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophyMarcel V Alavi, Nico Fuhrmann, Huu Phuc Nguyen, et al.
Molecular Neurodegeneration|June 16, 2010
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophyNico Fuhrmann, Simone Schimpf, York Kamenisch, et al.
Toxins|January 6, 2018
A Dipteran's Novel Sucker Punch: Evolution of Arthropod Atypical Venom with a Neurotoxic Component in Robber Flies (Asilidae, Diptera)Stephan Holger Drukewitz, Nico Fuhrmann, Eivind A B Undheim, et al.
Clinical Genetics|December 5, 2024
Biallelic Variants in LRRC45 Impair Ciliogenesis and Cause a Severe Neurological DisorderPeriyasamy Radhakrishnan, Neha Quadri, Florian Erger, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Molecular Neurodegeneration|September 27, 2013
Dominant optic atrophy, OPA1, and mitochondrial quality control: understanding mitochondrial network dynamicsMarcel V Alavi, Nico Fuhrmann
Genome|June 9, 2020
The importance of DNA barcode choice in biogeographic analyses - a case study on marine midges of the genus <i>Clunio</i>Nico Fuhrmann, Tobias S Kaiser
Elife|February 28, 2023
Polygenic adaptation from standing genetic variation allows rapid ecotype formationNico Fuhrmann, Celine Prakash, Tobias S Kaiser
Human Mutation|August 28, 2007
Comprehensive cDNA study and quantitative transcript analysis of mutant OPA1 transcripts containing premature termination codonsSimone Schimpf, Nico Fuhrmann, Simone Schaich, et al.
Investigative Ophthalmology & Visual Science|October 17, 2009
Electrophysiological and histologic assessment of retinal ganglion cell fate in a mouse model for OPA1-associated autosomal dominant optic atrophyPeter Heiduschka, Sven Schnichels, Nico Fuhrmann, et al.
Genome Biology and Evolution|July 17, 2024
Chromosome-Level Genome Assembly of the Viviparous Eelpout Zoarces viviparusNico Fuhrmann, Marie V Brasseur, Christina E Bakowski, et al.
Experimental Neurology|October 10, 2009
Subtle neurological and metabolic abnormalities in an Opa1 mouse model of autosomal dominant optic atrophyMarcel V Alavi, Nico Fuhrmann, Huu Phuc Nguyen, et al.
Molecular Neurodegeneration|June 16, 2010
Solving a 50 year mystery of a missing OPA1 mutation: more insights from the first family diagnosed with autosomal dominant optic atrophyNico Fuhrmann, Simone Schimpf, York Kamenisch, et al.
Toxins|January 6, 2018
A Dipteran's Novel Sucker Punch: Evolution of Arthropod Atypical Venom with a Neurotoxic Component in Robber Flies (Asilidae, Diptera)Stephan Holger Drukewitz, Nico Fuhrmann, Eivind A B Undheim, et al.
Clinical Genetics|December 5, 2024
Biallelic Variants in LRRC45 Impair Ciliogenesis and Cause a Severe Neurological DisorderPeriyasamy Radhakrishnan, Neha Quadri, Florian Erger, et al.
Pageof 2