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

Ingo Kurth

Showing results (1-10 of 145) with videos related to

Pageof 15
Sort By:
The International Journal of Biochemistry & Cell Biology|July 7, 2020
Long-read sequencing to understand genome biology and cell functionFlorian Kraft, Ingo Kurth
Brain : a Journal of Neurology|October 5, 2014
Membrane-shaping disorders: a common pathway in axon degenerationChristian A Hübner, Ingo Kurth
Cellular and Molecular Life Sciences : CMLS|January 23, 2019
A disease causing ATLASTIN 3 mutation affects multiple endoplasmic reticulum-related pathwaysLaura Behrendt, Ingo Kurth, Christoph Kaether
Neuro-Ophthalmology (Aeolus Press)|November 20, 2019
A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV)Beena Suresh, Vaishnavi Reddy, Ingo Kurth, et al.
European Journal of Medical Genetics|May 18, 2019
Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variationsThomas Eggermann, Matthias Begemann, Ingo Kurth, et al.
Journal of Neurology|August 10, 2022
Novel phenotype with prominent cerebellar oculomotor dysfunction in spastic paraplegia type 39Sebastian Viertauer, Ingo Kurth, Katja Eggermann, et al.
Der Internist|December 20, 2018
[Neuropathic pain syndromes and channelopathies]Maike F Dohrn, Angelika Lampert, Nurcan Üçeyler, et al.
The Journal of Biological Chemistry|September 7, 2006
Germ cell nuclear factor is a repressor of CRIPTO-1 and CRIPTO-3Moritz Hentschke, Ingo Kurth, Uwe Borgmeyer, et al.
BMC Nephrology|October 22, 2018
No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuriaKathrin Olschok, Udo Vester, Sven Lahme, et al.
Translational Neurodegeneration|December 31, 2016
Stroke-like onset of brain stem degeneration presents with unique MRI sign and heterozygous <i>NMNAT2</i> variant: a case reportAlexander Schulz, Franziska Wagner, Martin Ungelenk, et al.
Pageof 15

Showing results (1-10 of 145) with videos related to

Sort By:
Pageof 15
The International Journal of Biochemistry & Cell Biology|July 7, 2020
Long-read sequencing to understand genome biology and cell functionFlorian Kraft, Ingo Kurth
Brain : a Journal of Neurology|October 5, 2014
Membrane-shaping disorders: a common pathway in axon degenerationChristian A Hübner, Ingo Kurth
Cellular and Molecular Life Sciences : CMLS|January 23, 2019
A disease causing ATLASTIN 3 mutation affects multiple endoplasmic reticulum-related pathwaysLaura Behrendt, Ingo Kurth, Christoph Kaether
Neuro-Ophthalmology (Aeolus Press)|November 20, 2019
A Child Presenting with Recurrent Corneal Ulcers: Hereditary Sensory and Autonomic Neuropathy IV (HSAN IV)Beena Suresh, Vaishnavi Reddy, Ingo Kurth, et al.
European Journal of Medical Genetics|May 18, 2019
Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variationsThomas Eggermann, Matthias Begemann, Ingo Kurth, et al.
Journal of Neurology|August 10, 2022
Novel phenotype with prominent cerebellar oculomotor dysfunction in spastic paraplegia type 39Sebastian Viertauer, Ingo Kurth, Katja Eggermann, et al.
Der Internist|December 20, 2018
[Neuropathic pain syndromes and channelopathies]Maike F Dohrn, Angelika Lampert, Nurcan Üçeyler, et al.
The Journal of Biological Chemistry|September 7, 2006
Germ cell nuclear factor is a repressor of CRIPTO-1 and CRIPTO-3Moritz Hentschke, Ingo Kurth, Uwe Borgmeyer, et al.
BMC Nephrology|October 22, 2018
No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuriaKathrin Olschok, Udo Vester, Sven Lahme, et al.
Translational Neurodegeneration|December 31, 2016
Stroke-like onset of brain stem degeneration presents with unique MRI sign and heterozygous <i>NMNAT2</i> variant: a case reportAlexander Schulz, Franziska Wagner, Martin Ungelenk, et al.
Pageof 15