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

Verena Peters

Showing results (41-50 of 72) with videos related to

Pageof 8
Sort By:
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 14, 2017
Methylglyoxal and Advanced Glycation End Products in Patients with Diabetes - What We Know so Far and the Missing LinksJan Benedikt Groener, Dimitrios Oikonomou, Ruan Cheko, et al.
International Journal of Molecular Sciences|September 16, 2018
Protective Actions of Anserine Under Diabetic ConditionsVerena Peters, Vittorio Calabrese, Elisabete Forsberg, et al.
Journal of Inherited Metabolic Disease|August 21, 2023
Kidney urinary biomarkers in patients with branched-chain amino acid and cobalamin metabolism defectsFelix Köpfer, Sven F Garbade, Kristina Klingbeil, et al.
Environmental Microbiology|May 28, 2015
A novel protein quality control mechanism contributes to heat shock resistance of worldwide-distributed Pseudomonas aeruginosa clone C strainsChanghan Lee, Edvard Wigren, Janja Trček, et al.
Human Mutation|March 26, 2003
Mutations in the AUH gene cause 3-methylglutaconic aciduria type IT B Nga Ly, Verena Peters, K Michael Gibson, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 10, 2016
A scavenger peptide prevents methylglyoxal induced pain in miceSebastian Brings, Thomas Fleming, Svenja De Buhr, et al.
The Journal of Clinical Investigation|March 20, 2002
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IIdBengt Hansske, Christian Thiel, Torben Lübke, et al.
Antioxidants (Basel, Switzerland)|December 23, 2020
Hydrogen Sulfide and Carnosine: Modulation of Oxidative Stress and Inflammation in Kidney and Brain AxisVittorio Calabrese, Maria Scuto, Angela Trovato Salinaro, et al.
Amino Acids|July 25, 2015
Intrinsic carnosine metabolism in the human kidneyVerena Peters, Celine Q F Klessens, Hans J Baelde, et al.
Molecular Genetics and Metabolism Reports|November 19, 2020
Fatal outcome after heart surgery in PMM2-CDG due to a rare homozygous gene variant with double effectsMarlen Görlacher, Eleftheria Panagiotou, Nastassja Himmelreich, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|April 14, 2017
Methylglyoxal and Advanced Glycation End Products in Patients with Diabetes - What We Know so Far and the Missing LinksJan Benedikt Groener, Dimitrios Oikonomou, Ruan Cheko, et al.
International Journal of Molecular Sciences|September 16, 2018
Protective Actions of Anserine Under Diabetic ConditionsVerena Peters, Vittorio Calabrese, Elisabete Forsberg, et al.
Journal of Inherited Metabolic Disease|August 21, 2023
Kidney urinary biomarkers in patients with branched-chain amino acid and cobalamin metabolism defectsFelix Köpfer, Sven F Garbade, Kristina Klingbeil, et al.
Environmental Microbiology|May 28, 2015
A novel protein quality control mechanism contributes to heat shock resistance of worldwide-distributed Pseudomonas aeruginosa clone C strainsChanghan Lee, Edvard Wigren, Janja Trček, et al.
Human Mutation|March 26, 2003
Mutations in the AUH gene cause 3-methylglutaconic aciduria type IT B Nga Ly, Verena Peters, K Michael Gibson, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|December 10, 2016
A scavenger peptide prevents methylglyoxal induced pain in miceSebastian Brings, Thomas Fleming, Svenja De Buhr, et al.
The Journal of Clinical Investigation|March 20, 2002
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IIdBengt Hansske, Christian Thiel, Torben Lübke, et al.
Antioxidants (Basel, Switzerland)|December 23, 2020
Hydrogen Sulfide and Carnosine: Modulation of Oxidative Stress and Inflammation in Kidney and Brain AxisVittorio Calabrese, Maria Scuto, Angela Trovato Salinaro, et al.
Amino Acids|July 25, 2015
Intrinsic carnosine metabolism in the human kidneyVerena Peters, Celine Q F Klessens, Hans J Baelde, et al.
Molecular Genetics and Metabolism Reports|November 19, 2020
Fatal outcome after heart surgery in PMM2-CDG due to a rare homozygous gene variant with double effectsMarlen Görlacher, Eleftheria Panagiotou, Nastassja Himmelreich, et al.
Pageof 8