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

Guenter Schwarz

Showing results (51-60 of 73) with videos related to

Pageof 8
Sort By:
Human Genetics|May 4, 2016
Mouse model for molybdenum cofactor deficiency type B recapitulates the phenotype observed in molybdenum cofactor deficient patientsJoanna Jakubiczka-Smorag, Jose Angel Santamaria-Araujo, Imke Metz, et al.
The Journal of Biological Chemistry|July 29, 2006
Function and structure of the molybdenum cofactor carrier protein from Chlamydomonas reinhardtiiKatrin Fischer, Angel Llamas, Manuel Tejada-Jimenez, et al.
Frontiers in Cardiovascular Medicine|October 20, 2022
Sodium thiosulfate, a source of hydrogen sulfide, stimulates endothelial cell proliferation and neovascularizationDiane Macabrey, Jaroslava Joniová, Quentin Gasser, et al.
Plos One|January 28, 2014
Low-molecular weight heparin increases circulating sFlt-1 levels and enhances urinary eliminationHenning Hagmann, Verena Bossung, Abdel Ali Belaidi, et al.
Journal of Inherited Metabolic Disease|November 6, 2021
A defect in molybdenum cofactor binding causes an attenuated form of sulfite oxidase deficiencyAlexander Tobias Kaczmarek, Daniel Bender, Titus Gehling, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 25, 2017
Molybdenum cofactor deficiency type A: Prenatal monitoring using MRICharlotte M A Lubout, Terry G J Derks, Linda Meiners, et al.
Journal of Inherited Metabolic Disease|April 17, 2024
Consensus guidelines for the diagnosis and management of isolated sulfite oxidase deficiency and molybdenum cofactor deficienciesBernd C Schwahn, Francjan van Spronsen, Albert Misko, et al.
Pediatrics|April 14, 2010
Successful treatment of molybdenum cofactor deficiency type A with cPMPAlex Veldman, José Angel Santamaria-Araujo, Silvio Sollazzo, et al.
European Journal of Pediatrics|July 24, 2025
A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiencySung Kweon Cho, Guenter Schwarz, Velibor Tasic, et al.
The Journal of Clinical Investigation|November 7, 2017
S-sulfocysteine/NMDA receptor-dependent signaling underlies neurodegeneration in molybdenum cofactor deficiencyAvadh Kumar, Borislav Dejanovic, Florian Hetsch, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
Human Genetics|May 4, 2016
Mouse model for molybdenum cofactor deficiency type B recapitulates the phenotype observed in molybdenum cofactor deficient patientsJoanna Jakubiczka-Smorag, Jose Angel Santamaria-Araujo, Imke Metz, et al.
The Journal of Biological Chemistry|July 29, 2006
Function and structure of the molybdenum cofactor carrier protein from Chlamydomonas reinhardtiiKatrin Fischer, Angel Llamas, Manuel Tejada-Jimenez, et al.
Frontiers in Cardiovascular Medicine|October 20, 2022
Sodium thiosulfate, a source of hydrogen sulfide, stimulates endothelial cell proliferation and neovascularizationDiane Macabrey, Jaroslava Joniová, Quentin Gasser, et al.
Plos One|January 28, 2014
Low-molecular weight heparin increases circulating sFlt-1 levels and enhances urinary eliminationHenning Hagmann, Verena Bossung, Abdel Ali Belaidi, et al.
Journal of Inherited Metabolic Disease|November 6, 2021
A defect in molybdenum cofactor binding causes an attenuated form of sulfite oxidase deficiencyAlexander Tobias Kaczmarek, Daniel Bender, Titus Gehling, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 25, 2017
Molybdenum cofactor deficiency type A: Prenatal monitoring using MRICharlotte M A Lubout, Terry G J Derks, Linda Meiners, et al.
Journal of Inherited Metabolic Disease|April 17, 2024
Consensus guidelines for the diagnosis and management of isolated sulfite oxidase deficiency and molybdenum cofactor deficienciesBernd C Schwahn, Francjan van Spronsen, Albert Misko, et al.
Pediatrics|April 14, 2010
Successful treatment of molybdenum cofactor deficiency type A with cPMPAlex Veldman, José Angel Santamaria-Araujo, Silvio Sollazzo, et al.
European Journal of Pediatrics|July 24, 2025
A prevalent MOCS2 variant in the Roma population is associated with a novel mild form of molybdenum cofactor deficiencySung Kweon Cho, Guenter Schwarz, Velibor Tasic, et al.
The Journal of Clinical Investigation|November 7, 2017
S-sulfocysteine/NMDA receptor-dependent signaling underlies neurodegeneration in molybdenum cofactor deficiencyAvadh Kumar, Borislav Dejanovic, Florian Hetsch, et al.
Pageof 8