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

V Winter

Showing results (51-60 of 85) with videos related to

Pageof 9
Sort By:
Infection and Immunity|July 19, 2000
Cloning of genes of nontypeable Haemophilus influenzae involved in penetration between human lung epithelial cellsM van Schilfgaarde, P van Ulsen, W van Der Steeg, et al.
Human Heredity|November 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern EuropeN Gregersen, V Winter, D Curtis, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Alterations in glucocorticoid homeostasis following sleeve gastrectomySeraina O Moser, Andrei Moscalu, Cullen F Roberts, et al.
Progress in Clinical and Biological Research|January 1, 1992
Characterization of medium-chain acyl-CoA dehydrogenase (MCAD) with a point mutation associated with MCAD deficiencyP Bross, T Jensen, F Kräutle, et al.
Human Genetics|April 1, 1991
Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coliN Gregersen, B S Andresen, P Bross, et al.
Marine Environmental Research|April 26, 2025
An egg case study: Chronic exposure to AC electromagnetic fields results in hyperactivity in thornback ray (Raja clavata L.) embryosAnnemiek Hermans, Diede L Maas, Lydia M V de Barros Neta, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain acyl-CoA dehydrogenase deficiencyN Gregersen, B S Andresen, P Bross, et al.
Biochimica Et Biophysica Acta|October 20, 1993
Co-overexpression of bacterial GroESL chaperonins partly overcomes non-productive folding and tetramer assembly of E. coli-expressed human medium-chain acyl-CoA dehydrogenase (MCAD) carrying the prevalent disease-causing K304E mutationP Bross, B S Andresen, V Winter, et al.
British Journal of Pharmacology|September 23, 2023
Identification of a human blood biomarker of pharmacological 11β-hydroxysteroid dehydrogenase 1 inhibitionCristina Gómez, Zerin Alimajstorovic, Nantia Othonos, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular genetic characterization and urinary excretion pattern of metabolites in two families with MCAD deficiency due to compound heterozygosity with a 13 base pair insertion in one alleleN Gregersen, V Winter, S Lyonnet, et al.
Pageof 9

Showing results (51-60 of 85) with videos related to

Sort By:
Pageof 9
Infection and Immunity|July 19, 2000
Cloning of genes of nontypeable Haemophilus influenzae involved in penetration between human lung epithelial cellsM van Schilfgaarde, P van Ulsen, W van Der Steeg, et al.
Human Heredity|November 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from northwestern EuropeN Gregersen, V Winter, D Curtis, et al.
Biorxiv : the Preprint Server for Biology|September 15, 2025
Alterations in glucocorticoid homeostasis following sleeve gastrectomySeraina O Moser, Andrei Moscalu, Cullen F Roberts, et al.
Progress in Clinical and Biological Research|January 1, 1992
Characterization of medium-chain acyl-CoA dehydrogenase (MCAD) with a point mutation associated with MCAD deficiencyP Bross, T Jensen, F Kräutle, et al.
Human Genetics|April 1, 1991
Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coliN Gregersen, B S Andresen, P Bross, et al.
Marine Environmental Research|April 26, 2025
An egg case study: Chronic exposure to AC electromagnetic fields results in hyperactivity in thornback ray (Raja clavata L.) embryosAnnemiek Hermans, Diede L Maas, Lydia M V de Barros Neta, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain acyl-CoA dehydrogenase deficiencyN Gregersen, B S Andresen, P Bross, et al.
Biochimica Et Biophysica Acta|October 20, 1993
Co-overexpression of bacterial GroESL chaperonins partly overcomes non-productive folding and tetramer assembly of E. coli-expressed human medium-chain acyl-CoA dehydrogenase (MCAD) carrying the prevalent disease-causing K304E mutationP Bross, B S Andresen, V Winter, et al.
British Journal of Pharmacology|September 23, 2023
Identification of a human blood biomarker of pharmacological 11β-hydroxysteroid dehydrogenase 1 inhibitionCristina Gómez, Zerin Alimajstorovic, Nantia Othonos, et al.
Journal of Inherited Metabolic Disease|January 1, 1994
Molecular genetic characterization and urinary excretion pattern of metabolites in two families with MCAD deficiency due to compound heterozygosity with a 13 base pair insertion in one alleleN Gregersen, V Winter, S Lyonnet, et al.
Pageof 9