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

Rolfs

Showing results (391-400 of 712) with videos related to

Pageof 72
Sort By:
Molecular Biology Reports|February 4, 2019
Mutation analysis of genes related to methylmalonic acidemia: identification of eight novel mutationsFatemeh Keyfi, Mohammad R Abbaszadegan, Mojtaba Sankian, et al.
Nucleic Acids Research|November 30, 2006
PlasmID: a centralized repository for plasmid clone information and distributionDongmei Zuo, Stephanie E Mohr, Yanhui Hu, et al.
Organic & Biomolecular Chemistry|February 19, 2010
A new facile synthesis of 3-amidoindole derivatives and their evaluation as potential GSK-3beta inhibitorsAnahit Pews-Davtyan, Annegret Tillack, Anne-Caroline Schmöle, et al.
European Journal of Neurology|September 24, 2010
Frequency of Fabry disease in patients with small-fibre neuropathy of unknown aetiology: a pilot studyC Tanislav, M Kaps, A Rolfs, et al.
Gene|November 14, 1996
Dopamine D2 receptor gene (DRD2) haplotypes in CaucasiansU Finckh, M Giraldo-Velasquez, J Pelz, et al.
Journal of Neuroscience Research|November 18, 2014
Reduced cerebellar neurodegeneration after combined therapy with cyclodextrin/allopregnanolone and miglustat in NPC1: a mouse model of Niemann-Pick type C1 diseaseFabian Maass, Jana Petersen, Marina Hovakimyan, et al.
Frontiers in Pediatrics|March 22, 2021
Evaluating Patients' and Neonatologists' Satisfaction With the Use of Telemedicine for Neonatology Prenatal Consultations During the COVID-19 PandemicMaria C Lapadula, Shanna Rolfs, Edgardo G Szyld, et al.
Plos One|January 7, 2014
Olfactory deficits in Niemann-Pick type C1 (NPC1) diseaseMarina Hovakimyan, Anja Meyer, Jan Lukas, et al.
Circulation. Cardiovascular Genetics|January 8, 2014
Gene mutations versus clinically relevant phenotypes: lyso-Gb3 defines Fabry diseaseMarkus Niemann, Arndt Rolfs, Stefan Störk, et al.
Plos One|January 10, 2014
ADAM10 negatively regulates neuronal differentiation during spinal cord developmentXin Yan, Juntang Lin, Venkata Ajay Narendra Talabattula, et al.
Pageof 72

Showing results (391-400 of 712) with videos related to

Sort By:
Pageof 72
Molecular Biology Reports|February 4, 2019
Mutation analysis of genes related to methylmalonic acidemia: identification of eight novel mutationsFatemeh Keyfi, Mohammad R Abbaszadegan, Mojtaba Sankian, et al.
Nucleic Acids Research|November 30, 2006
PlasmID: a centralized repository for plasmid clone information and distributionDongmei Zuo, Stephanie E Mohr, Yanhui Hu, et al.
Organic & Biomolecular Chemistry|February 19, 2010
A new facile synthesis of 3-amidoindole derivatives and their evaluation as potential GSK-3beta inhibitorsAnahit Pews-Davtyan, Annegret Tillack, Anne-Caroline Schmöle, et al.
European Journal of Neurology|September 24, 2010
Frequency of Fabry disease in patients with small-fibre neuropathy of unknown aetiology: a pilot studyC Tanislav, M Kaps, A Rolfs, et al.
Gene|November 14, 1996
Dopamine D2 receptor gene (DRD2) haplotypes in CaucasiansU Finckh, M Giraldo-Velasquez, J Pelz, et al.
Journal of Neuroscience Research|November 18, 2014
Reduced cerebellar neurodegeneration after combined therapy with cyclodextrin/allopregnanolone and miglustat in NPC1: a mouse model of Niemann-Pick type C1 diseaseFabian Maass, Jana Petersen, Marina Hovakimyan, et al.
Frontiers in Pediatrics|March 22, 2021
Evaluating Patients' and Neonatologists' Satisfaction With the Use of Telemedicine for Neonatology Prenatal Consultations During the COVID-19 PandemicMaria C Lapadula, Shanna Rolfs, Edgardo G Szyld, et al.
Plos One|January 7, 2014
Olfactory deficits in Niemann-Pick type C1 (NPC1) diseaseMarina Hovakimyan, Anja Meyer, Jan Lukas, et al.
Circulation. Cardiovascular Genetics|January 8, 2014
Gene mutations versus clinically relevant phenotypes: lyso-Gb3 defines Fabry diseaseMarkus Niemann, Arndt Rolfs, Stefan Störk, et al.
Plos One|January 10, 2014
ADAM10 negatively regulates neuronal differentiation during spinal cord developmentXin Yan, Juntang Lin, Venkata Ajay Narendra Talabattula, et al.
Pageof 72