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

M Grüneberg

Showing results (1-10 of 8) with videos related to

Pageof 1
Sort By:
Genomics|January 1, 1992
A long-range repeat cluster in chromosome 1 of the house mouse, Mus musculus, and its relation to a germline homogeneously staining regionL Purmann, C Plass, M Grüneberg, et al.
Plant Molecular Biology|January 14, 1998
Mitochondrial malate dehydrogenases in Brassica napus: altered protein patterns in different nuclear mitochondrial combinationsU Witt, R Lührs, F Buck, et al.
Neuropediatrics|October 1, 1992
Disturbance of GABA metabolism in pyridoxine-dependent seizuresG Kurlemann, R Ziegler, M Grüneberg, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1994
Assessment of tubular reabsorption of sodium, glucose, phosphate and amino acids based on spot urine samplesR Rossi, S Danzebrink, K Linnenbürger, et al.
JIMD Reports|August 5, 2015
TMEM165 Deficiency: Postnatal Changes in GlycosylationS Schulte Althoff, M Grüneberg, J Reunert, et al.
Deutsche Medizinische Wochenschrift (1946)|January 16, 2004
[Patient classification and analysis of risk profiles for type 2 diabetics as the main focus point in practice. Results of the TEMPO study]B Lippmann-Grob, R A Bierwirth, P Kron, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approachK Dörre, M Olczak, Y Wada, et al.
Journal of Human Genetics|April 6, 2018
QIL1-dependent assembly of MICOS complex-lethal mutation in C19ORF70 resulting in liver disease and severe neurological retardationJ Gödiker, M Grüneberg, I DuChesne, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Genomics|January 1, 1992
A long-range repeat cluster in chromosome 1 of the house mouse, Mus musculus, and its relation to a germline homogeneously staining regionL Purmann, C Plass, M Grüneberg, et al.
Plant Molecular Biology|January 14, 1998
Mitochondrial malate dehydrogenases in Brassica napus: altered protein patterns in different nuclear mitochondrial combinationsU Witt, R Lührs, F Buck, et al.
Neuropediatrics|October 1, 1992
Disturbance of GABA metabolism in pyridoxine-dependent seizuresG Kurlemann, R Ziegler, M Grüneberg, et al.
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1994
Assessment of tubular reabsorption of sodium, glucose, phosphate and amino acids based on spot urine samplesR Rossi, S Danzebrink, K Linnenbürger, et al.
JIMD Reports|August 5, 2015
TMEM165 Deficiency: Postnatal Changes in GlycosylationS Schulte Althoff, M Grüneberg, J Reunert, et al.
Deutsche Medizinische Wochenschrift (1946)|January 16, 2004
[Patient classification and analysis of risk profiles for type 2 diabetics as the main focus point in practice. Results of the TEMPO study]B Lippmann-Grob, R A Bierwirth, P Kron, et al.
Journal of Inherited Metabolic Disease|March 18, 2015
A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approachK Dörre, M Olczak, Y Wada, et al.
Journal of Human Genetics|April 6, 2018
QIL1-dependent assembly of MICOS complex-lethal mutation in C19ORF70 resulting in liver disease and severe neurological retardationJ Gödiker, M Grüneberg, I DuChesne, et al.
Pageof 1