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

Adelbert A Roscher

Showing results (31-40 of 39) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 39 results.
American Journal of Human Genetics|June 10, 2008
Loss of function in phenylketonuria is caused by impaired molecular motions and conformational instabilitySøren W Gersting, Kristina F Kemter, Michael Staudigl, et al.
Biochimica Et Biophysica Acta|December 14, 2005
Role of Pex19p in the targeting of PMP70 to peroxisomeYoshinori Kashiwayama, Kota Asahina, Hiroyuki Shibata, et al.
Nature Medicine|December 7, 2007
Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung diseaseDominik Hartl, Philipp Latzin, Peter Hordijk, et al.
American Journal of Human Genetics|November 24, 2001
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiencyAndreas Holzinger, Esther M Maier, Cornelius Bück, et al.
Journal of Lipid Research|February 21, 2012
In situ assay of fatty acid β-oxidation by metabolite profiling following permeabilization of cell membranesRegina Ensenauer, Ralph Fingerhut, Sonja C Schriever, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 26, 2017
Modification of the fatty acid composition of an obesogenic diet improves the maternal and placental metabolic environment in obese pregnant miceMartina Gimpfl, Jan Rozman, Maik Dahlhoff, et al.
Human Molecular Genetics|February 25, 2010
Pahenu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivoSøren W Gersting, Florian B Lagler, Anna Eichinger, et al.
Plos Medicine|October 30, 2018
Late-pregnancy dysglycemia in obese pregnancies after negative testing for gestational diabetes and risk of future childhood overweight: An interim analysis from a longitudinal mother-child cohort studyDelphina Gomes, Rüdiger von Kries, Maria Delius, et al.
Human Mutation|July 13, 2006
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessmentSonja C Stadler, Roman Polanetz, Esther M Maier, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
American Journal of Human Genetics|June 10, 2008
Loss of function in phenylketonuria is caused by impaired molecular motions and conformational instabilitySøren W Gersting, Kristina F Kemter, Michael Staudigl, et al.
Biochimica Et Biophysica Acta|December 14, 2005
Role of Pex19p in the targeting of PMP70 to peroxisomeYoshinori Kashiwayama, Kota Asahina, Hiroyuki Shibata, et al.
Nature Medicine|December 7, 2007
Cleavage of CXCR1 on neutrophils disables bacterial killing in cystic fibrosis lung diseaseDominik Hartl, Philipp Latzin, Peter Hordijk, et al.
American Journal of Human Genetics|November 24, 2001
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiencyAndreas Holzinger, Esther M Maier, Cornelius Bück, et al.
Journal of Lipid Research|February 21, 2012
In situ assay of fatty acid β-oxidation by metabolite profiling following permeabilization of cell membranesRegina Ensenauer, Ralph Fingerhut, Sonja C Schriever, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 26, 2017
Modification of the fatty acid composition of an obesogenic diet improves the maternal and placental metabolic environment in obese pregnant miceMartina Gimpfl, Jan Rozman, Maik Dahlhoff, et al.
Human Molecular Genetics|February 25, 2010
Pahenu1 is a mouse model for tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency and promotes analysis of the pharmacological chaperone mechanism in vivoSøren W Gersting, Florian B Lagler, Anna Eichinger, et al.
Plos Medicine|October 30, 2018
Late-pregnancy dysglycemia in obese pregnancies after negative testing for gestational diabetes and risk of future childhood overweight: An interim analysis from a longitudinal mother-child cohort studyDelphina Gomes, Rüdiger von Kries, Maria Delius, et al.
Human Mutation|July 13, 2006
Newborn screening for 3-methylcrotonyl-CoA carboxylase deficiency: population heterogeneity of MCCA and MCCB mutations and impact on risk assessmentSonja C Stadler, Roman Polanetz, Esther M Maier, et al.
Pageof 4