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Stephan Rust

Showing results (21-30 of 53) with videos related to

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Critical Care Medicine|March 21, 2002
Effect of the interleukin-6 promoter polymorphism (-174 G/C) on the incidence and outcome of sepsisBernhard Schlüter, Carsten Raufhake, Michael Erren, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 31, 2014
The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylationJulien H Park, Andrea Zühlsdorf, Yoshinao Wada, et al.
Alcohol and Alcoholism (Oxford, Oxfordshire)|September 4, 2015
It Is Not Always Alcohol Abuse--A Transferrin Variant Impairing the CDT TestAndrea Zühlsdorf, Michael Said, Christoph Seger, et al.
The Journal of Biological Chemistry|May 28, 2004
Impaired platelet activation in familial high density lipoprotein deficiency (Tangier disease)Jerzy-Roch Nofer, Grazyna Herminghaus, Martin Brodde, et al.
JIMD Reports|November 8, 2024
Expanding the genetic and clinical spectrum of SLC25A42-associated disorders and testing of pantothenic acid to improve CoA level in vitroKatharina Heckmann, Arcangela Iuso, Janine Reunert, et al.
Molecular Genetics and Metabolism Reports|September 5, 2020
SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylationThorsten Marquardt, Vladimir Bzduch, Max Hogrebe, et al.
FEBS Letters|May 19, 2004
ADP-ribosylation factor (ARF)-like 7 (ARL7) is induced by cholesterol loading and participates in apolipoprotein AI-dependent cholesterol exportThomas Engel, Aloys Lueken, Günther Bode, et al.
Metabolites|April 26, 2024
Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 DeficiencyMaximilian Penkl, Johannes A Mayr, René G Feichtinger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2017
SLC39A8 deficiency: biochemical correction and major clinical improvement by manganese therapyJulien H Park, Max Hogrebe, Manfred Fobker, et al.
Frontiers in Neurology|May 14, 2021
Severe Form of ßIV-Spectrin Deficiency With Mitochondrial Dysfunction and Cardiomyopathy-A Case ReportAziza Miriam Belkheir, Janine Reunert, Christiane Elpers, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Critical Care Medicine|March 21, 2002
Effect of the interleukin-6 promoter polymorphism (-174 G/C) on the incidence and outcome of sepsisBernhard Schlüter, Carsten Raufhake, Michael Erren, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 31, 2014
The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylationJulien H Park, Andrea Zühlsdorf, Yoshinao Wada, et al.
Alcohol and Alcoholism (Oxford, Oxfordshire)|September 4, 2015
It Is Not Always Alcohol Abuse--A Transferrin Variant Impairing the CDT TestAndrea Zühlsdorf, Michael Said, Christoph Seger, et al.
The Journal of Biological Chemistry|May 28, 2004
Impaired platelet activation in familial high density lipoprotein deficiency (Tangier disease)Jerzy-Roch Nofer, Grazyna Herminghaus, Martin Brodde, et al.
JIMD Reports|November 8, 2024
Expanding the genetic and clinical spectrum of SLC25A42-associated disorders and testing of pantothenic acid to improve CoA level in vitroKatharina Heckmann, Arcangela Iuso, Janine Reunert, et al.
Molecular Genetics and Metabolism Reports|September 5, 2020
SLC37A4-CDG: Mislocalization of the glucose-6-phosphate transporter to the Golgi causes a new congenital disorder of glycosylationThorsten Marquardt, Vladimir Bzduch, Max Hogrebe, et al.
FEBS Letters|May 19, 2004
ADP-ribosylation factor (ARF)-like 7 (ARL7) is induced by cholesterol loading and participates in apolipoprotein AI-dependent cholesterol exportThomas Engel, Aloys Lueken, Günther Bode, et al.
Metabolites|April 26, 2024
Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 DeficiencyMaximilian Penkl, Johannes A Mayr, René G Feichtinger, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 28, 2017
SLC39A8 deficiency: biochemical correction and major clinical improvement by manganese therapyJulien H Park, Max Hogrebe, Manfred Fobker, et al.
Frontiers in Neurology|May 14, 2021
Severe Form of ßIV-Spectrin Deficiency With Mitochondrial Dysfunction and Cardiomyopathy-A Case ReportAziza Miriam Belkheir, Janine Reunert, Christiane Elpers, et al.
Pageof 6