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Molecular Genetics and Metabolism
|
January 4, 2011
Elevated concentrations of sedoheptulose in bloodspots of patients with cystinosis caused by the 57-kb deletion: implications for diagnostics and neonatal screening
M M C Wamelink, E A Struys, E E W Jansen, et al.
European Journal of Epidemiology
|
June 19, 2010
Influence of short-term exposure to ultrafine and fine particles on systemic inflammation
Sabine Hertel, Anja Viehmann, Susanne Moebus, et al.
The EMBO Journal
|
June 10, 1998
Sphingosine kinase-mediated Ca2+ signalling by G-protein-coupled receptors
D Meyer zu Heringdorf, H Lass, R Alemany, et al.
Neurology
|
November 30, 2006
Blockade of chemokine signaling in patients with multiple sclerosis
F Zipp, H P Hartung, J Hillert, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 26, 2006
Glutaric aciduria type 1: clinical, biochemical and molecular findings in patients from Israel
Stanley H Korman, Cornelis Jakobs, Patricia S Darmin, et al.
Immunity
|
June 12, 2016
Inflammasome-Dependent Induction of Adaptive NK Cell Memory
Jasper G van den Boorn, Christopher Jakobs, Christian Hagen, et al.
The EMBO Journal
|
September 15, 2007
Direct stimulation of receptor-controlled phospholipase D1 by phospho-cofilin
Li Han, Matthias B Stope, Maider López de Jesús, et al.
Molecular Genetics and Metabolism
|
March 13, 2001
Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analyses
B M Hogema, S Akaboshi, M Taylor, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 2, 2005
Structure and mechanism of the reversible photoswitch of a fluorescent protein
Martin Andresen, Markus C Wahl, André C Stiel, et al.
The Biochemical Journal
|
April 30, 2004
Deletion of Ser-171 causes inactivation, proteasome-mediated degradation and complete deficiency of human transaldolase
Craig E Grossman, Brian Niland, Christina Stancato, et al.
Page
of 199
Search research articles
Search
Showing results (1301-1310 of 1,983) with videos related to
Sort By:
Page
of 199
Molecular Genetics and Metabolism
|
January 4, 2011
Elevated concentrations of sedoheptulose in bloodspots of patients with cystinosis caused by the 57-kb deletion: implications for diagnostics and neonatal screening
M M C Wamelink, E A Struys, E E W Jansen, et al.
European Journal of Epidemiology
|
June 19, 2010
Influence of short-term exposure to ultrafine and fine particles on systemic inflammation
Sabine Hertel, Anja Viehmann, Susanne Moebus, et al.
The EMBO Journal
|
June 10, 1998
Sphingosine kinase-mediated Ca2+ signalling by G-protein-coupled receptors
D Meyer zu Heringdorf, H Lass, R Alemany, et al.
Neurology
|
November 30, 2006
Blockade of chemokine signaling in patients with multiple sclerosis
F Zipp, H P Hartung, J Hillert, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 26, 2006
Glutaric aciduria type 1: clinical, biochemical and molecular findings in patients from Israel
Stanley H Korman, Cornelis Jakobs, Patricia S Darmin, et al.
Immunity
|
June 12, 2016
Inflammasome-Dependent Induction of Adaptive NK Cell Memory
Jasper G van den Boorn, Christopher Jakobs, Christian Hagen, et al.
The EMBO Journal
|
September 15, 2007
Direct stimulation of receptor-controlled phospholipase D1 by phospho-cofilin
Li Han, Matthias B Stope, Maider López de Jesús, et al.
Molecular Genetics and Metabolism
|
March 13, 2001
Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analyses
B M Hogema, S Akaboshi, M Taylor, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 2, 2005
Structure and mechanism of the reversible photoswitch of a fluorescent protein
Martin Andresen, Markus C Wahl, André C Stiel, et al.
The Biochemical Journal
|
April 30, 2004
Deletion of Ser-171 causes inactivation, proteasome-mediated degradation and complete deficiency of human transaldolase
Craig E Grossman, Brian Niland, Christina Stancato, et al.
Page
of 199