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Journal of Inherited Metabolic Disease
|
February 24, 2001
Plasma creatinine assessment in creatine deficiency: A diagnostic pitfall
N M Verhoeven, W S Guérand, E A Struys, et al.
Molecular Genetics and Metabolism
|
March 6, 2007
A prevalent pathogenic GAMT mutation (c.59G>C) in Portugal
L S Almeida, L Vilarinho, P S Darmin, et al.
Biochemical and Biophysical Research Communications
|
October 30, 1990
Identification of pristanoyl-CoA oxidase activity in human liver and its deficiency in the Zellweger syndrome
R J Wanders, H J ten Brink, C W van Roermund, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 27, 2018
Single-molecule analysis of endogenous β-actin mRNA trafficking reveals a mechanism for compartmentalized mRNA localization in axons
Benita Turner-Bridger, Maximillian Jakobs, Leila Muresan, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
February 7, 2015
Systematic evaluation of tumoral 99mTc-MAA uptake using SPECT and SPECT/CT in 502 patients before 90Y radioembolization
Harun Ilhan, Anna Goritschan, Phillip Paprottka, et al.
Clinical Chemistry and Laboratory Medicine
|
October 26, 2012
Plasma choline and betaine correlate with serum folate, plasma S-adenosyl-methionine and S-adenosyl-homocysteine in healthy volunteers
Apolline Imbard, Yvo M Smulders, Rob Barto, et al.
European Journal of Pharmacology
|
September 3, 1998
Discrimination between plasma membrane and intracellular target sites of sphingosylphosphorylcholine
D Meyer zu Heringdorf, N Niederdräing, E Neumann, et al.
Cell Reports
|
February 17, 2015
Organization of Mitochondrial Gene Expression in Two Distinct Ribosome-Containing Assemblies
Kirsten Kehrein, Ramon Schilling, Braulio Vargas Möller-Hergt, et al.
Molecular Pharmacology
|
July 25, 2000
Evidence for Edg-3 receptor-mediated activation of I(K.ACh) by sphingosine-1-phosphate in human atrial cardiomyocytes
H M Himmel, D Meyer Zu Heringdorf, E Graf, et al.
Annals of Neurology
|
September 5, 2002
X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8
Alberto Bizzi, Marianna Bugiani, Gajja S Salomons, et al.
Page
of 199
Search research articles
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Showing results (1031-1040 of 1,983) with videos related to
Sort By:
Page
of 199
Journal of Inherited Metabolic Disease
|
February 24, 2001
Plasma creatinine assessment in creatine deficiency: A diagnostic pitfall
N M Verhoeven, W S Guérand, E A Struys, et al.
Molecular Genetics and Metabolism
|
March 6, 2007
A prevalent pathogenic GAMT mutation (c.59G>C) in Portugal
L S Almeida, L Vilarinho, P S Darmin, et al.
Biochemical and Biophysical Research Communications
|
October 30, 1990
Identification of pristanoyl-CoA oxidase activity in human liver and its deficiency in the Zellweger syndrome
R J Wanders, H J ten Brink, C W van Roermund, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 27, 2018
Single-molecule analysis of endogenous β-actin mRNA trafficking reveals a mechanism for compartmentalized mRNA localization in axons
Benita Turner-Bridger, Maximillian Jakobs, Leila Muresan, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
February 7, 2015
Systematic evaluation of tumoral 99mTc-MAA uptake using SPECT and SPECT/CT in 502 patients before 90Y radioembolization
Harun Ilhan, Anna Goritschan, Phillip Paprottka, et al.
Clinical Chemistry and Laboratory Medicine
|
October 26, 2012
Plasma choline and betaine correlate with serum folate, plasma S-adenosyl-methionine and S-adenosyl-homocysteine in healthy volunteers
Apolline Imbard, Yvo M Smulders, Rob Barto, et al.
European Journal of Pharmacology
|
September 3, 1998
Discrimination between plasma membrane and intracellular target sites of sphingosylphosphorylcholine
D Meyer zu Heringdorf, N Niederdräing, E Neumann, et al.
Cell Reports
|
February 17, 2015
Organization of Mitochondrial Gene Expression in Two Distinct Ribosome-Containing Assemblies
Kirsten Kehrein, Ramon Schilling, Braulio Vargas Möller-Hergt, et al.
Molecular Pharmacology
|
July 25, 2000
Evidence for Edg-3 receptor-mediated activation of I(K.ACh) by sphingosine-1-phosphate in human atrial cardiomyocytes
H M Himmel, D Meyer Zu Heringdorf, E Graf, et al.
Annals of Neurology
|
September 5, 2002
X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8
Alberto Bizzi, Marianna Bugiani, Gajja S Salomons, et al.
Page
of 199