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Biochemical and Biophysical Research Communications
|
August 15, 1991
Deletion-mutant epidermal growth factor receptor in human gliomas: effects of type II mutation on receptor function
P A Humphrey, L M Gangarosa, A J Wong, et al.
Journal of Inherited Metabolic Disease
|
March 9, 2019
Functional disruption of pyrimidine nucleoside transporter CNT1 results in a novel inborn error of metabolism with high excretion of uridine and cytidine
R A Wevers, M Christensen, U F H Engelke, et al.
Molecular Genetics and Metabolism
|
March 5, 2019
Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment
Femke Molema, Florian Gleich, Peter Burgard, et al.
Mbio
|
May 7, 2015
Genetic diversity in the collaborative cross model recapitulates human West Nile virus disease outcomes
Jessica B Graham, Sunil Thomas, Jessica Swarts, et al.
Smart Medicine
|
August 27, 2024
Single therapeutic dose of an antiviral UL29 siRNA swarm diminishes symptoms and viral load of mice infected intranasally with HSV-1
Tuomas Lasanen, Fanny Frejborg, Liisa M Lund, et al.
Pain
|
May 22, 2018
Peripherally restricted cannabinoid 1 receptor agonist as a novel analgesic in cancer-induced bone pain
Hong Zhang, Dominique M Lund, Haley A Ciccone, et al.
Clinical Genetics
|
July 28, 2015
Alpha-mannosidosis: characterization of CNS pathology and correlation between CNS pathology and cognitive function
L Borgwardt, E R Danielsen, C Thomsen, et al.
Journal of Inherited Metabolic Disease
|
February 9, 2019
Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry
Femke Molema, Florian Gleich, Peter Burgard, et al.
Molecular Genetics and Metabolism
|
October 23, 2012
Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III
Jessica de Ruijter, Minke H de Ru, Tom Wagemans, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
October 4, 2017
Hyperglucagonemia correlates with plasma levels of non-branched-chain amino acids in patients with liver disease independent of type 2 diabetes
Nicolai J Wewer Albrechtsen, Anders E Junker, Mette Christensen, et al.
Page
of 70
Search research articles
Search
Showing results (571-580 of 693) with videos related to
Sort By:
Page
of 70
Biochemical and Biophysical Research Communications
|
August 15, 1991
Deletion-mutant epidermal growth factor receptor in human gliomas: effects of type II mutation on receptor function
P A Humphrey, L M Gangarosa, A J Wong, et al.
Journal of Inherited Metabolic Disease
|
March 9, 2019
Functional disruption of pyrimidine nucleoside transporter CNT1 results in a novel inborn error of metabolism with high excretion of uridine and cytidine
R A Wevers, M Christensen, U F H Engelke, et al.
Molecular Genetics and Metabolism
|
March 5, 2019
Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment
Femke Molema, Florian Gleich, Peter Burgard, et al.
Mbio
|
May 7, 2015
Genetic diversity in the collaborative cross model recapitulates human West Nile virus disease outcomes
Jessica B Graham, Sunil Thomas, Jessica Swarts, et al.
Smart Medicine
|
August 27, 2024
Single therapeutic dose of an antiviral UL29 siRNA swarm diminishes symptoms and viral load of mice infected intranasally with HSV-1
Tuomas Lasanen, Fanny Frejborg, Liisa M Lund, et al.
Pain
|
May 22, 2018
Peripherally restricted cannabinoid 1 receptor agonist as a novel analgesic in cancer-induced bone pain
Hong Zhang, Dominique M Lund, Haley A Ciccone, et al.
Clinical Genetics
|
July 28, 2015
Alpha-mannosidosis: characterization of CNS pathology and correlation between CNS pathology and cognitive function
L Borgwardt, E R Danielsen, C Thomsen, et al.
Journal of Inherited Metabolic Disease
|
February 9, 2019
Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry
Femke Molema, Florian Gleich, Peter Burgard, et al.
Molecular Genetics and Metabolism
|
October 23, 2012
Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III
Jessica de Ruijter, Minke H de Ru, Tom Wagemans, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology
|
October 4, 2017
Hyperglucagonemia correlates with plasma levels of non-branched-chain amino acids in patients with liver disease independent of type 2 diabetes
Nicolai J Wewer Albrechtsen, Anders E Junker, Mette Christensen, et al.
Page
of 70