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Biochimie
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February 17, 2021
Succinyl-CoA:3-oxoacid coenzyme A transferase (SCOT) deficiency: A rare and potentially fatal metabolic disease
Sarah C Grünert, William Foster, Anke Schumann, et al.
The Journal of Biological Chemistry
|
October 10, 2006
Structural insights into the design of nonpeptidic isothiazolidinone-containing inhibitors of protein-tyrosine phosphatase 1B
Paul J Ala, Lucie Gonneville, Milton Hillman, et al.
Annals of the Rheumatic Diseases
|
May 11, 2025
Investigating endogenous immune-mediated monocyte memory in rheumatoid arthritis
Anna M Marzeda, Anja Schwenzer, Bogdan S Didov, et al.
The Journal of Biological Chemistry
|
August 19, 2006
Structural basis for inhibition of protein-tyrosine phosphatase 1B by isothiazolidinone heterocyclic phosphonate mimetics
Paul J Ala, Lucie Gonneville, Milton C Hillman, et al.
Neurogenetics
|
March 2, 2026
Expanding the genotypic spectrum of combined oxidative phosphorylation deficiency 54
King Lam Lai, Thomas B Smith, Reza Maroofian, et al.
Brain : a Journal of Neurology
|
September 9, 2016
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes
Emma S Reid, Apostolos Papandreou, Suzanne Drury, et al.
Blood
|
December 1, 2017
Nbeal2 interacts with Dock7, Sec16a, and Vac14
Louisa Mayer, Maria Jasztal, Mercedes Pardo, et al.
Kidney International
|
March 20, 2019
Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder
Neil A Roberts, Emma N Hilton, Filipa M Lopes, et al.
Journal of Medicinal Chemistry
|
June 11, 2009
Discovery of potent competitive inhibitors of indoleamine 2,3-dioxygenase with in vivo pharmacodynamic activity and efficacy in a mouse melanoma model
Eddy W Yue, Brent Douty, Brian Wayland, et al.
European Journal of Human Genetics : EJHG
|
August 9, 2023
Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54
Thomas B Smith, Alessandro Rea, Huw B Thomas, et al.
Page
of 26
Search research articles
Search
Showing results (211-220 of 254) with videos related to
Sort By:
Page
of 26
Biochimie
|
February 17, 2021
Succinyl-CoA:3-oxoacid coenzyme A transferase (SCOT) deficiency: A rare and potentially fatal metabolic disease
Sarah C Grünert, William Foster, Anke Schumann, et al.
The Journal of Biological Chemistry
|
October 10, 2006
Structural insights into the design of nonpeptidic isothiazolidinone-containing inhibitors of protein-tyrosine phosphatase 1B
Paul J Ala, Lucie Gonneville, Milton Hillman, et al.
Annals of the Rheumatic Diseases
|
May 11, 2025
Investigating endogenous immune-mediated monocyte memory in rheumatoid arthritis
Anna M Marzeda, Anja Schwenzer, Bogdan S Didov, et al.
The Journal of Biological Chemistry
|
August 19, 2006
Structural basis for inhibition of protein-tyrosine phosphatase 1B by isothiazolidinone heterocyclic phosphonate mimetics
Paul J Ala, Lucie Gonneville, Milton C Hillman, et al.
Neurogenetics
|
March 2, 2026
Expanding the genotypic spectrum of combined oxidative phosphorylation deficiency 54
King Lam Lai, Thomas B Smith, Reza Maroofian, et al.
Brain : a Journal of Neurology
|
September 9, 2016
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes
Emma S Reid, Apostolos Papandreou, Suzanne Drury, et al.
Blood
|
December 1, 2017
Nbeal2 interacts with Dock7, Sec16a, and Vac14
Louisa Mayer, Maria Jasztal, Mercedes Pardo, et al.
Kidney International
|
March 20, 2019
Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder
Neil A Roberts, Emma N Hilton, Filipa M Lopes, et al.
Journal of Medicinal Chemistry
|
June 11, 2009
Discovery of potent competitive inhibitors of indoleamine 2,3-dioxygenase with in vivo pharmacodynamic activity and efficacy in a mouse melanoma model
Eddy W Yue, Brent Douty, Brian Wayland, et al.
European Journal of Human Genetics : EJHG
|
August 9, 2023
Novel homozygous variants in PRORP expand the genotypic spectrum of combined oxidative phosphorylation deficiency 54
Thomas B Smith, Alessandro Rea, Huw B Thomas, et al.
Page
of 26