Results 251 to 260 of about 141,947 (341)

Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.

open access: yesHuman Molecular Genetics, 2014
S. Houten   +12 more
semanticscholar   +1 more source

Disorders of Redox Homeostasis and Its Importance in Acrolein Toxicity. [PDF]

open access: yesInt J Mol Sci
Kwolek-Mirek M   +7 more
europepmc   +1 more source

Enzyme response to thyrotoxicosis and hypothyroidism in human liver and muscle [PDF]

open access: yes, 1972
Bachmaier, B.   +5 more
core  

hiPSCGEM01: A Genome-Scale Metabolic Model for Fibroblast-Derived Human iPSCs. [PDF]

open access: yesBioengineering (Basel)
Procopio A   +7 more
europepmc   +1 more source

Potassium binding by carbonyl clusters, halophilic adaptation and catalysis of Haloferax mediterranei D-2-hydroxyacid dehydrogenase. [PDF]

open access: yesCommun Biol
Domenech J   +11 more
europepmc   +1 more source

Kinetic Dissection of the Reaction of Human GDP-l-Fucose Synthase. [PDF]

open access: yesACS Catal
Smyshliaev D   +3 more
europepmc   +1 more source

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