Results 141 to 150 of about 29,421 (241)

Erythrocytes loaded with phenylalanine ammonia lyase (PAL) as enzymatic replacement therapy for phenylketonuria

open access: yes, 2018
Phenylketonuria (PKU) is an inborn error of metabolism involving the enzyme phenylalanine (L-Phe) hydroxylase (PAH) which converts L-Phe to tyrosine (L-Tyr). Untreated PKU resulting in severe and enduring neurodevelopmental disorders, can be partially prevented by an early limitation of L-Phe intake.
openaire   +1 more source

Novel bacterium <i>Enterocloster</i> sp. M3 promotes colorectal tumorigenesis via the production of the carcinogen styrene. [PDF]

open access: yesGut Microbes
Zeng Y   +15 more
europepmc   +1 more source

Susceptibility of Yellow Clingstone Peach Cultivars to Inking Disorder. [PDF]

open access: yesInt J Mol Sci
Lopez-Raesfeld P   +4 more
europepmc   +1 more source

The Defense Responses of <i>Eucalyptus</i> to Insect-Feeding and Leaf-Clipping Stresses. [PDF]

open access: yesLife (Basel)
Chen C   +9 more
europepmc   +1 more source

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