Results 1 to 10 of about 2,664 (174)

Nucleoside deaminases: the key players in base editing toolkit. [PDF]

open access: yesBiophys Rep, 2023
The development of nucleoside deaminase-containing base editors realized targeted single base change with high efficiency and precision. Such nucleoside deaminases include adenosine and cytidine deaminases, which can catalyze adenosine-to-inosine (A-to-I) and cytidine-to-uridine (C-to-U) conversion respectively.
Xiang J   +5 more
europepmc   +5 more sources

Synthesis of 1,4-azaphosphinine nucleosides and evaluation as inhibitors of human cytidine deaminase and APOBEC3A [PDF]

open access: yesBeilstein Journal of Organic Chemistry
Nucleoside and polynucleotide cytidine deaminases (CDAs), such as CDA and APOBEC3, share a similar mechanism of cytosine to uracil conversion. In 1984, phosphapyrimidine riboside was characterised as the most potent inhibitor of human CDA, but the quick ...
Maksim V. Kvach   +5 more
doaj   +2 more sources

Nucleoside Analogs in ADAR Guide Strands Enable Editing at 5′-GA Sites [PDF]

open access: yesBiomolecules
Adenosine Deaminases Acting on RNA (ADARs) are members of a family of RNA editing enzymes that catalyze the conversion of adenosine into inosine in double-stranded RNA (dsRNA).
Aashrita Manjunath   +9 more
doaj   +2 more sources

Sex Differences in Metabolite-Immune Circuits of Neuroinflammation. [PDF]

open access: yesImmunol Rev
ABSTRACT Sex is a fundamental yet underexplored determinant of human neuroinflammation. Across autoimmune, neurodegenerative, and post‐infectious neurological syndromes, males and females exhibit consistent differences in disease vulnerability, progression, and immune tone.
Saminathan P   +6 more
europepmc   +2 more sources

Prokaryotic defense systems: Diversity and evolutionary adaptation. [PDF]

open access: yesmLife
Abstract Bacteriophages and archaeal viruses are the most abundant biological entities on Earth. Through a long‐standing co‐evolutionary arms race, they have driven the emergence of a diverse repertoire of prokaryotic defense systems. This review summarizes these systems, highlighting their diverse antiviral mechanisms across distinct stages of viral ...
Yang C, Gong L, Guo J, Xiang H.
europepmc   +2 more sources

Contribution of Cytidine Deaminase to Thymidylate Biosynthesis in Trypanosoma brucei: Intracellular Localization and Properties of the Enzyme

open access: yesmSphere, 2019
Cytidine deaminase (CDA) is a pyrimidine salvage enzyme that catalyzes cytidine and deoxycytidine hydrolytic deamination to yield uridine and deoxyuridine.
Ana Moro-Bulnes   +6 more
doaj   +1 more source

Combined familial adenosine deaminase and purine nucleoside phosphorylase deficiencies. [PDF]

open access: yesArchives of Disease in Childhood, 1988
We studied an Arab family in which two infants died of severe combined immunodeficiency caused by adenosine deaminase (ADA) deficiency. One infant had purine nucleoside phosphorylase (PNP) activity in the leucocytes only half that of normal. Four other infant siblings had previously died from infections before the age of 2 months.
A, Shanon   +4 more
openaire   +2 more sources

An interferon-like small chemical compound CDM-3008 suppresses hepatitis B virus through induction of interferon-stimulated genes.

open access: yesPLoS ONE, 2019
Oral administration of nucleotide analogues and injection of interferon-α (IFNα) are used to achieve immediate suppression in replication of hepatitis B virus (HBV).
Yutaka Furutani   +12 more
doaj   +1 more source

Nucleoside deaminase: an enzymatic marker for stress erythropoiesis in the mouse [PDF]

open access: yesJournal of Clinical Investigation, 1970
The level of nucleoside deaminase was determined in extracts of mouse tissues obtained during a period of accelerated erythropoiesis induced by hypoxia, hemorrhage, or the injection of phenylhydrazine. Under these conditions a striking (10- to 100-fold) elevation of the enzyme activity occurred in the spleen.
Rothman, I K   +3 more
openaire   +2 more sources

Dextran-Linked Purine Nucleosides as Substrates and Inhibitors of Adenosine Deaminase [PDF]

open access: yesEuropean Journal of Biochemistry, 1982
Dextran-bound adenosine, inosine, and nebularine have been prepared by carbodiimide coupling of their 2',3'-O-(4-carboxyethyl-1-methylbutylidene) cyclic acetal derivatives to 6-aminohexyldextran or 12-aminododecanyldextran. The latter polymers were prepared by cyanogen-bromide activation of dextran T80 followed by reaction with 1,6-diaminohexane or 1 ...
H, Rosemeyer, E, Körnig, F, Seela
openaire   +2 more sources

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