Results 181 to 190 of about 1,562,024 (293)

The DNA helicase HELQ promotes replication fork reversal in coordination with BRCA2- and FANCD2-mediated repair pathways. [PDF]

open access: yesNucleic Acids Res
Dunbayev Y   +10 more
europepmc   +1 more source

Tau Pathology Associated With Parkinsonism and Mutation of Mitochondrial DNA Helicase Gene TWNK. [PDF]

open access: yesNeurol Genet, 2021
Vandenberghe W   +6 more
europepmc   +1 more source

From biology to biotechnology: Host‐regulation factors from parasitoid wasps are a source of bioactive molecules with translational potential

open access: yesInsect Molecular Biology, EarlyView.
Parasitoid wasps deploy maternal and embryonic factors to reprogramme host physiology. Venom, calyx fluid, polydnaviruses, teratocytes and larval secretions act in a coordinated, compartmentalised manner. Host‐regulation factors are promising sources of insecticidal, antimicrobial and bioinspired translational molecules.
Ciro Pedro G. Pinto   +2 more
wiley   +1 more source

Deficiency of Werner RecQ-type DNA helicase causes premature malnutrition in zebrafish. [PDF]

open access: yesiScience
Ujibe K   +9 more
europepmc   +1 more source

RNA activation in insects: From emerging evidence to molecular applications

open access: yesInsect Molecular Biology, EarlyView.
Canonical RNA activation involves small RNAs interacting with promoter sequences, but there is also evidence of non‐canonical RNAa in eukaryotes. Emerging evidence suggests the presence of RNAa in insects. RNAa can be utilised as a tool for functional genomic studies in insects.
Sassan Asgari
wiley   +1 more source

An Adenosine Triphosphate- Dependent 5'-3' DNA Helicase From sk1-Like Lactococcus lactis F13 Phage. [PDF]

open access: yesFront Microbiol, 2022
Chmielewska-Jeznach M   +4 more
europepmc   +1 more source

Expanding the Clinical Spectrum of DHX30‐Related Neurodevelopmental Disorder: A Case Report and a Scoping Review

open access: yesJournal of Intellectual Disability Research, EarlyView.
ABSTRACT Background Whole exome sequencing (WES) has improved diagnostic rates for neurodevelopmental disorders (NDDs) while introducing challenges in novel variant interpretation. DHX30‐related NDD (DHX30‐NDD) is a recently described condition with an evolving phenotypic spectrum.
Nattaporn Tassanakijpanich   +3 more
wiley   +1 more source

Role of the DDX11 DNA Helicase in Warsaw Breakage Syndrome Etiology. [PDF]

open access: yesInt J Mol Sci, 2021
Santos D   +3 more
europepmc   +1 more source

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