Results 261 to 270 of about 168,391 (336)
Biochemical Analysis of the Intrinsic Mcm4-Mcm6-Mcm7 DNA Helicase Activity
Zhiying You, Yuki Komamura, Yukio Ishimi
openalex +1 more source
SSB promotes DnaB helicase passage through DnaA complexes at the replication origin oriC for bidirectional replication. [PDF]
Akama Y+4 more
europepmc +1 more source
COmapper: high‐resolution mapping of meiotic crossovers by long‐read sequencing in Arabidopsis
Summary Meiotic crossovers rearrange existing genetic variation between homologous chromosomes, profoundly affecting genomic diversity. Crossovers are typically constrained to one to three events per chromosome pair, and their distribution is shaped by chromatin accessibility and DNA polymorphisms.
Dohwan Byun+13 more
wiley +1 more source
WRNexo is not required to maintain normal sex ratios in Drosophila: A CURE-Based Investigation. [PDF]
Bolterstein E+3 more
europepmc +1 more source
Co‐inoculation studies indicated that Botrytis cinerea interact with Botryosphaeriaceae members of the grapevine trunk disease complex modulating disease development and expression. ABSTRACT In a previous study of fungal endophytes associated with grapevine trunk disease (GTD) in New Zealand vineyards, Botrytis cinerea was recovered from the inner ...
Noureddine Besselma+3 more
wiley +1 more source
Study on the Degradation of Aflatoxin B1 by <i>Myroides odoratimimus</i> 3J2MO. [PDF]
Wang X+11 more
europepmc +1 more source
The study characterizes interactions between DnaB helicase and DnaG primase in Mycobacterium tuberculosis using small‐angle X‐ray scattering, surface plasmon resonance, and cross‐linking. The findings reveal that DnaG forms dimers in solution, which are destabilized upon DnaB binding.
Dayan A, Ilic S, Akabayov B
wiley +1 more source
Primosomal protein PriC rescues replication initiation stress by bypassing the DnaA-DnaB interaction step for DnaB helicase loading at <i>oriC</i>. [PDF]
Yoshida R+4 more
europepmc +1 more source
Structure−Activity Relationships of New 1‐Aryl‐1H‐Indole Derivatives as SARS‐CoV‐2 Nsp13 Inhibitors
SARS‐CoV‐2 nsp13 is a promising target to develop effective antivirals. Pursuing the studies, new indolyl derivatives to deepen SARs are designed. The newly synthesized N‐aryl indoles are active vs both nsp13‐associated activities. They exert antiviral activity vs SARS‐CoV‐2 infected cells with no cytotoxicity.
Valentina Noemi Madia+18 more
wiley +1 more source