Results 281 to 290 of about 754,035 (345)
FabricSpotDefect: An annotated dataset for identifying spot defects in different fabric types. [PDF]
Islam F, Sumaya, Monir MF, Islam A.
europepmc +1 more source
The Roc system represents a highly interconnected but incomplete network of two‐component regulatory systems involved in the virulence of Pseudomonas aeruginosa. Our work has enabled us to identify the missing RocA3 regulator, to propose new players in the system and to delineate their conservation between clades of the species.
Victor Simon+3 more
wiley +1 more source
Galaxy Helm chart: a standardized method for deploying production Galaxy servers. [PDF]
Goonasekera N+3 more
europepmc +1 more source
Summary Drought stress imposes severe challenges on agriculture by impacting crop performance. Understanding drought responses in plants at a cellular level is a crucial first step toward engineering improved drought resilience. However, the molecular responses to drought are complex as they depend on multiple factors, including the severity of drought,
Rubén Tenorio Berrío+6 more
wiley +1 more source
UBV starcounts in SA54 and global structure of the Galaxy
T. Yamagata, Yuzuru Yoshii
openalex +1 more source
GCN5‐related histone acetyltransferase HOOKLESS2 regulates fungal resistance and growth in tomato
Summary The functions of histone acetyltransferases (HATs) in the genetic control of crop traits and the underlying mechanisms are poorly understood. We studied the function of tomato HOOKLESS2 (SlHLS2), a member of the GCN5 family of HATs, through genetic, molecular and genomic approaches. Tomato hls2 mutants generated through CRISPR‐cas9 gene editing
Namrata Jaiswal+3 more
wiley +1 more source
Complete genome sequence of Bacillus subtilis bacteriophage Adastra. [PDF]
Herbig AF, Pendergrass EM.
europepmc +1 more source
Circadian clock disruption promotes retinal photoreceptor degeneration
Mice carrying a knock‐in of the P23H mutation of the rhodopsin gene are a well‐characterized model of retinitis pigmentosa (RP), a hereditary retinal degeneration affecting primarily rods. Here, by combining the P23H Rho mutation with the rod‐specific invalidation of the Bmal1 clock gene and by performing functional, structural, and molecular analyses,
Shumet T. Gegnaw+8 more
wiley +1 more source