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CRISPR/Cas Genome Editing and Its Applications in Cereal Crop Improvement

Plant-Environment Interactions, Volume 7, Issue 2, April 2026.
ABSTRACT CRISPR/Cas‐based genome editing has emerged as a transformative tool for precise genetic improvement of cereal crops. Recent advances in CRISPR technologies, including Cas9, Cas12, Cas13, base editing, and prime editing, have enabled targeted modification of genes and regulatory elements controlling yield, stress tolerance, and grain ...
Sirisha Kaniganti, Himanshu Saini, A. K. Chaitanya, Niranjan Hegde, Priya Shah, Nakul D. Magar, Ramesh Rijal, Jeevan Jyoti Kaushik, Deepak Nanda, Sharad Sachan, Anand Kumar, Roopali Bhoite, Harsha Rayudu Jamedar   +12 more
wiley   +1 more source

Whole genome sequence analysis of <i>Bifidobacterium animalis</i> subsp. <i>lactis</i> KL101 and comparative genomics with BB12. [PDF]

J Anim Sci Technol
Kim K, Lee J, Kang SJ, Oh S.
europepmc   +1 more source

Sequence Display enables large-scale sequence-activity datasets for rapid protein evolution. [PDF]

Nat Biotechnol
Cheng L, Zheng X, Jiang SJ, Hu Y, Liu Y, Yang K, Rui J, Ding H, Zhang M, Yuan T, Lu Q, Ye H, Li CL, Guo Y, Tian Z, Qin A, Zhou B, Yang KK, Huang X, Xiao H.   +19 more
europepmc   +1 more source

Draft genome sequence of <i>Listeria aquatica</i> strain SM_LAD isolated from cow dung in Bangladesh. [PDF]

Microbiol Resour Announc
Rahman SMM, Ahmed S.
europepmc   +1 more source

Regulated transformation system (RTS): sddi-mediated programmable shut-off and mode switching of base editors. [PDF]

Nucleic Acids Res
Deng J, Zhou J, Xiang H, Li X, Han X, Weng Z, Jia J, Shao Y, Sima Y, Niu M, Li D, Ouyang H, Xu B, Pang D, Yang L, Yuan H.   +15 more
europepmc   +1 more source

Editing mitochondrial and chloroplast genomes : Genome editing technologies for plant organelles provide new opportunities in functional genomics and breeding. [PDF]

EMBO Rep
Forner J, Bock R.
europepmc   +1 more source

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Purification of human DNA (cytosine‐5‐)‐methyltransferase

Journal of Cellular Biochemistry, 1985
AbstractWe have developed a facile procedure for the purification of DNA methyltransferase activity from human placenta. The procedure avoids the isolation of nuclei and the dialysis and chromatography of large volumes. A purification of 38,000‐fold from the whole cell extract has been achieved.
K E, Zucker, A D, Riggs, S S, Smith
openaire   +2 more sources