Publications by authors named "W Kues"

Article Synopsis
  • - In xenotransplantation research, genetically modified pigs are crucial, with traditional methods like somatic cell nuclear transfer being lengthy and complex, prompting the need for more efficient gene editing techniques.
  • - The study explores the use of CRISPR/Cas9 and different delivery methods (electroporation vs. microinjection) to edit genes in pig zygotes, aiming to create triple-knock-out embryos targeting key porcine xenoantigens.
  • - Results showed that higher voltage during electroporation improved gene editing efficiency without significantly affecting embryo development, but mosaicism remained a common issue across all methods, highlighting the need for further optimization in genome editing approaches.
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Maternal germ plasm determines the germline in birds. Previously, we proposed the chicken-specific Bucky ball (cBuc) as a functional equivalent of the zebrafish germ plasm organizer. This study demonstrated the maternal cBuc synthesis, and verified a highly dynamic distribution of Bucky ball from oocyte nests to maturing follicles using specific antibodies.

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The study of the interactions between biofunctionalized gold nanoclusters (Au NCs) and spermatozoa is highly relevant to evaluate the potential of Au NCs as imaging probes and transfection agents in reproductive biology. In this work, confocal laser scanning microscopy (CLSM) was used to investigate the distribution of Au NCs bioconjugated with peptide (nuclear localisation sequence, NLS) and oligonucleotide (locked nucleic acid, LNA) ligands in bovine spermatozoa. Fluorescence lifetime imaging (FLIM) was employed to detect changes in the NC's chemical environment.

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The clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 system and somatic cell nuclear transfer (SCNT) have been used to produce genome-edited farm animal species for improved production and health traits; however, these tools are rarely used in the buffalo and can play a pivotal role in milk and meat production in tropical and subtropical countries. In this study, we aimed to produce myostatin () gene-edited embryos of the Murrah buffalo using the CRISPR/Cas9 system and SCNT. For this, fibroblast cells were electroporated with sgRNAs carrying all-in-one CRISPR/Cas9 plasmids targeting the first exon of the gene.

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