Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Vaishali, Katju"'
Autor:
Ulfar Bergthorsson, Caroline J. Sheeba, Anke Konrad, Tony Belicard, Toni Beltran, Vaishali Katju, Peter Sarkies
Publikováno v:
BMC Biology, Vol 18, Iss 1, Pp 1-17 (2020)
Abstract Background Transposable elements (TEs) are an almost universal constituent of eukaryotic genomes. In animals, Piwi-interacting small RNAs (piRNAs) and repressive chromatin often play crucial roles in preventing TE transcription and thus rest
Externí odkaz:
https://doaj.org/article/323ddc11421c48e49e5b2465523f1783
Autor:
Brent W. Bever, Zachary P. Dietz, Jennifer A. Sullins, Ariana M. Montoya, Ulfar Bergthorsson, Vaishali Katju, Suzanne Estes
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
We provide a partial test of the mitonuclear sex hypothesis with the first controlled study of how male frequencies and rates of outcrossing evolve in response to mitonuclear mismatch by allowing replicate lineages of C. elegans nematodes containing
Externí odkaz:
https://doaj.org/article/e6e11d2cece34f0183a98e3076ac48b3
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 12, Iss 1 (2021)
AbstractDNA mismatch repair (MMR), an evolutionarily conserved repair pathway shared by prokaryotic and eukaryotic species alike, influences molecular evolution by detecting and correcting mismatches, thereby protecting genetic fidelity, reducing the
Externí odkaz:
https://doaj.org/article/7441b59ec3a642008662266877d103e9
Publikováno v:
Nature Ecology & Evolution. 4:1539-1548
Epigenetic regulation involves changes in gene expression independent of DNA sequence variation that are inherited through cell division. In addition to a fundamental role in cell differentiation, some epigenetic changes can also be transmitted trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b9b86d97ef8b90731339fda0403734b
https://doi.org/10.1038/s41559-020-01293-z
https://doi.org/10.1038/s41559-020-01293-z
Publikováno v:
G3 (Bethesda, Md.). 12(11)
The DNA transposon Tc1 was the first transposable element to be characterized in Caenorhabditis elegans and to date, remains the best-studied transposable element in Caenorhabditis worms. While Tc1 copy-number is regulated at approximately 30 copies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1df055458f04ed81a7c4e267526df947
https://pubmed.ncbi.nlm.nih.gov/35977391
https://pubmed.ncbi.nlm.nih.gov/35977391
The DNA transposon Tc1 was the first transposable element (TE) to be characterized in Caenorhabditis elegans and to date, remains the best-studied TE in Caenorhabditis worms. While Tc1 copy-number is regulated at approximately 30 copies in the labora
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c737ddd1b0a5da24587eda3b4ccda46
https://doi.org/10.1101/2022.02.02.478770
https://doi.org/10.1101/2022.02.02.478770
DNA mismatch repair (MMR), an evolutionarily conserved repair pathway shared by prokaryotic and eukaryotic species alike, influences molecular evolution by detecting and correcting mismatches that escape DNA polymerase proofreading, thereby protectin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::959131c01082f8527a74dea1e9dd5600
https://doi.org/10.1101/2021.07.12.452034
https://doi.org/10.1101/2021.07.12.452034
Publikováno v:
G3: Genes|Genomes|Genetics
G3: Genes, Genomes, Genetics, Vol 12, Iss 1 (2021)
G3: Genes, Genomes, Genetics, Vol 12, Iss 1 (2021)
DNA mismatch repair (MMR), an evolutionarily conserved repair pathway shared by prokaryotic and eukaryotic species alike, influences molecular evolution by detecting and correcting mismatches, thereby protecting genetic fidelity, reducing the mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab4e9b2184f5cd286699bfa1c1f42c82
https://pubmed.ncbi.nlm.nih.gov/34849777
https://pubmed.ncbi.nlm.nih.gov/34849777
Autor:
Donald G. Moerman, Anke Konrad, Ulfar Bergthorsson, Vaishali Katju, Stephane Flibotte, Robert H. Waterston, Jon Taylor
Publikováno v:
Proceedings of the National Academy of Sciences. 115:7386-7391
Gene duplication and deletion are pivotal processes shaping the structural and functional repertoire of genomes, with implications for disease, adaptation, and evolution. We employed a mutation accumulation (MA) framework partnered with high-throughp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::726d898a4875bf074872f460e9cc3f23
https://doi.org/10.1073/pnas.1801930115
https://doi.org/10.1073/pnas.1801930115
Epigenetic regulation involves changes in gene expression independent of DNA sequence variation that are inherited through cell division (Holliday, 2006). In addition to a fundamental role in cell differentiation, some epigenetic changes can also be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c763fab208d75bed07674c743a3afff
https://doi.org/10.1101/2019.12.29.890194
https://doi.org/10.1101/2019.12.29.890194