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1por Nagesh, Rashmi, Kiran Kumar, K.M., Naveen Kumar, M., Patil, Rajeshwari H., Sharma, S. Chidananda“…Further, the downstream activation and regulation of AP-1 transcription factors could be through stress activated c-Jun – N terminal Kinase (JNK) Mitogen Activated Protein Kinases (MAPKs) which downregulated both Jun and Fos mRNA transcripts in areca nut extract exposed KB cells. Thus, outcome of the study provides insights into mechanistic path of pathogenesis of areca related disorders. …”
Publicado 2021
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2por Wang, Yaodi, Wang, Linxi, Liu, Hongjun, Gou, Bei, Hu, Weiyao, Qin, Li, Shen, Wentao, Wang, Aiming, Cui, Hongguang, Dai, Zhaoji“…The isolated areca protoplasts maintain viability of 86.6% and have been successfully transformed with a green fluorescent protein (GFP)-tagged plasmid (pGreen0029-GFP, 6.0 kb) via the polyethylene glycol (PEG)-mediated transformation. …”
Publicado 2023
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3por Ortore, Rocco Pio, Leone, Maria Pia, Palumbo, Orazio, Petracca, Antonio, Trecca, Eleonora M. C., D’Ecclesia, Aurelio, Vigliaroli, Ciro Lucio, Micale, Lucia, Longo, Francesco, Melchionda, Salvatore, Castori, MarcoEnlace del recurso
Publicado 2021
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4por Dupain, Célia, Masliah‐Planchon, Julien, Gu, Céline, Girard, Elodie, Gestraud, Pierre, Du Rusquec, Pauline, Borcoman, Edith, Bello, Diana, Ricci, Francesco, Hescot, Ségolène, Sablin, Marie‐Paule, Tresca, Patricia, de Moura, Alexandre, Loirat, Delphine, Frelaut, Maxime, Vincent‐Salomon, Anne, Lecerf, Charlotte, Callens, Céline, Antonio, Samantha, Franck, Coralie, Mariani, Odette, Bièche, Ivan, Kamal, Maud, Le Tourneau, Christophe, Servois, VincentEnlace del recurso
Publicado 2020
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5“…We further provided evidence that this plasmid applied a new mode of theta-type replication mechanism: (1) the size of this plasmid was > 10-kb; (2) the minireplicon consisted of AT-rich (directed repeat, iteron) and DnaA sequences; (3) the minireplicon did not contain double-strand origin (DSO) and essential rep genes, and it also showed no single-strand origin (SSO) structure; (4) the intermediate single-stranded DNA products were not observed for pTE15 replication; (5) the minireplicon did not contain a typical essential replication protein, Rep, (6) its copy number was decreased by chloramphenicol treatment, and (7) genes in pTE15 replication region encoded truncated RepA (TRepA), RepB and RepC, which were replication-associated proteins, but they were not essential for pTE15 replication. …”
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