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Publikováno v:
J Vis Exp
Single-cell methodologies have revolutionized the analysis of the transcriptomes of specific cell types. However, they often require species-specific genetic "toolkits," such as promoters driving tissue-specific expression of fluorescent proteins. Fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::262c87662a8e7606de245ac6c2a2e817
https://europepmc.org/articles/PMC9976942/
https://europepmc.org/articles/PMC9976942/
Autor:
A Adhemir Valera, S Alberto Manchego, C Nieves Sandoval, R Antonio Herrera, H Shirley Palacios, S Gina Castro
Publikováno v:
Revista de Investigaciones Veterinarias del Perú. 32:e20016
El objetivo del presente estudio fue la caracterización molecular del segmento 4 del virus de la tilapia de lago (TiLV) detectado en tilapias de cultivo de los departamentos de Piura (Costa) y San Martín (Selva) en un brote ocurrido en 2017-2018. E
Autor:
Edward Vuong, Jintao Luo, David H. A. Fitch, Karin Kiontke, R. Antonio Herrera, Douglas S. Portman, Erich M. Schwarz
Publikováno v:
Dev Cell
Summary Biological roles for most long non-coding RNAs (lncRNAs) remain mysterious. Here, using forward genetics, we identify lep-5, a lncRNA acting in the C. elegans heterochronic (developmental timing) pathway. Loss of lep-5 delays hypodermal matur
Publikováno v:
Viral Immunology. 21:141-152
Interferon-gamma (IFN-gamma) has potent antiviral activity in neurons which is affected by the production of nitric oxide (NO). This study examines the interactions between cannabinoid receptor-1 (CB(1)), IFNgamma-induced pathways, and inhibition of
Publikováno v:
Development (Cambridge, England). 143(5)
The heterochronic genes lin-28, let-7 and lin-41 regulate fundamental developmental transitions in animals, such as stemness versus differentiation and juvenile versus adult states. We identify a new heterochronic gene, lep-2, in Caenorhabditis elega
Autor:
Park, Reyna1, Herrera, R. Antonio1
Publikováno v:
Southeastern Biology. Jan-Dec2024, Vol. 71 Issue 1-4, p116-117. 2p.
Publikováno v:
Southeastern Biology. Jan-Dec2024, Vol. 71 Issue 1-4, p115-116. 2p.
Autor:
Yajun Tang, R. Antonio Herrera, Xiangyang Liu, Isabelle Richard, Jer R. Kuszak, Rebecca K. Zoltoski, L.A. Novak, Nalin M. Kumar
Publikováno v:
Investigative ophthalmologyvisual science. 48(6)
Gap junctions consist of two hexameric structures of connexin (Cx) molecules called connexons, which are located in the plasma membranes of two neighboring cells. So far, more than 20 connexin genes have been identified in vertebrates.1,2 Three conne
Publikováno v:
Otolaryngology–Head and Neck Surgery. 131
Problem: Mutations in the gap junction beta-2 (GJB2) gene, which encodes the connexin 26 protein, account for 50% of all the patients with autosomal recessive nonsyndromic hearing loss. Connexins are proteins that oligomerize to form a gap junction c