Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Rossina Novas"'
Autor:
Pablo Fresia, Sabrina Pimentel, Victoria Iriarte, Laura Marques, Verónica Durán, Anderson Saravia, Rossina Novas, Tatiana Basika, Alejandra Ferenczi, Daniel Castells, Tatiana Saporiti, Ulises Cuore, Santiago Losiewicz, Federico Fernández, Gabriel Ciappesoni, Marco Dalla-Rizza, Alejo Menchaca
Publikováno v:
Agrociencia Uruguay, Vol 25, Iss 2, p e974 (2021)
‘Mosca de la bichera’ or simply ‘bichera’ are common names given in Uruguay and the region to the primary myiasis-causing species Cochliomyia hominivorax, the New World Screwworm (NWS) fly (Diptera: Calliphoridae). Myiasis happens when dipter
Externí odkaz:
https://doaj.org/article/496e2936e5fd401082c4e6358a84b138
Autor:
Rossina Novas, Magdalena Cardenas-Rodriguez, Paola Lepanto, Matías Fabregat, Magela Rodao, María Inés Fariello, Mauricio Ramos, Camila Davison, Gabriela Casanova, Lucía Alfaya, Federico Lecumberry, Gualberto González-Sapienza, Florencia Irigoín, Jose L. Badano
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-16 (2018)
Abstract Bardet-Biedl syndrome (BBS) is a ciliopathy characterized by retinal degeneration, obesity, polydactyly, renal disease and mental retardation. CCDC28B is a BBS-associated protein that we have previously shown plays a role in cilia length reg
Externí odkaz:
https://doaj.org/article/b12b6dca1e794eb5831efb3cd8564235
Autor:
Federico Fernández, U. Cuore, Tatiana Saporiti, Sabrina Pimentel, Anderson Saravia, Pablo Fresia, Alejo Menchaca, Rossina Novas, Alejandra Ferenczi, Verónica Durán, Daniel Castells, Victoria Iriarte, Marco Dalla-Rizza, Santiago Losiewicz, G. Ciappesoni, Laura Marques, Tatiana Basika
Publikováno v:
Agrociencia Uruguay. 25
‘Mosca de la bichera’ or simply ‘bichera’ are common names given in Uruguay and the region to the primary myiasis-causing species Cochliomyia hominivorax, the New World Screwworm (NWS) fly (Diptera: Calliphoridae). Myiasis happens when dipter
Autor:
Josep Rotllant, Sheila Castro-Sánchez, Jose L. Badano, María Álvarez-Satta, Paula Suárez-Bregua, Rossina Novas, Diana Valverde
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-2 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-2 (2020)
The multiple genetic approaches available for molecular diagnosis of human diseases have made possible to identify an increasing number of pathogenic genetic changes, particularly with the advent of next generation sequencing (NGS) technologies. Howe
Autor:
Federico Lecumberry, Lucía Alfaya, Camila Davison, Gabriela Casanova, Jose L. Badano, Paola Lepanto, Florencia Irigoín, Rossina Novas, Mauricio Ramos, María Inés Fariello, Magela Rodao, Matías Fabregat, Gualberto González-Sapienza, Magdalena Cardenas-Rodriguez
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-16 (2018)
Scientific Reports
COLIBRI
Universidad de la República
instacron:Universidad de la República
Scientific Reports
COLIBRI
Universidad de la República
instacron:Universidad de la República
Bardet-Biedl syndrome (BBS) is a ciliopathy characterized by retinal degeneration, obesity, polydactyly, renal disease and mental retardation. CCDC28B is a BBS-associated protein that we have previously shown plays a role in cilia length regulation w
Functional analysis of new human Bardet-Biedl syndrome loci specific variants in the zebrafish model
Autor:
María Álvarez-Satta, Sheila Castro-Sánchez, Paula Suárez-Bregua, Jose L. Badano, Rossina Novas, Josep Rotllant, Diana Valverde
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
instname
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-12 (2019)
12 pages, 7 figures, 4 tables.-- This article is licensed under a Creative Commons Attribution 4.0 International License
The multiple genetic approaches available for molecular diagnosis of human diseases have made possible to identify an increa
The multiple genetic approaches available for molecular diagnosis of human diseases have made possible to identify an increa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e766cee5efa2084e7acc29a411970f1
https://hdl.handle.net/11093/4055
https://hdl.handle.net/11093/4055
Publikováno v:
FEBS Letters. 589:3479-3491
Bardet–Biedl syndrome (BBS) is a genetically heterogeneous, pleiotropic disorder, characterized by both congenital and late onset defects. From the analysis of the mutational burden in patients to the functional characterization of the BBS proteins