Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Francisco J. Rodríguez-Álvarez"'
Autor:
Marta Gandía, Francisco J. del Castillo, Francisco J. Rodríguez-Álvarez, Gema Garrido, Manuela Villamar, Manuela Calderón, Miguel A. Moreno-Pelayo, Felipe Moreno, Ignacio del Castillo
Publikováno v:
PLoS ONE, Vol 9, Iss 1 (2014)
Externí odkaz:
https://doaj.org/article/b192938e656f4c81a605022667bc2efa
Autor:
Luis Del Pozo-Yauner, Guillermo A. Herrera, Julio I. Perez Carreon, Elba A. Turbat-Herrera, Francisco J. Rodriguez-Alvarez, Robin A. Ruiz Zamora
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
The adaptive immune system of jawed vertebrates generates a highly diverse repertoire of antibodies to meet the antigenic challenges of a constantly evolving biological ecosystem. Most of the diversity is generated by two mechanisms: V(D)J gene recom
Externí odkaz:
https://doaj.org/article/5b59815683ab4cb99d72bbcc07d52429
Autor:
María Caballero, Beatriz I. Gallego, Mª José Toro, Francisco J. Rodríguez-Álvarez, Eva Jiménez-Mora, Antonio Chiloeches
Publikováno v:
Molecular and cellular biochemistry. 411(1-2)
Somatostatin (SST) is one of the main regulators of thyroid function. It acts by binding to its receptors, which lead to the dissociation of G proteins into Gαi and Gβγ subunits. However, much less is known about the function of Gβγ in thyroid c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78fb250f520f6aab76f08400bc6ef5df
https://pubmed.ncbi.nlm.nih.gov/26472731
https://pubmed.ncbi.nlm.nih.gov/26472731
Autor:
Gema Garrido, Ignacio del Castillo, M A Moreno-Pelayo, Felipe Moreno, Manuela Calderón, Manuela Villamar, Francisco J. del Castillo, Francisco J. Rodríguez-Álvarez, Marta Gandía
Publikováno v:
PLoS ONE, Vol 9, Iss 1 (2014)
PLoS ONE
PLoS ONE
Several errors were introduced in the preparation of this article for publication. The word "connexin" has been incorrectly substituted by "connection" throughout the article.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afbc6c1845d34e5317f97bc7efc4a9d8
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882183/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3882183/?tool=EBI
Autor:
Francisco J. Rodríguez-Álvarez, Marta Gandía, M A Moreno-Pelayo, Felipe Moreno, Manuela Villamar, Gema Garrido, Francisco J. del Castillo, Manuela Calderón, Ignacio del Castillo
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e73566 (2013)
PLoS ONE
PLoS ONE
The DFNB1 subtype of autosomal recessive, nonsyndromic hearing impairment, caused by mutations affecting the GJB2 (connexin-26) [corrected] gene, is highly prevalent in most populations worldwide. DFNB1 hearing impairment is mostly severe or profound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f509673a0290f963122b4d3a2e86d92a
http://europepmc.org/articles/PMC3765306?pdf=render
http://europepmc.org/articles/PMC3765306?pdf=render
Autor:
Marta Gandía, Francisco J Del Castillo, Francisco J Rodríguez-Álvarez, Gema Garrido, Manuela Villamar, Manuela Calderón, Miguel A Moreno-Pelayo, Felipe Moreno, Ignacio del Castillo
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e73566 (2013)
The DFNB1 subtype of autosomal recessive, nonsyndromic hearing impairment, caused by mutations affecting the GJB2 (connexin-26) [corrected] gene, is highly prevalent in most populations worldwide. DFNB1 hearing impairment is mostly severe or profound
Externí odkaz:
https://doaj.org/article/c42e1905cbc244e5a2a04a3e4aa2fece