Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Daniela López-Espíndola"'
Autor:
Víctor Valcárcel-Hernández, Daniela López-Espíndola, Marina Guillén-Yunta, Ángel García-Aldea, Inés López de Toledo Soler, Soledad Bárez-López, Ana Guadaño-Ferraz
Publikováno v:
Neurobiology of Disease, Vol 162, Iss , Pp 105567- (2022)
Mutations in the thyroid hormone transporter monocarboxylate transporter 8 (MCT8) lead to profound brain alterations, including myelination impairments, in humans. We aimed to further explore the pathophysiological mechanisms underlying the MCT8 defi
Externí odkaz:
https://doaj.org/article/589a1f6799c14691a43c1635754f92f2
Autor:
Carolina Flores-Muñoz, Francisca García-Rojas, Miguel A. Pérez, Odra Santander, Elena Mery, Stefany Ordenes, Javiera Illanes-González, Daniela López-Espíndola, Arlek M. González-Jamett, Marco Fuenzalida, Agustín D. Martínez, Álvaro O. Ardiles
Publikováno v:
Cells, Vol 11, Iss 22, p 3646 (2022)
Enhanced activity and overexpression of Pannexin 1 (Panx1) channels contribute to neuronal pathologies such as epilepsy and Alzheimer’s disease (AD). The Panx1 channel ablation alters the hippocampus’s glutamatergic neurotransmission, synaptic pl
Externí odkaz:
https://doaj.org/article/b2ec816e17904dd487b66dbd7a5d8337
Autor:
Vanessa Dela Justina, Sebastian San Martin, Daniela López-Espíndola, Alecsander F. M. Bressan, Raiany Alves de Freitas, Ana Maria Lopes de Passos, Juan Varas, Victor V. Lima, Fernanda R. Giachini
Publikováno v:
European Journal of Histochemistry, Vol 63, Iss 4 (2019)
Signal transducer and activator of transcription 3 (STAT3) is a transcription factor that is activated by interleukin (IL)-6 and IL-10 that generate nearly opposing responses. The suppressor of cytokine signaling 3 (SOCS3) is the negative regulator o
Externí odkaz:
https://doaj.org/article/fd9b5c54c90f4898bff3aa3b6bd3ff22
Autor:
Carlos Escudero, Ellen Kupka, Belen Ibañez, Hermes Sandoval, Felipe Troncoso, Anna-Karin Wikström, Daniela López-Espíndola, Jesenia Acurio, Pablo Torres-Vergara, Lina Bergman
Publikováno v:
Hypertension (Dallas, Tex. : 1979).
Preeclampsia is a maternal syndrome characterized by the new onset of hypertension and proteinuria after 20 weeks of gestation associated with multisystemic complications, including brain alterations. Indeed, brain complications associated with preec
Autor:
Soledad Bárez-López, Daniela López-Espíndola, Marina Guillén-Yunta, Ana Guadaño-Ferraz, Víctor Valcárcel-Hernández, Inés López de Toledo Soler, A. García-Aldea
Publikováno v:
Neurobiology of Disease, Vol 162, Iss, Pp 105567-(2022)
Valcárcel-Hernández, V, López-Espíndola, D, Guillén-Yunta, M, García-Aldea, Á, López de Toledo Soler, I, Bárez-López, S & Guadaño-Ferraz, A 2022, ' Deficient thyroid hormone transport to the brain leads to impairments in axonal caliber and oligodendroglial development ', Neurobiology of Disease, vol. 162, 105567, pp. 105567 . https://doi.org/10.1016/j.nbd.2021.105567
Valcárcel-Hernández, V, López-Espíndola, D, Guillén-Yunta, M, García-Aldea, Á, López de Toledo Soler, I, Bárez-López, S & Guadaño-Ferraz, A 2022, ' Deficient thyroid hormone transport to the brain leads to impairments in axonal caliber and oligodendroglial development ', Neurobiology of Disease, vol. 162, 105567, pp. 105567 . https://doi.org/10.1016/j.nbd.2021.105567
Mutations in the thyroid hormone transporter monocarboxylate transporter 8 (MCT8) lead to profound brain alterations, including myelination impairments, in humans. We aimed to further explore the pathophysiological mechanisms underlying the MCT8 defi
Autor:
Inés Gómez de la Riva, A. García-Aldea, Juan Bernal, Ana Guadaño-Ferraz, Daniela López-Espíndola, Ana Margarita Rodríguez-García, Theo J. Visser, Domenico Salvatore
Publikováno v:
Brain Structure & Function, 224(6), 2103-2119. Springer-Verlag
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
Thyroid hormones (TH) are crucial for brain development; their deficiency during neurodevelopment impairs neural cell differentiation and causes irreversible neurological alterations. Understanding TH action, and in particular the mechanisms regulati
Autor:
Mareike Albert, C. Álvarez-Zaragoza, Brenda Angulo, Pauline Maciel August, Eva Ausó, André Rocha Barbosa, Renata Bartesaghi, Soledad Bárez-López, Dafna Ben Bashat, Liat Ben-Sira, Johanna Bendas, Christine Bibby, John W. Bigbee, Byron K.Y. Bitanihirwe, James A. Bourne, Antoine Bouyeure, Helena Brentani, J. Peter H. Burbach, Joshua A. Burk, F.J. Calabro, Victor Hugo Calegari de Toledo, Rita M. Cantor, Brian Chiou, Clodagh Cogley, Ilona Croy, Jorge Davila, Cheryl L. Dickter, Silvia Diviccaro, Stephanie D’Souza, Jeroen Dudink, Claire Enea-Drapeau, Carmen Espinós, Sade J. Faneyte, Arthur Sant’Anna Feltrin, Hilde Feys, Gianluca Gallo, A.A. García-Contreras, Laura Gaspari, Silvia Giatti, Courtney Gilchrist, Juan Antonio González-Barrios, Marisel González-Maya, Mihaela Grigore, Ana-Maria Grigore, Carmen Grijota-Martínez, Carlos M. Gómez, Ana Guadaño-Ferraz, Sandra Guidi, Loredana-Maria Himiniuc, Freek E. Hoebeek, Janine Hoffmann, Kurt L. Hoffman, Jihane Homman-Ludiye, Kiho Im, Iris Žunić Išasegi, Keiichi Ishihara, Ismael Jiménez-Estrada, Vijaya Kancherla, Tomohisa Katada, Ana Katušić, Sahar Kiani, Jeongtae Kim, Gregory W. Kirschen, Masaaki Kitada, Caroline Peres Klein, Katrijn Klingels, Shiori Kobayashi, Yoshinori Kosaka, Ivica Kostović, Mirna Kostović Srzentić, Željka Krsnik, Jennifer K. Lowe, Daniela López-Espíndola, B. Luna, Vincenzo Lupo, Zilu Ma, Lisa Mailleux, Louis N. Manganas, Vladimir Martínez-Álvarez, Mariana Maschietto, Cristiane Matté, Nadia McMillan, Roberto Cosimo Melcangi, Angel I. Melo, Elka Miller, Sara Mirsadeghi, A.J. Mitchell, Edwin A. Mitchell, Esraa Mohamed, Ruth Monaghan, Ana Montero-Pedrazuela, C.W. Musket, Marion Noulhiane, Tadahiro Numakawa, Haruki Odaka, Akihito Okabe, Fiadhnait O’Keeffe, Els Ortibus, Xianhua Piao, Hector Ramiro Quintá, A. Rea-Rosas, Aiguo Ren, Elena I. Rodríguez-Martínez, Liangyou Rui, Francisco J. Ruíz-Martínez, Hiroyuki Sakurai, Paula Sancho, Carmen Sato-Bigbee, Matthew Selby, Himanshu Sharma, Chigusa Shimizu-Okabe, Cristina Simon-Martinez, M.-O. Soyer-Gobillard, Fiorenza Stagni, Elinor L. Sullivan, Charles Sultan, Masanobu Sunagawa, Ana Carolina Tahira, Chitoshi Takayama, Akihito Takeuchi, Abhijeet Taori, Margot J. Taylor, B. Tervo-Clemmens, Verena Theis, Carsten Theiss, Deanne Kim Thompson, John M.D. Thompson, Bogdan Florin Toma, Raphaele Tsao, Charline Urbain, Verônica Luiza Vale Euclydes Colovati, E.M. Vásquez-Garibay, Karen E. Waldie, Linlin Wang, Tsung-Ung Wilson Woo, Paul Yao, René Zempoalteca, Nanyin Zhang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a3934ab2fbb127732ebb9edcbfe6b4d
https://doi.org/10.1016/b978-0-12-817986-4.01002-6
https://doi.org/10.1016/b978-0-12-817986-4.01002-6
Autor:
Soledad Bárez-López, Ana Guadaño-Ferraz, Carmen Grijota-Martínez, Ana Montero-Pedrazuela, Daniela López-Espíndola, Eva Ausó
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Thyroid hormones (T3 and T4) are essential for the development and function of the mammalian central nervous system (CNS). For this reason, controlling the availability of thyroid hormones to neural cells is an essential step. This is probably why th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15925bb47b93be8af93347170705a099
http://hdl.handle.net/10261/266075
http://hdl.handle.net/10261/266075
Autor:
Daniela López-Espíndola, Samuel Refetoff, Dorit Lev, Ella Sugo, Carmen Grijota-Martínez, Ana Guadaño-Ferraz, Carmen Morales-Bastos, Charles F. Verge, Juan Bernal, Xiao Hui Liao
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
et al.
[Context]: Mutations in the MCT8 (SLC16A2) gene, encoding a specific thyroid hormone transporter, cause an X-linked disease with profound psychomotor retardation, neurological impairment, and abnormal serumt hyroid hormone levels. The nat
[Context]: Mutations in the MCT8 (SLC16A2) gene, encoding a specific thyroid hormone transporter, cause an X-linked disease with profound psychomotor retardation, neurological impairment, and abnormal serumt hyroid hormone levels. The nat
Autor:
Flores-Muñoz, Carolina1,2,3 (AUTHOR), García-Rojas, Francisca3,4 (AUTHOR), Pérez, Miguel A.4,5 (AUTHOR), Santander, Odra3,4 (AUTHOR), Mery, Elena1,2 (AUTHOR), Ordenes, Stefany1,2,3 (AUTHOR), Illanes-González, Javiera1,2,3 (AUTHOR), López-Espíndola, Daniela6,7 (AUTHOR), González-Jamett, Arlek M.1,8 (AUTHOR), Fuenzalida, Marco4 (AUTHOR) marco.fuenzalida@uv.cl, Martínez, Agustín D.1 (AUTHOR) marco.fuenzalida@uv.cl, Ardiles, Álvaro O.1,2,9 (AUTHOR) marco.fuenzalida@uv.cl
Publikováno v:
Cells (2073-4409). Nov2022, Vol. 11 Issue 22, p3646. 31p.