Zobrazeno 11 - 14
of 14
pro vyhledávání: '"Laia Gómez-Baldó"'
Publikováno v:
Hereditas. 145:154-162
A 793-nucleotide fragment from the D. subobscura Odh gene was sequenced in 46 lethal chromosomal lines from two South American colonizing populations (18 from Santiago de Chile and 28 from Puerto Montt). Only eight different haplotypes were found and
Autor:
Josep Balart, Miguel Angel Pujana, Helena Aguilar, Tommy Fornander, Yusuke Nakamura, Pasi Halonen, Xavier Barril, Miguel Gil, Olle Stål, Gizeh Pérez Tenorio, Maurice P.H.M. Jansen, Maria Teresa Soler, Rafael Garcia-Mata, Robert Clarke, Xosé R. Bustelo, Fina Climent, Núria Bonifaci, Ekaterina Nevedomskaya, Luciano Di Croce, John A. Katzenellenbogen, Ander Urruticoechea, Wilbert Zwart, Taisei Mushiroda, Elin Karlsson, Livia Caizzi, Hitoshi Zembutsu, Joan Brunet, Manel Esteller, Josefine Bostner, Kazuma Kiyotani, Dennis C. Sgroi, Kerry L. Burnstein, Laia Gómez-Baldó, Roderick L. Beijersbergen, Nadia García, Ana I. Extremera, Abul B. M. M. K. Islam, Alberto Villanueva, Kathryn E. Carlson, Jordi Serra-Musach, Alejo Rodríguez-Vida, Griselda Martrat, Miguel Vizoso, Ana B. Rodríguez-Peña, Agnès Figueras
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Digital.CSIC. Repositorio Institucional del CSIC
Dipòsit Digital de la UB
Universidad de Barcelona
Breast Cancer Research : BCR
instname
Digital.CSIC. Repositorio Institucional del CSIC
Dipòsit Digital de la UB
Universidad de Barcelona
Breast Cancer Research : BCR
This is an Open Access article distributed under the terms of the Creative Commons Attribution License.-- et al.
[Introduction]: Endocrine therapies targeting cell proliferation and survival mediated by estrogen receptor α (ERα) are among the
[Introduction]: Endocrine therapies targeting cell proliferation and survival mediated by estrogen receptor α (ERα) are among the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a68f8d1076656324b05b2778d5e39d6
http://hdl.handle.net/10261/134716
http://hdl.handle.net/10261/134716
Autor:
Isidre, Ferrer, Pooja, Mohan, Helen, Chen, Joan, Castellsague, Laia, Gómez-Baldó, Marga, Carmona, Nadia, García, Helena, Aguilar, Jihong, Jiang, Margaretha, Skowron, Mark, Nellist, Israel, Ampuero, Antonio, Russi, Conxi, Lázaro, Christopher A, Maxwell, Miguel Angel, Pujana
Publikováno v:
The Journal of pathology. 233(3)
Most patients with tuberous sclerosis complex (TSC) develop cortical tubers that cause severe neurological disabilities. It has been suggested that defects in neuronal differentiation and/or migration underlie the appearance of tubers. However, the p
Autor:
Piedad Ussetti, Julio Ancochea, Rosalía Laporta, Mar Varela, Jordi Serra-Musach, Raul Ortega, Antoni Xaubet, Francesca Mateo, Antonio Roman, María Jesús Pla, Jose V. Sanchez-Mut, Álvaro Casanova, Anna Petit, Catalina Falo, August Vidal, Alicia Llorente, Fina Climent, Alex Cordero, Idoia Morilla, Maria Molina-Molina, A Guma, Miriam Campos, Manel Esteller, Miguel Angel Pujana, Laia Gómez-Baldó, Gorka Ruiz de Garibay, Adela Fernandez, Javier Hernández-Losa, José I. López, Roger Llatjós, Nadia García, Claudia Valenzuela, Ana I. Extremera, Jacopo Boni, Carmen Herranz, Miguel Gil, Eva González-Suárez, Helena Aguilar, Sonia Pernas
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Addi. Archivo Digital para la Docencia y la Investigación
PLoS ONE
Dipòsit Digital de la UB
Universidad de Barcelona
PLoS ONE, Vol 10, Iss 7, p e0132546 (2015)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
instname
Addi. Archivo Digital para la Docencia y la Investigación
PLoS ONE
Dipòsit Digital de la UB
Universidad de Barcelona
PLoS ONE, Vol 10, Iss 7, p e0132546 (2015)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Lymphangioleiomyomatosis (LAM) is a rare lung-metastasizing neoplasm caused by the proliferation of smooth muscle-like cells that commonly carry loss-of-function mutations in either the tuberous sclerosis complex 1 or 2 (TSC1 or TSC2) genes. While al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1da74b006cf1634867ee9d356219f78
http://hdl.handle.net/2445/69339
http://hdl.handle.net/2445/69339
- [1]
- « Předchozí
- 1
- 2