Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Sara, Larriba"'
Autor:
Adriana Ferre-Giraldo, Manel Castells, José Francisco Sánchez-Herrero, Olga López-Rodrigo, Maurizio de Rocco-Ponce, Lluís Bassas, Francesc Vigués, Lauro Sumoy, Sara Larriba
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 18, p 10122 (2024)
PSA screening has led to an over-diagnosis of prostate cancer (PCa) and unnecessary biopsies of benign conditions due to its low cancer specificity. Consequently, more accurate, preferentially non-invasive, tests are needed. We aim to evaluate the po
Externí odkaz:
https://doaj.org/article/1024b2e8cc624e3fa198ce62d2dcac76
Autor:
Miriam Cerván-Martín, Frank Tüttelmann, Alexandra M. Lopes, Lara Bossini-Castillo, Rocío Rivera-Egea, Nicolás Garrido, Saturnino Lujan, Gema Romeu, Samuel Santos-Ribeiro, José A. Castilla, M. Carmen Gonzalvo, Ana Clavero, Vicente Maldonado, F. Javier Vicente, Sara González-Muñoz, Andrea Guzmán-Jiménez, Miguel Burgos, Rafael Jiménez, Alberto Pacheco, Cristina González, Susana Gómez, David Amorós, Jesus Aguilar, Fernando Quintana, Carlos Calhaz-Jorge, Ana Aguiar, Joaquim Nunes, Sandra Sousa, Isabel Pereira, Maria Graça Pinto, Sónia Correia, Josvany Sánchez-Curbelo, Olga López-Rodrigo, Javier Martín, Iris Pereira-Caetano, Patricia I. Marques, Filipa Carvalho, Alberto Barros, Jörg Gromoll, Lluís Bassas, Susana Seixas, João Gonçalves, Sara Larriba, Sabine Kliesch, Rogelio J. Palomino-Morales, F. David Carmona
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-13 (2022)
A GWAS in a large case-control cohort of European ancestry identifies two genomic regions, the MHC class II gene HLA-DRB1 and an upstream locus of VRK1, that are associated with the most severe phenotype of spermatogenic failure.
Externí odkaz:
https://doaj.org/article/77b3fe3532a14229aef1e788bb1d7f9d
Autor:
Adriana Ferre, Lucía Santiago, José Francisco Sánchez-Herrero, Olga López-Rodrigo, Josvany Sánchez-Curbelo, Lauro Sumoy, Lluís Bassas, Sara Larriba
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 20, p 15436 (2023)
Small RNA-sequencing (small RNA-seq) has revealed the presence of small RNA-naturally occurring variants such as microRNA (miRNA) isoforms or isomiRs. Due to their small size and the sequence similarity among miRNA isoforms, their validation by RT-qP
Externí odkaz:
https://doaj.org/article/c17865f9d64e4cdb8920ea9e4f434f10
Autor:
Andrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, Rocío Rivera-Egea, Nicolás Garrido, Saturnino Luján, Samuel Santos-Ribeiro, José A. Castilla, M. Carmen Gonzalvo, Ana Clavero, F. Javier Vicente, Vicente Maldonado, Javier Villegas-Salmerón, Miguel Burgos, Rafael Jiménez, Maria Graça Pinto, Isabel Pereira, Joaquim Nunes, Josvany Sánchez-Curbelo, Olga López-Rodrigo, Iris Pereira-Caetano, Patricia Isabel Marques, Filipa Carvalho, Alberto Barros, Lluís Bassas, Susana Seixas, João Gonçalves, Alexandra M. Lopes, Sara Larriba, Rogelio J. Palomino-Morales, F. David Carmona, Lara Bossini-Castillo, IVIRMA Group, Lisbon Clinical Group
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 10 (2022)
Background: Severe spermatogenic failure (SPGF) represents one of the most relevant causes of male infertility. This pathological condition can lead to extreme abnormalities in the seminal sperm count, such as severe oligozoospermia (SO) or non-obstr
Externí odkaz:
https://doaj.org/article/888486e3bcaf4088a22f990d7ff53f24
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 6, p 5447 (2023)
Reproductive dysfunction and urogenital malignancies represent a serious health concern in men. This is in part as a result of the absence of reliable non-invasive tests of diagnosis/prognosis. Optimizing diagnosis and predicting the patient’s prog
Externí odkaz:
https://doaj.org/article/19b7747f7aae4515a3a4d6c620b9231e
Autor:
Miriam Cerván-Martín, Lara Bossini-Castillo, Andrea Guzmán-Jimenez, Rocío Rivera-Egea, Nicolás Garrido, Saturnino Luján, Gema Romeu, Samuel Santos-Ribeiro, IVIRMA Group, Lisbon Clinical Group, José A. Castilla, M. Carmen Gonzalvo, Ana Clavero, F. Javier Vicente, Vicente Maldonado, Sara González-Muñoz, Inmaculada Rodríguez-Martín, Miguel Burgos, Rafael Jiménez, Maria Graça Pinto, Isabel Pereira, Joaquim Nunes, Josvany Sánchez-Curbelo, Olga López-Rodrigo, Iris Pereira-Caetano, Patricia Isabel Marques, Filipa Carvalho, Alberto Barros, Lluís Bassas, Susana Seixas, João Gonçalves, Sara Larriba, Alexandra M. Lopes, F. David Carmona, Rogelio J. Palomino-Morales
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 6, p 932 (2022)
We aimed to analyze the role of the common genetic variants located in the PIN1 locus, a relevant prolyl isomerase required to control the proliferation of spermatogonial stem cells and the integrity of the blood–testis barrier, in the genetic risk
Externí odkaz:
https://doaj.org/article/7a24ea05e5c342a682a99a88c7c0494e
Publikováno v:
Andrology
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Dipòsit Digital de la UB
Universidad de Barcelona
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Background and objectives Predicting the origin of azoospermia with non-invasive biomarkers is clinically relevant for determining the chance of successful sperm retrieval from the testes before attempting assisted reproduction treatment. Here, the s
Publikováno v:
Reproductive BioMedicine Online. 45:332-340
Would the use of genome-wide genotyping be an advantageous strategy to identify the molecular aetiology of two brothers from a non-consanguineous family, clinically diagnosed with total globozoospermia?Two related Spanish globozoospermic patients wer
Autor:
Sara Larriba, Jose Francisco Sánchez‐Herrero, Raquel Pluvinet, Olga López‐Rodrigo, Lluís Bassas, Lauro Sumoy
Publikováno v:
Andrology.
Autor:
Miriam Cerván-Martín, Lara Bossini-Castillo, Rocío Rivera-Egea, Nicolás Garrido, Saturnino Luján, Gema Romeu, Samuel Santos-Ribeiro, IVIRMA Group, Lisbon Clinical Group, José A. Castilla, M. Carmen Gonzalvo, Ana Clavero, F. Javier Vicente, Andrea Guzmán-Jiménez, Cláudia Costa, Inés Llinares-Burguet, Chiranan Khantham, Miguel Burgos, Francisco J. Barrionuevo, Rafael Jiménez, Josvany Sánchez-Curbelo, Olga López-Rodrigo, M. Fernanda Peraza, Iris Pereira-Caetano, Patricia I. Marques, Filipa Carvalho, Alberto Barros, Lluís Bassas, Susana Seixas, João Gonçalves, Sara Larriba, Alexandra M. Lopes, Rogelio J. Palomino-Morales, F. David Carmona
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 1, p 22 (2020)
Infertility is a growing concern in developed societies. Two extreme phenotypes of male infertility are non-obstructive azoospermia (NOA) and severe oligospermia (SO), which are characterized by severe spermatogenic failure (SpF). We designed a genet
Externí odkaz:
https://doaj.org/article/fd7d40a1efd048c4a5f1825a040635eb