Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Josep Maria Estanyol"'
Autor:
Judit Castillo, Orleigh Adeleccia Bogle, Meritxell Jodar, Forough Torabi, David Delgado-Dueñas, Josep Maria Estanyol, Josep Lluís Ballescà, David Miller, Rafael Oliva
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
The male gamete is not completely mature after ejaculation and requires further events in the female genital tract to acquire fertilizing ability, including the processes of capacitation and acrosome reaction. In order to shed light on protein change
Externí odkaz:
https://doaj.org/article/6d47959ef6e349d9a01fb89d5566c352
Publikováno v:
Asian Journal of Andrology, Vol 17, Iss 4, Pp 601-609 (2015)
The classical idea about the function of the mammalian sperm chromatin is that it serves to transmit a highly protected and transcriptionally inactive paternal genome, largely condensed by protamines, to the next generation. In addition, recent sperm
Externí odkaz:
https://doaj.org/article/aa4b713672d34d2ab981cb5cdf649b83
Autor:
Judit Castillo, Rafael Oliva, Meritxell Jodar, Dafni Anastasiadi, Francesc Piferrer, Josep Maria Estanyol, Ferran Barrachina
Publikováno v:
XIIIth International Symposium on Spermatology ISBN: 9783030662912
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
XIII International Symposium on Spermatology, 9-13 May 2018, Stockholm, Sweden
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::006ef6f0c6fd7f71efeeff1d1df409c0
https://doi.org/10.1007/978-3-030-66292-9_9
https://doi.org/10.1007/978-3-030-66292-9_9
Autor:
Neus Agell, Gabriel Capellá, Carles Barceló, Baraa Abuasaker, Noelia Paco, Sonia Brun, Josep Maria Estanyol, Mireia M. Ginestà, Debora Cabot, Núria Gendrau-Sanclemente, Carles Rentero, Triana Ruiz-Fariña, Gabriel Pons, Montserrat Jaumot, Marta Bosch, Miriam Cuatrecasas
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Universidad de Barcelona
Oncogenic mutations of KRAS are found in the most aggressive human tumors, including colorectal cancer. It has been suggested that oncogenic KRAS phosphorylation at Ser181 modulates its activity and favors cell transformation. Using nonphosphorylatab
Autor:
Pedro de la Villa, Jordi Andilla, Josep Maria Estanyol, María José Fidalgo, Anna Plana-Bonamaisó, Ana Mendez, Santiago López-Begines, Pablo Loza-Alvarez
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Cell Death and Disease, Vol 11, Iss 1, Pp 1-19 (2020)
Cell Death & Disease
Universidad de Barcelona
Cell Death and Disease, Vol 11, Iss 1, Pp 1-19 (2020)
Cell Death & Disease
Loss-of-function mutations in the retinal degeneration 3 (RD3) gene cause inherited retinopathy with impaired rod and cone function and fast retinal degeneration in patients and in the natural strain of rd3 mice. The underlying physiopathology mechan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0262347563627c263818dddafa446f
http://hdl.handle.net/2445/173327
http://hdl.handle.net/2445/173327
Autor:
Jezid Miranda, L. Youssef, Cristina Paules, Guerau Fernandez, Francesca Crovetto, Josep Maria Estanyol, Eduard Gratacós, Fatima Crispi
Publikováno v:
Zaguán: Repositorio Digital de la Universidad de Zaragoza
Universidad de Zaragoza
Scientific Reports
SCIENTIFIC REPORTS
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Zaguán. Repositorio Digital de la Universidad de Zaragoza
Consejo Superior de Investigaciones Científicas (CSIC)
Universidad de Zaragoza
Scientific Reports
SCIENTIFIC REPORTS
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Zaguán. Repositorio Digital de la Universidad de Zaragoza
Consejo Superior de Investigaciones Científicas (CSIC)
Fetal growth restriction defined as the failure to achieve the fetal genetic growth potential is a major cause of perinatal morbidity and mortality. The role of maternal adaptations to placental insufficiency in this disorder is still not fully under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d6b250ecef1582b4ec0441311223018
http://zaguan.unizar.es/record/97394
http://zaguan.unizar.es/record/97394
Publikováno v:
MHR: Basic science of reproductive medicine. 23:803-816
STUDY QUESTION\ud \ud \ud \ud Are there novel hyaladherins in human sperm?\ud \ud \ud \ud SUMMARY ANSWER\ud \ud \ud \ud Zona pellucida-binding protein 2 (ZPBP2), containing a Link-like hyaluronic acid (HA)-binding domain, and several other proteins c
Autor:
Carme Mallofré, Josep Maria Estanyol, Ferran Barrachina, Meritxell Jodar, Rafael Oliva, David Delgado-Dueñas, Josep Lluís Ballescà, Ada Soler-Ventura
Publikováno v:
Molecularcellular proteomics : MCP. 18(Suppl 1)
Our aim was to define seminal plasma proteome signatures of infertile patients categorized according to their seminal parameters using TMT-LC-MS/MS. To that extent, quantitative proteomic data was analyzed following two complementary strategies: (1)
Autor:
Erwin Knecht, Martina Guerrero-Hernández, Carmen Aguado, Judit Macías-Vidal, Maria Josep Coll, Oriol Bachs, Josep Maria Estanyol
Publikováno v:
PROTEOMICS
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
Niemann-Pick type C (NPC) disease is an inherited lysosomal storage disorder, characterized by severe neurodegeneration. It is mostly produced by mutations in the NPC1 gene, encoding for a protein of the late endosomes/lysosomes membrane, involved in
Autor:
Ferran Barrachina, Francesc Piferrer, Dafni Anastasiadi, Judit Castillo, Meritxell Jodar, Josep Maria Estanyol, Rafael Oliva
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Special issue in Honor of Gordon H. Dixon.-- 16 pages, supplemental material https://www.tandfonline.com/doi/suppl/10.1080/19396368.2018.1482383?scroll=top
A very common conception about the function of the spermatozoon is that its unique role i
A very common conception about the function of the spermatozoon is that its unique role i