Zobrazeno 1 - 10
of 141
pro vyhledávání: '"Ana, Peixoto"'
Autor:
Maria P. Silva, Luísa T. Ferreira, Natércia F. Brás, Lurdes Torres, Andreia Brandão, Manuela Pinheiro, Marta Cardoso, Adriana Resende, Joana Vieira, Carlos Palmeira, Gabriela Martins, Miguel Silva, Carla Pinto, Ana Peixoto, João Silva, Rui Henrique, Sofia Maia, Helder Maiato, Manuel R. Teixeira, Paula Paulo
Publikováno v:
Journal of Biomedical Science, Vol 31, Iss 1, Pp 1-17 (2024)
Abstract Background Prostate cancer (PrCa) is the most frequently diagnosed cancer in men. Variants in known moderate- to high-penetrance genes explain less than 5% of the cases arising at early-onset (
Externí odkaz:
https://doaj.org/article/89556ac24efa46d1a230f329bd5bf87d
Autor:
Ana Peixoto, Luís Cirnes, Ana Luísa Carvalho, Maria João Andrade, Maria José Brito, Paula Borralho, Nuno Coimbra, Pedro M. Borralho, Ana Sofia Carneiro, Lisandra Castro, Lurdes Correia, Maria Rita Dionísio, Carlos Faria, Paulo Figueiredo, Ana Gomes, Joana Paixão, Manuela Pinheiro, Hugo Prazeres, Joana Ribeiro, Natália Salgueiro, Fernando. C Schmitt, Fátima Silva, Ana Rita Silvestre, Ana Carla Sousa, Joana Almeida-Tavares, Manuel R. Teixeira, Saudade André, Jose Carlos Machado
Publikováno v:
Frontiers in Molecular Biosciences, Vol 11 (2024)
Externí odkaz:
https://doaj.org/article/773bd9c47bef4a62ab1e4d2e430b1cd2
Autor:
Ana Peixoto
Publikováno v:
Acta Médica Portuguesa, Vol 37, Iss 2 (2024)
N/D.
Externí odkaz:
https://doaj.org/article/94c313f5d18241f8b8f2b8c6edb7a636
Autor:
Carla Pinto, Joana Guerra, Manuela Pinheiro, Carla Escudeiro, Catarina Santos, Pedro Pinto, Miguel Porto, Carla Bartosch, João Silva, Ana Peixoto, Manuel R. Teixeira
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
NTHL1 tumor syndrome is an autosomal recessive rare disease caused by biallelic inactivating variants in the NTHL1 gene and which presents a broad tumor spectrum. To contribute to the characterization of the phenotype of this syndrome, we studied 467
Externí odkaz:
https://doaj.org/article/16c7d05f7ba64b5ca00892e14af04742
Autor:
Guillaume Albouy, Jared Barron, Hugues Beauchesne, Elias Bernreuther, Marcella Bona, Cesare Cazzaniga, Cari Cesarotti, Timothy Cohen, Annapaola de Cosa, David Curtin, Zeynep Demiragli, Caterina Doglioni, Alison Elliot, Karri Folan DiPetrillo, Florian Eble, Carlos Erice, Chad Freer, Aran Garcia-Bellido, Caleb Gemmell, Marie-Hélène Genest, Giovanni Grilli di Cortona, Giuliano Gustavino, Nicoline Hemme, Tova Holmes, Deepak Kar, Simon Knapen, Suchita Kulkarni, Luca Lavezzo, Steven Lowette, Benedikt Maier, Seán Mee, Stephen Mrenna, Harikrishnan Nair, Jeremi Niedziela, Christos Papageorgakis, Nukulsinh Parmar, Christoph Paus, Kevin Pedro, Ana Peixoto, Alexx Perloff, Tilman Plehn, Christiane Scherb, Pedro Schwaller, Jessie Shelton, Akanksha Singh, Sukanya Sinha, Torbjörn Sjöstrand, Aris G. B. Spourdalakis, Daniel Stolarski, Matthew J. Strassler, Andrii Usachov, Carlos Vázquez Sierra, Christopher B. Verhaaren, Long Wang
Publikováno v:
European Physical Journal C: Particles and Fields, Vol 82, Iss 12, Pp 1-66 (2022)
Abstract In this work, we consider the case of a strongly coupled dark/hidden sector, which extends the Standard Model (SM) by adding an additional non-Abelian gauge group. These extensions generally contain matter fields, much like the SM quarks, an
Externí odkaz:
https://doaj.org/article/f1039d0e73de43e7877021a3c7e40dd2
Autor:
Christopher Hakkaart, John F. Pearson, Louise Marquart, Joe Dennis, George A. R. Wiggins, Daniel R. Barnes, Bridget A. Robinson, Peter D. Mace, Kristiina Aittomäki, Irene L. Andrulis, Banu K. Arun, Jacopo Azzollini, Judith Balmaña, Rosa B. Barkardottir, Sami Belhadj, Lieke Berger, Marinus J. Blok, Susanne E. Boonen, Julika Borde, Angela R. Bradbury, Joan Brunet, Saundra S. Buys, Maria A. Caligo, Ian Campbell, Wendy K. Chung, Kathleen B. M. Claes, GEMO Study Collaborators, EMBRACE Collaborators, Marie-Agnès Collonge-Rame, Jackie Cook, Casey Cosgrove, Fergus J. Couch, Mary B. Daly, Sita Dandiker, Rosemarie Davidson, Miguel de la Hoya, Robin de Putter, Capucine Delnatte, Mallika Dhawan, Orland Diez, Yuan Chun Ding, Susan M. Domchek, Alan Donaldson, Jacqueline Eason, Douglas F. Easton, Hans Ehrencrona, Christoph Engel, D. Gareth Evans, Ulrike Faust, Lidia Feliubadaló, Florentia Fostira, Eitan Friedman, Megan Frone, Debra Frost, Judy Garber, Simon A. Gayther, Andrea Gehrig, Paul Gesta, Andrew K. Godwin, David E. Goldgar, Mark H. Greene, Eric Hahnen, Christopher R. Hake, Ute Hamann, Thomas V. O. Hansen, Jan Hauke, Julia Hentschel, Natalie Herold, Ellen Honisch, Peter J. Hulick, Evgeny N. Imyanitov, SWE-BRCA Investigators, kConFab Investigators, HEBON Investigators, Claudine Isaacs, Louise Izatt, Angel Izquierdo, Anna Jakubowska, Paul A. James, Ramunas Janavicius, Esther M. John, Vijai Joseph, Beth Y. Karlan, Zoe Kemp, Judy Kirk, Irene Konstantopoulou, Marco Koudijs, Ava Kwong, Yael Laitman, Fiona Lalloo, Christine Lasset, Charlotte Lautrup, Conxi Lazaro, Clémentine Legrand, Goska Leslie, Fabienne Lesueur, Phuong L. Mai, Siranoush Manoukian, Véronique Mari, John W. M. Martens, Lesley McGuffog, Noura Mebirouk, Alfons Meindl, Austin Miller, Marco Montagna, Lidia Moserle, Emmanuelle Mouret-Fourme, Hannah Musgrave, Sophie Nambot, Katherine L. Nathanson, Susan L. Neuhausen, Heli Nevanlinna, Joanne Ngeow Yuen Yie, Tu Nguyen-Dumont, Liene Nikitina-Zake, Kenneth Offit, Edith Olah, Olufunmilayo I. Olopade, Ana Osorio, Claus-Eric Ott, Sue K. Park, Michael T. Parsons, Inge Sokilde Pedersen, Ana Peixoto, Pedro Perez-Segura, Paolo Peterlongo, Timea Pocza, Paolo Radice, Juliane Ramser, Johanna Rantala, Gustavo C. Rodriguez, Karina Rønlund, Efraim H. Rosenberg, Maria Rossing, Rita K. Schmutzler, Payal D. Shah, Saba Sharif, Priyanka Sharma, Lucy E. Side, Jacques Simard, Christian F. Singer, Katie Snape, Doris Steinemann, Dominique Stoppa-Lyonnet, Christian Sutter, Yen Yen Tan, Manuel R. Teixeira, Soo Hwang Teo, Mads Thomassen, Darcy L. Thull, Marc Tischkowitz, Amanda E. Toland, Alison H. Trainer, Vishakha Tripathi, Nadine Tung, Klaartje van Engelen, Elizabeth J. van Rensburg, Ana Vega, Alessandra Viel, Lisa Walker, Jeffrey N. Weitzel, Marike R. Wevers, Georgia Chenevix-Trench, Amanda B. Spurdle, Antonis C. Antoniou, Logan C. Walker
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-15 (2022)
The risk of germline copy number variants (CNVs) in BRCA1 and BRCA2 pathogenic variant carriers in breast cancer is assessed, with CNVs overlapping SULT1A1 decreasing breast cancer risk in BRCA1 carriers.
Externí odkaz:
https://doaj.org/article/2008d12983b5437282b0bdff8c8a6bb0
Autor:
Ana Peixoto, Luís Cirnes, Ana Luísa Carvalho, Maria João Andrade, Maria José Brito, Paula Borralho, Nuno Coimbra, Pedro M. Borralho, Ana Sofia Carneiro, Lisandra Castro, Lurdes Correia, Maria Rita Dionísio, Carlos Faria, Paulo Figueiredo, Ana Gomes, Joana Paixão, Manuela Pinheiro, Hugo Prazeres, Joana Ribeiro, Natália Salgueiro, Fernando C. Schmitt, Fátima Silva, Ana Rita Silvestre, Ana Carla Sousa, Joana Almeida-Tavares, Manuel R. Teixeira, Saudade André, José Carlos Machado
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Background: Around 40% of ER+/HER2-breast carcinomas (BC) present mutations in the PIK3CA gene. Assessment of PIK3CA mutational status is required to identify patients eligible for treatment with PI3Kα inhibitors, with alpelisib currently the only a
Externí odkaz:
https://doaj.org/article/743caa08d4a54bebaf8dab1e985c14bc
Autor:
Fernanda Silva, Filipa Coelho, Ana Peixoto, Pedro Pinto, Carmo Martins, Ann-Sophie Frombach, Vítor E. Santo, Catarina Brito, António Guimarães, Ana Félix
Publikováno v:
Cancer Cell International, Vol 22, Iss 1, Pp 1-17 (2022)
Highlights IPOLFG-SOC43 cell line represents the heterogeneity of Epithelial Ovarian Cancer Genetic alterations in cancer cells confer a selective advantage 3D cultures preserve the phenotypical features of the original tumor
Externí odkaz:
https://doaj.org/article/71cd59d565b44b1b83724cd94dc06196
Publikováno v:
Revista Portuguesa de Psiquiatria e Saúde Mental, Vol 8, Iss 2 (2022)
Intimate partner violence (IPV) perpetrated by men is a highly prevalent public health problem. IPV has long been asso- ciated to substance use disorder (SUD) in young women, namely alcohol-related problems. However, evidence on this link regarding l
Externí odkaz:
https://doaj.org/article/46f75dc78dc1472ba63ac4d6e38efeff
Publikováno v:
Journal of High Energy Physics, Vol 2020, Iss 10, Pp 1-23 (2020)
Externí odkaz:
https://doaj.org/article/8c286b34399146fdaddf06e0e053d8fc