Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Silvia Vidal-Millan"'
Autor:
Silvia Vidal-Millan, Zyanya Lucia Zatarain-Barrón, Kena Daza-Galicia, Daniela Shveid Gerson, Pavel Salvador Pichardo-Rojas, Alejandro Salazar-Pigeon, Talia Wegman-Ostrosky
Publikováno v:
Frontiers in Oncology, Vol 13 (2024)
PurposeNeurofibromatosis type 1 (NF1) is a complex, multisystem disorder that is characterized, among other features, by a higher risk of developing benign and malignant tumors. Despite NF1 being one of the most common autosomal dominant genetic diso
Externí odkaz:
https://doaj.org/article/b1e75f7c57d848a1be6e5c8cd98af526
Autor:
Felipe Vaca-Paniagua, Rosa María Alvarez-Gomez, Verónica Fragoso-Ontiveros, Silvia Vidal-Millan, Luis Alonso Herrera, David Cantú, Enrique Bargallo-Rocha, Alejandro Mohar, César López-Camarillo, Carlos Pérez-Plasencia
Publikováno v:
PLoS ONE, Vol 7, Iss 5, p e37432 (2012)
Hereditary breast cancer comprises 10% of all breast cancers. The most prevalent genes causing this pathology are BRCA1 and BRCA2 (breast cancer early onset 1 and 2), which also predispose to other cancers. Despite the outstanding relevance of geneti
Externí odkaz:
https://doaj.org/article/2c5d0369768842878eb1296cfc2a54a6
Autor:
Enrique Soto-Pérez-de-Celis, Dione Aguilar-y-Méndez, Silvia R. Allende-Pérez, Rosa Ma. Álvarez-Gómez, Verónica Cedillo-Compeán, Ma. Teresa de J. Cervantes-Díaz, Mariana Chávez-MacGregor, Mabelid Mabiani-Céspedes, Edith A. Monreal-Carrillo, Ma. Paulina Núñez-Martínez, Guadalupe E. Paredes-Rivera, Edith Rojas-Castillo, Sofía Saba-Cohén, Isabelle A. Timeus-Salvato, Emma L. Verastegui-Avilés, Silvia Vidal-Millán, Talia Wegman-Ostrosky, Claudia Arce-Salinas, Juan E. Bargalló-Rocha, Verónica Bautista-Piña, Guadalupe Cervantes-Sánchez, Christian H. Flores-Balcázar, Ma. del Carmen Lara-Tamburrino, Ana Lluch-Hernández, Antonio Maffuz-Aziz, Víctor M. Pérez-Sánchez, Adela Poitevin-Chacón, Efraín Salas-González, Laura Torrecillas-Torres, Vicente Valero-Castillo, Yolanda Villaseñor-Navarro, Jesús Cárdenas-Sánchez
Publikováno v:
Gaceta Mexicana de Oncología, Vol 23, Iss 3 (2024)
El cáncer mamario impacta en diversas esferas de la vida del paciente y su entorno familiar y social. Se trata de una enfermedad compleja que requiere un abordaje multidisciplinario tanto para el diagnóstico como para el tratamiento, así como en l
Externí odkaz:
https://doaj.org/article/640c35456c5c41e08568b6fdb27c3e18
Autor:
Julieta Dominguez-Ortiz, Rosa M. Álvarez-Gómez, Rogelio Montiel-Manríquez, Alberto Cedro-Tanda, Nicolás Alcaraz, Clementina Castro-Hernández, Luis Bautista-Hinojosa, Laura Contreras-Espinosa, Leda Torres-Maldonado, Verónica Fragoso-Ontiveros, Yuliana Sánchez-Contreras, Rodrigo González-Barrios, Marcela Angélica De la Fuente-Hernández, María de la Luz Mejía-Aguayo, Ulises Juárez-Figueroa, Alejandra Padua-Bracho, Rodrigo Sosa-León, Gabriela Obregon-Serrano, Silvia Vidal-Millán, Paulina María Núñez-Martínez, Abraham Pedroza-Torres, Sergio Nicasio-Arzeta, Alfredo Rodríguez, Fernando Luna, Fernanda Cisneros-Soberanis, Sara Frías, Cristian Arriaga-Canon, Luis A. Herrera-Montalvo
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 12, p 6773 (2024)
Hereditary breast and ovarian cancer (HBOC) syndrome is a genetic condition that increases the risk of breast cancer by 80% and that of ovarian cancer by 40%. The most common pathogenic variants (PVs) causing HBOC occur in the BRCA1 gene, with more t
Externí odkaz:
https://doaj.org/article/63f3b50e5ad24d0bb3e2d341782421ea
Autor:
Paulina M. Núñez-Martínez, Lucía Taja-Chayeb, Miguel A. Ramírez-Otero, Verónica Fragoso-Ontiveros, Talia Wegman-Ostrosky, David Cruz-Robles, Silvia Vidal-Millán
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 78, Iss 4 (2021)
Background: Patients with familial erythrocytosis type 2 have no increased risk of von Hippel-Lindau-associated tumors, although mutations in the VHL gene cause both pathologies. Case report: We present a case of a compound heterozygote patient with
Externí odkaz:
https://doaj.org/article/752b3cf6bd0c433d9cc0817b7dbcbd1f
Autor:
Alejandra Padua-Bracho, José A. Velázquez-Aragón, Verónica Fragoso-Ontiveros, Paulina María Nuñez-Martínez, María de la Luz Mejía Aguayo, Yuliana Sánchez-Contreras, Miguel Angel Ramirez-Otero, Marcela Angélica De la Fuente-Hernández, Silvia Vidal-Millán, Talia Wegman-Ostrosky, Abraham Pedroza-Torres, Cristian Arriaga-Canon, Luis A. Herrera-Montalvo, Rosa Maria Alvarez-Gómez
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11549 (2022)
Lynch syndrome (LS) is the main hereditary colorectal cancer syndrome. There have been few reports regarding the clinical and molecular characteristics of LS patients in Latin America; this is particularly true in the Mexican population, where no inf
Externí odkaz:
https://doaj.org/article/d9fcd9d698364107b20778b579eb874f
Autor:
Veronica Fragoso-Ontiveros, Jose Antonio Velázquez-Aragón, Paulina Maria Nuñez-Martínez, Maria de la Luz Mejía-Aguayo, Silvia Vidal-Millán, Abraham Pedroza-Torres, Yuliana Sánchez-Contreras, Miguel Angel Ramírez-Otero, Rodolfo Muñiz-Mendoza, Julieta Domínguez-Ortíz, Talia Wegman-Ostrosky, Juan Enrique Bargalló-Rocha, Dolores Gallardo-Rincón, Nancy Reynoso-Noveron, Cristian Arriaga-Canon, Abelardo Meneses-García, Luis Alonso Herrera-Montalvo, Rosa Maria Alvarez-Gomez
Publikováno v:
PLoS ONE, Vol 14, Iss 9, p e0222709 (2019)
The deletion of exons 9 to 12 of BRCA1 (9-12 del BRCA1) is considered a founder mutation in the Mexican population. We evaluate the usefulness of the target detection of 9-12 del BRCA1 as the first molecular diagnostic strategy in patients with Hered
Externí odkaz:
https://doaj.org/article/ba874e765f07415ab0f764e90549aecb
Autor:
Alexander Perdomo-Pantoja, Sonia Iliana Mejía-Pérez, Nancy Reynoso-Noverón, Liliana Gómez-Flores-Ramos, Ernesto Soto-Reyes, Thalía Estefania Sánchez-Correa, Lissania Guerra-Calderas, Clementina Castro-Hernandez, Silvia Vidal-Millán, José Sánchez-Corona, Lucia Taja-Chayeb, Olga Gutiérrez, Bernardo Cacho-Diaz, Rosa Maria Alvarez-Gomez, Juan Luis Gómez-Amador, Patricia Ostrosky-Wegman, Teresa Corona, Luis Alonso Herrera-Montalvo, Talia Wegman-Ostrosky
Publikováno v:
PLoS ONE, Vol 13, Iss 11, p e0206590 (2018)
INTRODUCTION:Renin-angiotensin system (RAS) in brain cancer represents a scarcely explored field in neuro-oncology. Recently, some pre- and clinical studies have reported that RAS components play a relevant role in the development and behavior of gli
Externí odkaz:
https://doaj.org/article/48b561468849485c963486e8ba299804
Autor:
Lucia Taja Chayeb, Olga Gutierrez Hernandez, Silvia Vidal Millan, Vanessa Rosas Camargo, Alfonso Dueñas-González
Publikováno v:
BMC Cancer, Vol 7, Iss Suppl 1, p A5 (2007)
BMC Cancer
BMC Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1da066df1a2042ebe8f518ea8e54e197