Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Patricia Pérez-Vera"'
Autor:
Emiy Yokoyama, Camilo E. Villarroel, Sinhué Diaz, Victoria Del Castillo, Patricia Pérez-Vera, Consuelo Salas, Samuel Gómez, Reneé Barreda, Bertha Molina, Sara Frias
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-7 (2020)
Abstract Background Monosomy of 1p36 is considered the most common terminal microdeletion syndrome. It is characterized by intellectual disability, growth retardation, seizures, congenital anomalies, and distinctive facial features that are absent wh
Externí odkaz:
https://doaj.org/article/7eee9280a0c74043b0f443ab5f12114a
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 74, Iss 4, Pp 243-264 (2017)
La leucemia linfoblástica aguda (LLA) es el tipo de cáncer más frecuente en niños. Aunque se sabe que las alteraciones genéticas constituyen la base de la etiología de la LLA, se ha demostrado que no son suficientes para el desarrollo leucémic
Externí odkaz:
https://doaj.org/article/aa336d410c9c4491b1d5ee8469fa48b5
Autor:
Adriana Reyes-León, Rocío Juárez-Velázquez, Alma Medrano-Hernández, Teresa Cuenca-Roldán, Consuelo Salas-Labadía, María Del Pilar Navarrete-Meneses, Roberto Rivera-Luna, Gerardo López-Hernández, Rogelio Paredes-Aguilera, Patricia Pérez-Vera
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0130756 (2015)
Expression of the 6 and 8 dominant-negative Ikaros isoforms in pediatric patients with acute lymphoblastic leukemia has been associated with a high risk of relapse and death; due to these isoforms disrupting the differentiation and proliferation of l
Externí odkaz:
https://doaj.org/article/5188c281d31e406ba02d2fd757231cab
Autor:
Daniel Martínez Anaya, María del Rocío Juárez-Velázquez, Sinuhé Reyes Ruvalcaba, María del Pilar Navarrete-Meneses, Consuelo Salas Labadía, Esther Lieberman Hernández, Patricia Pérez-Vera
Publikováno v:
Molecular Syndromology. :1-12
Introduction: The pure interstitial trisomy 11q11q23.2 is an uncommon genomic disorder associated with nonrecurrent intrachromosomal duplications. The phenotype is characterized by intellectual disability and craniofacial abnormalities. Given their u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6e420a7626b310d8ecaf1db104818ca
https://doi.org/10.1159/000528472
https://doi.org/10.1159/000528472
Autor:
Daniel Martínez-Anaya, Dafné Moreno-Lorenzana, Adriana Reyes-León, Ulises Juárez-Figueroa, Michael Dean, María Montserrat Aguilar-Hernández, Netzi Rivera-Sánchez, Jessica García-Islas, Victoria Vieyra-Fuentes, Marta Zapata-Tarrés, Luis Juárez-Villegas, Rogelio Paredes-Aguilera, Lourdes Vega-Vega, Roberto Rivera-Luna, María del Rocío Juárez-Velázquez, Patricia Pérez-Vera
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 17; Pages: 9587
Ph-like subtypes with CRLF2 abnormalities are frequent among Hispano–Latino children with pre-B ALL. Therefore, there is solid ground to suggest that this subtype is frequent in Mexican patients. The genomic complexity of Ph-like subtype constitute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3711664631e1f0ac152c0ea4132f4da
Autor:
Rogelio Paredes Aguilera, Dafné Moreno Lorenzana, Marta Zapata Tarrés, Consuelo Salas Labadía, Adriana Reyes León, Daniel Martínez Anaya, Luis Enrique Juárez Villegas, María Del Pilar Navarrete Meneses, Rocío Cárdenas Cardós, Martha Herrera Almanza, María Del Rocío Juárez Velázquez, Berenice Jarquín Ramírez, Patricia Pérez Vera, Adrián Hernández Monterde
Publikováno v:
The Journal of Pathology: Clinical Research. 7:410-421
The gene fusions BCR-ABL1, TCF3-PBX1, and ETV6-RUNX1 are recurrent in B-cell acute lymphoblastic leukemia (B-ALL) and are found with low frequency in coexistence with CRLF2 (cytokine receptor-like factor 2) rearrangements and overexpression. There is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab0f70c3c8f0c0acd37ed4e4aefeece2
https://doi.org/10.1002/cjp2.211
https://doi.org/10.1002/cjp2.211
Autor:
María del Pilar Navarrete-Meneses, Consuelo Salas-Labadía, María del Rocío Juárez-Velázquez, Dafné Moreno-Lorenzana, Fernando Gómez-Chávez, Alberto Olaya-Vargas, Patricia Pérez-Vera
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 7; Pages: 6259
The evidence supporting the biological plausibility of the association of permethrin and malathion with hematological cancer is limited and contradictory; thus, further studies are needed. This study aimed to investigate whether in vitro exposure to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a24dced5b37d33f688e2ee212a5c87ae
https://doi.org/10.3390/ijms24076259
https://doi.org/10.3390/ijms24076259
Autor:
Paola Alejandra Romecin, Patricia Pérez-Vera, Meritxell Vinyoles, Anna Bigas, Eric Kowarz, Clara Bueno, Pedro J. Marín, Virginia C Rodriguez-Cortez, Jessica González, Carlos Gómez-Marín, Talia Velasco-Hernandez, Felipe Cortes-Ledesma, Andrea Terron, Pablo Menendez, María del Pilar Navarrete-Meneses, Oscar Molina, Francisco Gutierrez-Agüera, Sandra Rodriguez-Perales, Heleia Roca-Ho
Altres ajuts: European Food and Safety Authority, EFSA.PRAS.2018.04-CT1; Consejo Nacional de Ciencia y Tecnología, CB-2012-01-183467; Centro de Investigación Biomédica en Red en Cáncer, PID2019-104695RBI00; Asociación Española Contra el Cáncer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88b24beedf8b9074abdbcc4fcbcfa994
https://ddd.uab.cat/record/270581
https://ddd.uab.cat/record/270581
Autor:
Vianney Cortés-González, Patricia Pérez-Vera, Luis Quintana-Fernández, Daniel Martinez-Anaya, David Apam-Garduño, Cristina Villanueva-Mendoza
Publikováno v:
Ophthalmic Genetics. 40:584-587
Microphthalmia/anophthalmia (M/A) is considered a severe congenital malformation and is the cause of sight impairment worldwide, affecting 3%–12% of children. M/A, as a spectrum, can occur unilater...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d58084869c42738d4f87697f81a034f
https://doi.org/10.1080/13816810.2019.1698618
https://doi.org/10.1080/13816810.2019.1698618
Autor:
Roberto Cruz-Alcívar, P. Navarrete-Meneses, A. Reyes-León, A. González-Del Angel, V. Ulloa-Avilés, Patricia Pérez-Vera, A. I. Pedraza-Meléndez, A. González-Orsuna, S. Gómez-Carmona, Consuelo Salas-Labadía, David E. Cervantes-Barragán, Emiy Yokoyama-Rebollar, Esther Lieberman-Hernández, Adriana Ruiz-Herrera, Carola Durán-McKinster, D. Martínez-Anaya, V. Del Castillo-Ruiz, D. Suárez-Pérez, C. Villarroel-Cortés
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Pigmentary mosaicism constitutes a heterogeneous group of skin pigmentation alterations associated with multisystem involvement. The aim of this study was to establish a complete cytogenetic and molecular characterization of PM patients, e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ad97d1e0b6016f81af280efa02d09cc
http://link.springer.com/article/10.1186/s13023-019-1208-0
http://link.springer.com/article/10.1186/s13023-019-1208-0