Zobrazeno 1 - 10
of 16
pro vyhledávání: '"María del Pilar Navarrete Meneses"'
Autor:
Dafné Moreno Lorenzana, María del Rocío Juárez Velázquez, Adriana Reyes León, Daniel Martínez Anaya, Adrián Hernández Monterde, Consuelo Salas Labadía, María del Pilar Navarrete Meneses, Marta Zapata Tarrés, Luis Juárez Villegas, Berenice Jarquín Ramírez, Rocío Cárdenas Cardós, Martha Herrera Almanza, Rogelio Paredes Aguilera, Patricia Pérez Vera
Publikováno v:
The Journal of Pathology: Clinical Research, Vol 7, Iss 4, Pp 410-421 (2021)
Abstract 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 ove
Externí odkaz:
https://doaj.org/article/3c435bf0b67c413196f05647867b2feb
Autor:
María del Pilar Navarrete-Meneses, Consuelo Salas-Labadía, Fernando Gómez-Chávez, Patricia Pérez-Vera
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 6, p 3284 (2024)
The long-term effects of environmental pollution have been of concern as several pollutants are carcinogenic, potentially inducing a variety of cancers, including childhood cancer, which is a leading cause of death around the world and, thus, is a pu
Externí odkaz:
https://doaj.org/article/4866cebed57b4b48aeb25a5597c747b7
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:
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
Publikováno v:
Reviews on Environmental Health. 34:197-210
Pyrethroid insecticides are commonly used worldwide. The chronic effects of these compounds are of concern given that epidemiological studies have suggested an association with hematological cancer, particularly in children. However, the biological e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac09344f6ceaefaab2011b8410e545a5
https://doi.org/10.1515/reveh-2018-0070
https://doi.org/10.1515/reveh-2018-0070
Autor:
C. Salas-Labadía, A. I. Pedraza-Meléndez, P. Pérez-Vera, María del Pilar Navarrete-Meneses, D. Moreno-Lorenzana
Publikováno v:
Journal of Applied Toxicology. 38:1262-1270
Pesticides are commonly used worldwide and almost every human is potentially exposed to these chemicals. Exposure to pesticides such as permethrin and malathion has been associated with hematological malignancies in epidemiological studies. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f5247a3619c2f108857cabf4e052ab2
https://doi.org/10.1002/jat.3638
https://doi.org/10.1002/jat.3638
Publikováno v:
Boletín Médico Del Hospital Infantil de México (English Edition). 74:243-264
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer. It is well-known that genetic alterations constitute the basis for the etiology of ALL. However, genetic abnormalities are not enough for the complete development of the disease,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::431c3b576b53fe64a5906fc9bfea6b1e
https://doi.org/10.1016/j.bmhime.2018.01.004
https://doi.org/10.1016/j.bmhime.2018.01.004
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 74, Iss 4, Pp 243-264 (2017)
Resumen La leucemia linfoblastica aguda (LLA) es el tipo de cancer mas frecuente en ninos. Aunque se sabe que las alteraciones geneticas constituyen la base de la etiologia de la LLA, se ha demostrado que no son suficientes para el desarrollo leucemi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a95816f52aeca6dcddca281e945bbab
https://doi.org/10.1016/j.bmhimx.2017.02.005
https://doi.org/10.1016/j.bmhimx.2017.02.005