Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Rosalba Sevilla‐Montoya"'
Autor:
Eibar E. Cabrera-Aldana, Yalbi I. Balderas-Martinez, Rafael Velázquez-Cruz, Luis B. Tovar-y-Romo, Rosalba Sevilla-Montoya, Angelina Martínez-Cruz, Claudia Martinez-Cordero, Margarita Valdes-Flores, Monica Santamaria-Olmedo, Alberto Hidalgo-Bravo, Gabriel Guízar-Sahagún
Publikováno v:
Current Issues in Molecular Biology, Vol 45, Iss 9, Pp 7476-7491 (2023)
Traumatic spinal cord injury (SCI) causes irreversible damage leading to incapacity. Molecular mechanisms underlying SCI damage are not fully understood, preventing the development of novel therapies. Tamoxifen (TMX) has emerged as a promising therap
Externí odkaz:
https://doaj.org/article/5e298bd4fd7744f3b6368f500ef3150c
Autor:
Judit A. Ramírez-Rosete, Alonso Hurtado-Vazquez, Antonio Miranda-Duarte, Sergio Peralta-Cruz, Ramiro Cuevas-Olivo, José Antonio Martínez-Junco, Rosalba Sevilla-Montoya, Berenice Rivera-Paredez, Rafael Velázquez-Cruz, Margarita Valdes-Flores, Claudia Rangel-Escareno, Gerardo J. Alanis-Funes, Laura Abad-Azpetia, Sacnicte G. Grimaldo-Galeana, Monica G. Santamaría-Olmedo, Alberto Hidalgo-Bravo
Publikováno v:
Diagnostics, Vol 14, Iss 9, p 898 (2024)
Diagnosis of developmental dysplasia of the hip (DDH) mostly relies on physical examination and ultrasound, and both methods are operator-dependent. Late detection can lead to complications in young adults. Current evidence supports the involvement o
Externí odkaz:
https://doaj.org/article/d91167f0c8c848e59b21e5c12274dcf7
Autor:
Diana G. Rogel-Ayala, José Esteban Muñoz-Medina, Valeria Dejanira Vicente-Juárez, Patricia Grether-González, Deneb Algedi Morales-Barquet, Alfonso de Jesús Martínez-García, María Olga Leticia Echaniz-Aviles, Rosalba Sevilla-Montoya, Alejandro Martínez-Juárez, Jazmin Artega-Vázquez, Javier Angeles-Martínez, Gilberto Vargas-Alarcón, Alberto Hidalgo-Bravo, Irma Eloisa Monroy-Muñoz
Publikováno v:
Diagnostics, Vol 13, Iss 15, p 2558 (2023)
Patent ductus arteriosus (PDA) is frequent in preterm newborns, and its incidence is inversely associated with the degree of prematurity. The first choice of pharmacological treatment is ibuprofen. Several genes, including EPAS1, have been proposed a
Externí odkaz:
https://doaj.org/article/76d9012f588240b5a2325abddd056457
Autor:
Rosalba Sevilla-Montoya, Maria de Jesus Zavaleta-Abreu, Gloria Queipo, Silvia Sanchez, Sara Frias, Alberto Hidalgo-Bravo, Patricia Grether-González
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 3, Pp 526-529 (2021)
Objective: Sex chromosome mosaicism remains challenging in the study of disorders of sex development (DSD). Aneuploid cells in the developing gonad play a major role in sex determination. Therefore, it is necessary acknowledge their presence by diffe
Externí odkaz:
https://doaj.org/article/7ab9f009ebb34de08dce2cfc1b968425
Autor:
Rosalba Sevilla-Montoya, Addy C. Helguera-Reppeto, Irma E. Monroy-Muñoz, Tania A. Vargas-Pavia, Elías I. Valdés-Montoya, Mario Solis-Paredes, Johnatan Torres-Torres, Rafael Velazquez-Cruz, José Esteban Muñoz-Medina, Claudia Martinez-Cordero, Alberto Hidalgo-Bravo
Publikováno v:
Diagnostics, Vol 13, Iss 7, p 1338 (2023)
COVID-19 forced us to investigate risk factors to provide the best medical attention, especially in vulnerable groups, such as pregnant patients. Studies in other populations have analyzed blood groups in relation to infection, complications, and dea
Externí odkaz:
https://doaj.org/article/2ab92514ebad466b9abae643c2d08e84
Autor:
José Romo-Yáñez, Rosalba Sevilla-Montoya, Edith Pérez-González, Josiff Flores-Reyes, Estibalitz Laresgoiti-Servitje, Salvador Espino-Sosa, Mauricio Domínguez-Castro, Guadalupe Razo-Aguilera, Alberto Hidalgo-Bravo, Mónica Aguinaga-Ríos
Publikováno v:
Cirugía y Cirujanos, Vol 90, Iss 2 (2022)
Aim: Analysis of male infertility by molecular methods has increased since recognition of genetic risk factors. The AZFa, AZFb, AZFc, and gr/gr regions on the Y-chromosome can cause male infertility. The aim of this study was to determine the prevale
Externí odkaz:
https://doaj.org/article/d6eb27842650450c853d6bf180ee9a2c
Autor:
Juan Mario Solis-Paredes, Araceli Montoya-Estrada, Adriana Cruz-Rico, Enrique Reyes-Muñoz, Javier Perez-Duran, Salvador Espino y Sosa, Victor Ranferi Garcia-Salgado, Rosalba Sevilla-Montoya, Raigam Jafet Martinez-Portilla, Guadalupe Estrada-Gutierrez, Juan Alexander Gomez-Ruiz, Paloma Mateu-Rogell, Jose Rafael Villafan-Bernal, Lourdes Rojas-Zepeda, Maria del Carmen Perez-Garcia, Johnatan Torres-Torres
Publikováno v:
Viruses, Vol 14, Iss 4, p 723 (2022)
Oxidative stress (OS) induced by SARS-CoV-2 infection may play an important role in COVID-19 complications. However, information on oxidative damage in pregnant women with COVID-19 is limited. Objective: We aimed to compare lipid and protein oxidativ
Externí odkaz:
https://doaj.org/article/7eb62941cfcd4df19837dfdcb4ef6392
Autor:
Adriana PerezGrovas‐Saltijeral, Adriana Ochoa‐Morales, Aurelio Jara‐Prado, Rafael Velázquez‐Cruz, Berenice Rivera‐Paredez, David Dávila‐OrtizdeMontellano, Edmar O. Benítez‐Alonso, Mónica Santamaría‐Olmedo, Rosalba Sevilla‐Montoya, Ernesto Marfil‐Marín, Margarita Valdés‐Flores, Leticia Martínez‐Ruano, Alejandra Camacho‐Molina, Alberto Hidalgo‐Bravo
Publikováno v:
European Journal of Neurology. 30:612-621
Juvenile-onset Huntington disease (JHD) is defined when symptoms initiate before 20 years of age. Mechanisms explaining differences between juvenile and adult onset are not fully understood. Our aim was to analyze the distribution of initial symptoms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2115593f24b57e360362b65d56e0a95
https://doi.org/10.1111/ene.15644
https://doi.org/10.1111/ene.15644
Autor:
Aurelio Jara-Prado, Rosalba Sevilla-Montoya, Alejandra Camacho-Molina, Ernesto Marfil-Marin, Adriana Ochoa-Morales, Margarita Valdés-Flores, Adriana PerezGrovas-Saltijeral, Mónica Santamaría-Olmedo, Alberto Hidalgo-Bravo
Publikováno v:
Molecular Neurobiology. 58:6222-6231
Huntington disease (HD) is the most common neurogenetic disorder caused by expansion of the CAG repeat in the HTT gene; nevertheless, the molecular bases of the disease are not fully understood. Non-coding RNAs have demonstrated to be involved in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90a7696439524c763e82940894ec8b20
https://doi.org/10.1007/s12035-021-02536-1
https://doi.org/10.1007/s12035-021-02536-1
Autor:
Alberto Hidalgo-Bravo, Rosalba Sevilla-Montoya, Maria de Jesus Zavaleta-Abreu, Sara Frías, Silvia Sánchez, Gloria Queipo, Patricia Grether-González
Publikováno v:
Taiwanese Journal of Obstetrics & Gynecology, Vol 60, Iss 3, Pp 526-529 (2021)
Objective Sex chromosome mosaicism remains challenging in the study of disorders of sex development (DSD). Aneuploid cells in the developing gonad play a major role in sex determination. Therefore, it is necessary acknowledge their presence by differ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2b1c105dfe008bc9207de52b7e5f640
https://doi.org/10.1016/j.tjog.2021.03.025
https://doi.org/10.1016/j.tjog.2021.03.025