Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Margarita Valdes-Flores"'
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:
José Guillermo Buendía-Pazarán, Edgar Hernández-Zamora, Armando O. Rodríguez-Olivas, Leonora Casas-Ávila, Margarita Valdés-Flores, Elba Reyes-Maldonado
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-6 (2022)
Abstract Background Legg–Calvé–Perthes disease (LCPD) is the avascular osteonecrosis of the proximal femoral epiphysis. It is a rare disease of unclear etiology in children, although alterations in coagulation or the collagen gene have been desc
Externí odkaz:
https://doaj.org/article/2cf66fbe04374e1c93d1bec63c0e6892
Autor:
Susana Kofman-Alfaro, Guadalupe Maya-Núñez, Sergio A. Cuevas-Covarrubias, Ana Luisa Jiménez-Vaca, Margarita Valdes-Flores, M.R. Rivera-Vega, Luz María González-Huerta
Publikováno v:
Journal of Investigative Dermatology. 119:972-975
Steroid sulfatase deficiency results in X-linked ichthyosis, an inborn error of metabolism in which the principal molecular defect is the complete deletion of the steroid sulfatase gene and flanking markers. Mosaicism for the steroid sulfatase gene h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117c6634ed55dc247d9a332d00e758c1
https://doi.org/10.1046/j.1523-1747.2002.t01-1-00185.x
https://doi.org/10.1046/j.1523-1747.2002.t01-1-00185.x
Autor:
Eréndira Estrada‐Villaseñor, Margarita Valdés‐Flores, Abelardo Meneses‐García, Phaedra Silva‐Bermudez, Raul Pichardo‐Bahena, Pedro Ostoa‐Saloma, Gabriela Mercado‐Celis, Ernesto D. Delgado‐Cedillo, Anell Olivos‐Meza, Carlos Landa‐Solís
Publikováno v:
Engineering in Life Sciences, Vol 21, Iss 8-9, Pp 539-543 (2021)
Abstract Two‐dimensional (2D) culture of cells from giant cell tumor of bone (GCTB) is affected by loss of the multinucleated giant cells in subsequent passages. Therefore, there is limited time to study GCTB with all its histological components in
Externí odkaz:
https://doaj.org/article/754585d0085a453d8884959a6a36b098
Autor:
Margarita Valdes Flores
Publikováno v:
Topics in Osteoporosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a762d158767d2bf4267c78763300ab22
https://doi.org/10.5772/50259
https://doi.org/10.5772/50259
Autor:
Adriana Solis-Vivanco, Mónica Santamaría-Olmedo, Dalila Rodríguez-Juárez, Margarita Valdés-Flores, Carlos González-Castor, Rafael Velázquez-Cruz, Eric Ramírez-Salazar, Ana Cristina García-Ulloa, Alberto Hidalgo-Bravo
Publikováno v:
Diagnostics, Vol 12, Iss 10, p 2275 (2022)
Diabetic retinopathies are important disabling conditions. Micro-RNAs (miRNAs) are regulators of gene expression and diseases can change their expression. Our aim was to analyze the expression of miRNAs in serum and vitreous samples from patients wit
Externí odkaz:
https://doaj.org/article/7027d9a5d9224fa3b1a9c34f4622400e
Autor:
Margarita Valdés-Flores, Leonora Casas-Avila, Edgar Hernández-Zamora, Susana Kofman, Alberto Hidalgo-Bravo
Publikováno v:
Jornal de Pediatria, Vol 92, Iss 1, Pp 58-64 (2016)
ABSTRACT OBJECTIVE: Arthrogryposis multiplex congenita is a relatively rare neuromuscular syndrome, with a prevalence of 1:3000-5000 newborns. In this study, the authors describe the clinical features of a group of 50 unrelated Mexican patients with
Externí odkaz:
https://doaj.org/article/1aca071c95ff48b993679dc3a694fc2f