Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Celia Nohemí Sánchez-Domínguez"'
Autor:
David Emmanuel Kubelis-López, Natalia Aranza Zapata-Salazar, Mauricio Andrés Salinas-Santander, Celia Nohemí Sánchez-Domínguez, Jesús Antonio Morlett-Chávez, Jorge Ocampo-Candiani
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 98, Iss 3, Pp 376-378 (2023)
Externí odkaz:
https://doaj.org/article/3de62a6ba20c45e4b293fa175ee4b22c
Autor:
Juan Angel Garcia-Quiñones, Celia Nohemí Sánchez-Domínguez, María Fernanda Serna-Rodríguez, Iván Alberto Marino-Martínez, Ana María Rivas-Estilla, Antonio Alí Pérez-Maya
Publikováno v:
Archives of Suicide Research. :1-19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c744aa523a68addaaf115ec27d2356e7
https://doi.org/10.1080/13811118.2023.2176269
https://doi.org/10.1080/13811118.2023.2176269
Autor:
Jorge Ocampo-Candiani, Natalia Aranza Zapata Salazar, David Emmanuel Kubelis-López, Mauricio Andrés Salinas-Santander, Celia Nohemí Sánchez-Domínguez, Ana Cecilia Xolalpa-Rosales, Marely Eugenia Gómez-Galindo
Vitiligo is the most common depigmenting disease characterized by achromic macules due to selective loss of melanocytes. The pathogenesis remains poorly elucidated, and multiple hypotheses exists regarding its pathogenesis. Evidence suggests that str
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45c747169a74e88ddbd52c35f8e60210
https://doi.org/10.21203/rs.3.rs-1498881/v1
https://doi.org/10.21203/rs.3.rs-1498881/v1
Autor:
Víctor Manuel Peña Martínez, Alberto Camacho‑Morales, Rocky S. Tuan, Vanessa Pérez‑Silos, Celia Nohemí Sánchez‑Domínguez, Alejandro Garcia‑Ruiz, Jorge Lara Arias, Rosalio Ramos Payan, Hang Lin, Viktor J. Romero Díaz, Iván Alberto Marino Martínez, Lizeth Fuentes Mera, Yanko Castro Govea, Ana María Rivas Estilla, Nidia K. Moncada‑Saucedo
Publikováno v:
Experimental and Therapeutic Medicine
Joint cartilage damage affects 10-12% of the world's population. Medical treatments improve the short-term quality of life of affected individuals but lack a long-term effect due to injury progression into fibrocartilage. The use of mesenchymal stem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0be0b836f5593ee55d3dec90d0f0e1b3
https://doi.org/10.3892/etm.2021.10717
https://doi.org/10.3892/etm.2021.10717
Autor:
David Emmanuel Kubelis‑Lopez, Uwe Wollina, Torello Lotti, Osvaldo Tomás Vázquez Martínez, Salvador Luis Said‑Fernandez, Jorge Ocampo Candiani, Celia Nohemí Sánchez‑Domínguez, Mauricio Andres Salinas‑Santander, Natalia Aranza Zapata‑Salazar, Herminia Guadalupe Martínez Rodríguez
Publikováno v:
Experimental and Therapeutic Medicine
Vitiligo is a skin disorder characterized by depigmentation of the skin due to a lack of melanin. This condition affects men and woman of all ages and its incidence is not restricted by ethnicity or region. Vitiligo is a multifactorial disease, in wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62b55b7e3b87936d39fb65d1e35cc7f3
https://pubmed.ncbi.nlm.nih.gov/33717255
https://pubmed.ncbi.nlm.nih.gov/33717255
Autor:
Celia Nohemí Sánchez‑Domínguez, Melissa Náñez‑Marín, Diana Aráiz‑Hernández, Raquel Garza Guajardo, Jesus Rolando Delgado‑Balderas, Brenda Soto‑García, Ana María Rivas Estilla, Guillermo Vízcarra‑Mata, Hugo Leonid Gallardo‑Blanco, Marco Alberto Ocaña‑Munguía, Juan Felipe Yee‑De León, David Hernández Barajas, Aldo Missael García Bailón, Lauro Salvador Gómez Guerra
Publikováno v:
Oncology Letters
The presence of the genetic variants of the steroid 5-alpha reductase 2 enzyme, which is encoded by the SRD5A2 gene, has been associated with an increased risk of developing prostate cancer among certain ethnic groups. However, these molecular studie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e02becdb57e45c36ca5aa2f11bbd84c
https://pubmed.ncbi.nlm.nih.gov/32989395
https://pubmed.ncbi.nlm.nih.gov/32989395
Autor:
Ricardo Martín Cerda Flores, Celia Nohemí Sánchez‑Domínguez, Jesús Zacarías Villarreal Pérez, Laura Elia Martinez‑Garza, Juana Mercedes Gutiérrez Valverde, Hugo Leonid Gallardo‑Blanco, Iris Carmen Torres‑Muñoz, Esther Carlota Gallegos Cabriales, Andrés Jiménez Figueroa, Fernando J. Lavalle Gonzalez
Publikováno v:
Experimental and Therapeutic Medicine. 13:523-529
The aim of the present study was to investigate whether genetic markers considered risk factors for metabolic syndromes, including dyslipidemia, obesity and type 2 diabetes mellitus (T2DM), can be applied to a Northeastern Mexican population. A total
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fcaa4d4a5a4b0d4aac9018788455f01b
https://doi.org/10.3892/etm.2016.3990
https://doi.org/10.3892/etm.2016.3990
Autor:
Rocio Ortiz‑Lopez, Hugo Leonid Gallardo‑Blanco, Celia Nohemí Sánchez‑Domínguez, Mauricio Andres Salinas‑Santander
Publikováno v:
Experimental and Therapeutic Medicine.
Biotransformation is an enzyme-catalyzed process in which the body converts endogenous compounds, xenobiotics and toxic substances into harmless or easily excreted metabolites. The biotransformation reactions are classified as phase I and II reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c58a227948caa129f4523865bfb5679a
https://doi.org/10.3892/etm.2018.6184
https://doi.org/10.3892/etm.2018.6184
Autor:
María Antonia González-Zavala, Celia Nohemí Sánchez‑Domínguez, Hugo Leonid Gallardo‑Blanco, Miguel Ángel González-Madrazo, Sandra Cecilia Esparza González, Ana Cecilia Cepeda Nieto, Mauricio Andres Salinas‑Santander, Rafael Baltazar Reyes León‑Cachón
Publikováno v:
Biomedical Reports. 4:107-111
Obesity is currently considered an inflammatory condition associated with autoimmune diseases, suggesting a common origin. Among other factors, candidate genes may explain the development of this disease. Polymorphisms in the tumor necrosis factor α
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9074cb6ac07451a60583ba8d1c473ed6
https://doi.org/10.3892/br.2015.534
https://doi.org/10.3892/br.2015.534
Autor:
Mauricio Andrés Salinas-Santander, Cristina Susana Cantu-Salinas, Jorge Ocampo-Candiani, Victor de Jesus Suarez-Valencia, Jennifer Guadalupe Ramirez-Guerrero, Celia Nohemi Sanchez-Dominguez
Publikováno v:
Anais Brasileiros de Dermatologia, Vol 95, Iss 3, Pp 283-288 (2020)
Abstract Background: Alopecia areata is an autoimmune disease that produces non-scarring hair loss around the body. Gene variants of the cytotoxic T-lymphocyte antigen 4 (CTLA4) gene, a negative regulator of T-cell response, have been associated with
Externí odkaz:
https://doaj.org/article/195230ede8a44b9eafb5c8bb5928a747