Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Adriana Ochoa"'
Autor:
Adriana Ochoa-Sanchez, Padmavati Sahare, Surajit Pathak, Antara Banerjee, Miriam Estevez, Asim K. Duttaroy, Gabriel Luna-Bárcenas, Sujay Paul
Publikováno v:
Frontiers in Pharmacology, Vol 15 (2024)
Colorectal cancer (CRC) remains a significant global health concern, being the third most diagnosed cancer in men and the second most diagnosed cancer in women, with alarming mortality rates. Natural phytochemicals have gained prominence among variou
Externí odkaz:
https://doaj.org/article/4fb9a53d58f1464b842979b0fc8e5209
Autor:
Adriana Ochoa-Sanchez, Gabriela Perez-Sanchez, A. Marianna Torres-Ledesma, Juan Pablo R. Valdez, Gabriel Rinaldi, B?rbara B. Moguel, Christian Molina-Aguilar
Publikováno v:
Re:GEN Open, Vol 1, Iss 1, Pp 75-82 (2021)
Background: Genome editing mediated by clustered regularly interspaced short palindromic repeat -CRISPR-Cas- was first reported using cell lines in 2012, and since then, its applications in other systems have steadily increased. However, this approac
Externí odkaz:
https://doaj.org/article/41838f7dbdb84441994172a70cd957af
Autor:
Rodrigo Barquera, Joaquin Zuniga, José Flores-Rivera, Teresa Corona, Bridget S. Penman, Diana Iraíz Hernández-Zaragoza, Manuel Soler, Letisia Jonapá-Gómez, Kalyan C. Mallempati, Petra Yescas, Adriana Ochoa-Morales, Konstantinos Barsakis, José Artemio Aguilar-Vázquez, Maricela García-Lechuga, Michael Mindrinos, María Yunis, Luis Jiménez-Alvarez, Lourdes Mena-Hernández, Esteban Ortega, Alfredo Cruz-Lagunas, Víctor Hugo Tovar-Méndez, Julio Granados, Marcelo Fernández-Viña, Edmond Yunis
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-22 (2020)
Abstract Here we studied HLA blocks and haplotypes in a group of 218 Lacandon Maya Native American using a high-resolution next generation sequencing (NGS) method. We assessed the genetic diversity of HLA class I and class II in this population, and
Externí odkaz:
https://doaj.org/article/82c8f093dc154ddc8cdaf23e543b5c4c
Autor:
Iris E. Martínez-Juárez, Aurelio Jara-Prado, Adriana Ochoa-Morales, Nancy Castro-Veloz, Andrea Santos-Peyret, Jimena Armenta-Báez, Mario A. Sebastián-Díaz
Publikováno v:
Gaceta Médica de México, Vol 157, Iss 4 (2021)
Externí odkaz:
https://doaj.org/article/deb3e2020d0f4af08a2139dcce0b8518
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e83365 (2013)
Droughts are among the most important disturbance events for stream ecosystems; they not only affect stream hydrology but also the stream biota. Although desiccation of streams is common in Mediterranean regions, phases of dryness in headwaters have
Externí odkaz:
https://doaj.org/article/14f4088409be48559e5a8e4a06ebe628
Publikováno v:
Multiple Sclerosis International, Vol 2012 (2012)
Multiple Sclerosis (MS) is a highly polymorphic disease characterized by different neurologic signs and symptoms. In MS, racial and genetic factors may play an important role in the geographic distribution of this disease. Studies have reported the p
Externí odkaz:
https://doaj.org/article/70a3df28fb634c16bc58bfde64d084b3
Autor:
Leo Bayliss, Víctor Galvez, Adriana Ochoa-Morales, Mireya Chávez-Oliveros, Yaneth Rodríguez-Agudelo, Guillermo Delgado-García, Marie Catherine Boll
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 77, Iss 8, Pp 574-578
ABSTRACT Huntington disease (HD) is an autosomal dominant genetic disorder characterized by movement disorders, cognitive impairment, and psychiatric symptoms. Relatives of HD patients experience a great burden as the latter suffer from altered socia
Externí odkaz:
https://doaj.org/article/a87ca398014745a1bb76c2b4446fd145
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
Autor:
Timothy Lee, Avi Landman, Carlos Garcia Ocasio, Elmira Veselinovic, Adriana Ochoa, Mustafa Mohamed, Muhammad-Atif Zubairi
Publikováno v:
Wednesday, April 26.
Autor:
Miguel Ángel Ramírez-García, David José Dávila-Ortiz de Montellano, Leticia Martínez-Ruano, Adriana Ochoa-Morales, Sandra Romero-Hidalgo, Juan Carlos Zenteno, Petra Yescas-Gómez
Publikováno v:
Neurodegenerative Diseases. 22:34-42
Introduction: There are reports of different clinical statuses in carriers of intermediate alleles (IAs) of CAG trinucleotide repeats in the HTT gene, from individuals affected by a clinical picture indistinguishable from Huntington’s disease (HD)