Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Adriana Ochoa‐Morales"'
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
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
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:
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)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::115085237c3effc122d2ffa3f408018b
https://doi.org/10.1159/000526260
https://doi.org/10.1159/000526260
Autor:
Gustavo Padron-Rivera, Angel Omar Romero-Molina, Rosalinda Diaz, Israel Vaca-Palomares, Adriana Ochoa-Morales, César Romero-Rebollar, Amanda Chirino-Pérez, Juan Fernandez-Ruiz
Publikováno v:
Neurodegenerative Diseases. 22:24-28
Background: Recent resting-state functional magnetic resonance imaging studies have reported abnormal functional connectivity (FC) in the prefrontal cortex (PFC)-striatum circuit in patients with premanifest Huntington’s disease (HD). However, ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6732cf0910f79e865bc99bf7ff54957
https://doi.org/10.1159/000526778
https://doi.org/10.1159/000526778
Autor:
Adriana Ochoa-Morales, Ana Fresan-Orellana, Miguel Ángel Ramírez-García, Horacio Márquez-González, Iris E. Martínez-Juárez, Mayra López-Uribe, Carol Zuniga-García, Aurelio Jara-Prado, Jorge Luis Guerrero-Camacho, David José Dávila-Ortiz de Montellano
Publikováno v:
Epilepsy & Behavior. 144:109268
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7632f0806a33dac9f02fd824708ea5e0
https://doi.org/10.1016/j.yebeh.2023.109268
https://doi.org/10.1016/j.yebeh.2023.109268
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:
Maricela García-Lechuga, Manuel Soler, Diana Iraíz Hernández-Zaragoza, Marcelo Fernandez-Vina, Michael N. Mindrinos, Víctor Hugo Tovar-Méndez, Bridget S. Penman, Kalyan C. Mallempati, Lourdes Mena-Hernández, Alfredo Cruz-Lagunas, Teresa Corona, Joaquín Zúñiga, Petra Yescas, María Yunis, Konstantinos Barsakis, José Flores-Rivera, Esteban Ortega, Luis Jiménez-Alvarez, Julio Granados, Adriana Ochoa-Morales, José Artemio Aguilar-Vázquez, Edmond J. Yunis, Rodrigo Barquera, Letisia Jonapá-Gómez
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-22 (2020)
Scientific Reports
Scientific Reports
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 determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::744ce955d1062552e927b551bbddecb0
http://link.springer.com/article/10.1038/s41598-020-58897-5
http://link.springer.com/article/10.1038/s41598-020-58897-5
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 medica de Mexico. 157(4)
A prevalence of 1 to 71% of electroencephalogram (EEG) abnormalities has been reported in asymptomatic relatives of patients with juvenile myoclonic epilepsy (JME).To determine the frequency of EEG abnormalities in asymptomatic relatives of patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e57711e1622e90072089b1a8d2dd576a
https://pubmed.ncbi.nlm.nih.gov/35133334
https://pubmed.ncbi.nlm.nih.gov/35133334