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Cerebellum (London, England)
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October 8, 2013
Recessive spinocerebellar ataxia with paroxysmal cough attacks: a report of five cases
Luis Velázquez-Pérez, Rigoberto González-Piña, Roberto Rodríguez-Labrada, et al.
Aging Cell
|
January 28, 2025
Targeting CRM1 for Progeria Syndrome Therapy
Adriana Soto-Ponce, Marlon De Ita, Susana Castro-Obregón, et al.
Biomolecules
|
February 3, 2021
Transcriptome Analysis Reveals Altered Inflammatory Pathway in an Inducible Glial Cell Model of Myotonic Dystrophy Type 1
Cuauhtli N Azotla-Vilchis, Daniel Sanchez-Celis, Luis E Agonizantes-Juárez, et al.
Genes
|
September 23, 2022
Clustering of Genetic Anomalies of Cilia Outer Dynein Arm and Central Apparatus in Patients with Transposition of the Great Arteries
Marlon De Ita, Javier Gaytán-Cervantes, Bulmaro Cisneros, et al.
Aging Cell
|
July 16, 2019
Enhanced nuclear protein export in premature aging and rescue of the progeria phenotype by modulation of CRM1 activity
Ian García-Aguirre, Alma Alamillo-Iniesta, Ruth Rodríguez-Pérez, et al.
International Journal of Molecular Sciences
|
October 16, 2024
Current Overview of Spinocerebellar Ataxia Type 7 in Mexican Population: Challenges in Specialized Care for a Rare Disease
César M Cerecedo-Zapata, Yessica S Tapia-Guerrero, José A Ramírez-González, et al.
Cerebellum (London, England)
|
February 23, 2020
Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean
Roberto Rodríguez-Labrada, Ana Carolina Martins, Jonathan J Magaña, et al.
Cell & Bioscience
|
March 25, 2026
The molecular mechanism underlying the differential subcellular distribution of dystrophin Dp71 isoforms
Alma Alamillo-Iniesta, Griselda Velez-Aguilera, Feliciano Monterrubio-Ledezma, et al.
Genes
|
December 30, 2025
Fifteen Years of Myotonic Dystrophy Type 1 in Mexico: Clinical, Molecular, and Socioeconomic Insights from a National Reference Cohort
César M Cerecedo-Zapata, Araceli Guerra-Grajeda, Luz C Márquez-Quiróz, et al.
Cerebellum (London, England)
|
June 8, 2014
Comprehensive study of early features in spinocerebellar ataxia 2: delineating the prodromal stage of the disease
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Edilia M Cruz-Rivas, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 104) with videos related to
Sort By:
Page
of 11
Cerebellum (London, England)
|
October 8, 2013
Recessive spinocerebellar ataxia with paroxysmal cough attacks: a report of five cases
Luis Velázquez-Pérez, Rigoberto González-Piña, Roberto Rodríguez-Labrada, et al.
Aging Cell
|
January 28, 2025
Targeting CRM1 for Progeria Syndrome Therapy
Adriana Soto-Ponce, Marlon De Ita, Susana Castro-Obregón, et al.
Biomolecules
|
February 3, 2021
Transcriptome Analysis Reveals Altered Inflammatory Pathway in an Inducible Glial Cell Model of Myotonic Dystrophy Type 1
Cuauhtli N Azotla-Vilchis, Daniel Sanchez-Celis, Luis E Agonizantes-Juárez, et al.
Genes
|
September 23, 2022
Clustering of Genetic Anomalies of Cilia Outer Dynein Arm and Central Apparatus in Patients with Transposition of the Great Arteries
Marlon De Ita, Javier Gaytán-Cervantes, Bulmaro Cisneros, et al.
Aging Cell
|
July 16, 2019
Enhanced nuclear protein export in premature aging and rescue of the progeria phenotype by modulation of CRM1 activity
Ian García-Aguirre, Alma Alamillo-Iniesta, Ruth Rodríguez-Pérez, et al.
International Journal of Molecular Sciences
|
October 16, 2024
Current Overview of Spinocerebellar Ataxia Type 7 in Mexican Population: Challenges in Specialized Care for a Rare Disease
César M Cerecedo-Zapata, Yessica S Tapia-Guerrero, José A Ramírez-González, et al.
Cerebellum (London, England)
|
February 23, 2020
Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean
Roberto Rodríguez-Labrada, Ana Carolina Martins, Jonathan J Magaña, et al.
Cell & Bioscience
|
March 25, 2026
The molecular mechanism underlying the differential subcellular distribution of dystrophin Dp71 isoforms
Alma Alamillo-Iniesta, Griselda Velez-Aguilera, Feliciano Monterrubio-Ledezma, et al.
Genes
|
December 30, 2025
Fifteen Years of Myotonic Dystrophy Type 1 in Mexico: Clinical, Molecular, and Socioeconomic Insights from a National Reference Cohort
César M Cerecedo-Zapata, Araceli Guerra-Grajeda, Luz C Márquez-Quiróz, et al.
Cerebellum (London, England)
|
June 8, 2014
Comprehensive study of early features in spinocerebellar ataxia 2: delineating the prodromal stage of the disease
Luis Velázquez-Pérez, Roberto Rodríguez-Labrada, Edilia M Cruz-Rivas, et al.
Page
of 11