Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Benjamín Gómez-Díaz"'
Autor:
Luz Berenice López-Hernández, Guillermina Avila-Ramírez, Ariadna Del Villar-Morales, Mónica Alejandra Anaya-Segura, Luis Angel Montes-Almanza, Froylan Arturo García-Martínez, Antonio Miranda-Duarte, Carlos Antonio Sosa-Flores, Martha Eunice Rodríguez-Arellano, Ileana Chavez-Maisterra, Alexandra Berenice Luna-Angulo, Miriam Pavelth Casillas-Ávila, Benjamín Gómez-Díaz
Publikováno v:
Muscles, Vol 2, Iss 4, Pp 389-399 (2023)
Several reports have provided evidence that there are genetic variants of genes such as MSTN, BDRKB2, ACTN3 and ADRB2 that are involved in a better response to adaptation during resistance or strength training, while other genes such as GRB14, AGT an
Externí odkaz:
https://doaj.org/article/aa8006c1b8294f28a22b2e6e6a0ec5e6
Autor:
Alexandra Luna-Angulo, Carlos Landa-Solís, Rosa Elena Escobar-Cedillo, Francisco Javier Estrada-Mena, Laura Sánchez-Chapul, Benjamín Gómez-Díaz, Paul Carrillo-Mora, Hamlet Avilés-Arnaut, Livier Jiménez-Hernández, Dulce Adeí Jiménez-Hernández, Antonio Miranda-Duarte
Publikováno v:
Medicina, Vol 60, Iss 7, p 1060 (2024)
Muscular dystrophies (MDs) are a heterogeneous group of diseases of genetic origin characterized by progressive skeletal muscle degeneration and weakness. There are several types of MDs, varying in terms of age of onset, severity, and pattern of the
Externí odkaz:
https://doaj.org/article/e79b2ab7db1b478f86638459f9ef60f1
Autor:
Edgar Oswaldo Zamora-González, Angel Herráez, Paula Daniela Gutiérrez-Muñoz, Olivia Torres-Bugarín, María Valentina Toral-Murillo, Benjamín Gómez-Díaz, Cecilia Adriana Calderón-Reyes, Norma Alejandra Vázquez-Cárdenas, Antonio Marín-Cruz, Marcela María José Rodríguez-Baeza, Nathaniel Lara-Palazuelos, Luz Berenice López-Hernández
Publikováno v:
Education Sciences, Vol 14, Iss 2, p 157 (2024)
The rapid evolution of biotechnology across various sectors, including agriculture, industry, and medicine, has profoundly transformed our comprehension of the world. Virtual laboratories (VLs) provide an immersive learning experience that can enhanc
Externí odkaz:
https://doaj.org/article/6d5f4ae371b149c78432b2d733c21b90
Autor:
Benjamín Gómez-Díaz, Edgar Oswaldo Zamora-González, Antonio Miranda-Duarte, Bladimir Roque-Ramírez, Norma Alejandra Vázquez-Cárdenas, Georgina Martínez-Gómez, Jhoana Martín del Campo, Erick Castillo-Jáuregui, Ángel Rafael Castro-Navarro, Antonio Marín-Cruz, Stephanie Rosas-Maldonado, Paulina Elizabeth Valdez-Anguiano, Reyna Araceli Barrera-López, Luz Berenice López-Hernández
Publikováno v:
Rare, Vol 1, Iss , Pp 100005- (2023)
Rare diseases (RDs) are serious and often fatal uncommon conditions with a high subjacent genetic origin. Since RD are not prevalent, knowledge regarding these diseases among health care providers and health students is scarce. The management of RD i
Externí odkaz:
https://doaj.org/article/15875f5852b04f129bf032647c2cb940
Autor:
Rosa Elena Escobar-Cedillo, Luz López-Hernández, Antonio Miranda-Duarte, María Dolores Curiel-Leal, Andrea Suarez-Ocón, Laura Sánchez-Chapul, Alexandra Berenice Luna-Angulo, Guillermina Ávila-Ramírez, Julia Angélica López-Hernández, Benjamín Gómez-Díaz
Publikováno v:
Folia Neuropathologica, Vol 59, Iss 3, Pp 276-283 (2021)
Muscular dystrophies are a group of well-defined genetic disorders characterized by the variable distribution of muscle wasting and progressive weakness. The diagnosis and treatment of these diseases remain challenging due to genetic heterogeneity an
Externí odkaz:
https://doaj.org/article/603df209725b4742932efdc90362ee5b
Autor:
Francisco Alejandro Ortiz-Sánchez, Aniel Jessica Leticia Brambila-Tapia, Luis Shigeo Cárdenas-Fujita, Christian Gabriel Toledo-Lozano, María Alejandra Samudio-Cruz, Benjamín Gómez-Díaz, Silvia García, Martha Eunice Rodríguez-Arellano, Edgar Oswaldo Zamora-González, Luz Berenice López-Hernández
Publikováno v:
Behavioral Sciences, Vol 13, Iss 2, p 120 (2023)
Suicide is considered a public health problem that affects families worldwide. Family functioning is the capability of the family system to fulfill needs during the stages of its development. In this study, we focused on evaluating family cohesion an
Externí odkaz:
https://doaj.org/article/2c4a23ddffb84042bf85729c337a6ef4
Autor:
Luz Berenice López-Hernández, Benjamín Gómez-Díaz, Alexandra Berenice Luna-Angulo, Mónica Anaya-Segura, David John Bunyan, Carolina Zúñiga-Guzman, Rosa Elena Escobar-Cedillo, Bladimir Roque-Ramírez, Luis Angel Ruano-Calderón, Héctor Rangel-Villalobos, Julia Angélica López-Hernández, Francisco Javier Estrada-Mena, Silvia García, Ramón Mauricio Coral-Vázquez
Publikováno v:
International Journal of Molecular Sciences, Vol 16, Iss 3, Pp 5334-5346 (2015)
Novel therapeutic approaches are emerging to restore dystrophin function in Duchenne Muscular Dystrophy (DMD), a severe neuromuscular disease characterized by progressive muscle wasting and weakness. Some of the molecular therapies, such as exon skip
Externí odkaz:
https://doaj.org/article/f7b9b3b5ce884427a1acd682237790b6
Autor:
Mónica Alejandra Anaya-Segura, Héctor Rangel-Villalobos, Gabriela Martínez-Cortés, Benjamín Gómez-Díaz, Ramón Mauricio Coral-Vázquez, Edgar Oswaldo Zamora-González, Silvia García, Luz Berenice López-Hernández
Publikováno v:
International Journal of Molecular Sciences, Vol 17, Iss 8, p 1334 (2016)
Duchenne Muscular Dystrophy (DMD) is an X-linked neuromuscular disorder in which the detection of female carriers is of the utmost importance for genetic counseling. Haplotyping with polymorphic markers and quantitation of creatine kinase levels (CK)
Externí odkaz:
https://doaj.org/article/59f0846258b24a5fb36224a187029f9c
Autor:
Guillermo Ceballos, Benjamín Gómez-Díaz, Israel Ramirez-Sanchez, Ana Lilia Cedeño-Garcidueñas, Modesto Lara-Hernandez, Aldo Moreno-Ulloa, Viridiana Navarrete-Yañez, Alejandra Garate-Carrillo, Judith Espinosa-Raya, Francisco Villarreal
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific reports, vol 11, iss 1
Scientific Reports
Scientific reports, vol 11, iss 1
Scientific Reports
We examined in a rat model of Gulf War illness (GWI), the potential of (−)-epicatechin (Epi) to reverse skeletal muscle (SkM) atrophy and dysfunction, decrease mediators of inflammation and normalize metabolic perturbations. Male Wistar rats (n = 1
Autor:
Laura Sánchez-Chapul, Rosa Elena Escobar-Cedillo, Luz Berenice López-Hernández, Andrea Suarez-Ocón, Alexandra Luna-Angulo, María Dolores Curiel-Leal, Julia Angélica López-Hernández, Antonio Miranda-Duarte, Guillermina Avila-Ramirez, Benjamín Gómez-Díaz
Publikováno v:
Folia Neuropathologica, Vol 59, Iss 3, Pp 276-283 (2021)
Muscular dystrophies are a group of well-defined genetic disorders characterized by the variable distribution of muscle wasting and progressive weakness. The diagnosis and treatment of these diseases remain challenging due to genetic heterogeneity an