Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Frøyl"'
Autor:
Andres Ordoñes‐Saucedo, Bruno Eduardo Reyes‐Torres, Karen Kortright‐Maldonado, Erika K. Tenorio‐Aguirre, Pedro Rodríguez‐Henríquez, Froylan D. Martínez‐Sánchez
Publikováno v:
Clinical Case Reports, Vol 12, Iss 11, Pp n/a-n/a (2024)
ABSTRACT Acute pancreatitis (AP) is a rare but life‐threatening complication in patients with systemic lupus erythematosus (SLE). The case highlights the diagnostic challenges and treatment complexities in managing SLE‐associated pancreatitis. A
Externí odkaz:
https://doaj.org/article/29f6de16b02a4ab3b6ae9dbf6c47daa0
Autor:
Froylan D. Martínez-Sánchez, Luis A. Bastida-Castro, José L. Torres-Cuevas, Julio A. Vasquez-Vasquez, Alejandra Diaz-Jarquin, Rafael Moreno-Novales, Joana Balderas-Juarez, Mauricio A. Salinas-Ramírez, Jose L. Hernández-Castillo, Erika K. Tenorio-Aguirre
Publikováno v:
Canadian Journal of Kidney Health and Disease, Vol 11 (2024)
Background: Acute kidney injury (AKI) is a frequent complication associated with severe COVID-19 and has been linked to increased mortality. While vaccination against SARS-CoV-2 has shown effectiveness in reducing severe COVID-19 outcomes, its impact
Externí odkaz:
https://doaj.org/article/a11df1fe8a9849919b9130a27277cb9b
Autor:
Gerardo E. Fabian‐Morales, Vianey Ordoñez‐Labastida, Froylan Garcia‐Martínez, Luis Montes‐Almanza, Juan C. Zenteno
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 10, Pp n/a-n/a (2024)
ABSTRACT Background Retinal dystrophies (RDs) are the most common cause of inherited blindness worldwide and are caused by genetic defects in about 300 different genes. While targeted next‐generation sequencing (NGS) has been demonstrated to be a r
Externí odkaz:
https://doaj.org/article/4f8c2030f5db48fdbf5b4b3d38238ac7
Autor:
Jacqueline Córdova‐Gallardo, Froylan David Martínez‐Sánchez, David Medina‐Julio, Martin Edgardo Rojano‐Rodríguez, Luz Sujey Romero‐Loera, Romina Vargas‐Agredano, Nahum Méndez‐Sánchez
Publikováno v:
JGH Open, Vol 8, Iss 9, Pp n/a-n/a (2024)
Abstract Background Obesity is a significant risk factor for metabolic‐associated steatotic liver disease (MASLD). The association between Helicobacter pylori (HP) infection and liver fibrosis has not been fully elucidated in patients with obesity
Externí odkaz:
https://doaj.org/article/2c0ea4435f994d6eb9a098bab8ed0512
Autor:
Aldo Torre, Froylan David Martínez‐Sánchez, Sofía Mercedes Narvaez‐Chávez, Mariana Ariel Herrera‐Islas, Carlos Alberto Aguilar‐Salinas, Jacqueline Córdova‐Gallardo
Publikováno v:
Immunity, Inflammation and Disease, Vol 12, Iss 7, Pp n/a-n/a (2024)
Abstract Background Pirfenidone has demonstrated significant anti‐inflammatory and antifibrotic effects in both animal models and some clinical trials. Its potential for antifibrotic activity positions it as a promising candidate for the treatment
Externí odkaz:
https://doaj.org/article/0193903825b8415cb79844f588b53bda
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:
Durga Praveen Meka, Melanie Richter, Tabitha Rücker, Hannah Voss, Anne Rissiek, Christoph Krisp, Nisha Hemandhar Kumar, Birgit Schwanke, Eugenio F. Fornasiero, Hartmut Schlüter, Froylan Calderon de Anda
Publikováno v:
STAR Protocols, Vol 5, Iss 1, Pp 102793- (2024)
Summary: Here, we present a protocol for differential multi-omic analyses of distinct cell types in the developing mouse cerebral cortex. We describe steps for in utero electroporation, subsequent flow-cytometry-based isolation of developing mouse co
Externí odkaz:
https://doaj.org/article/eee56e1f1edb44948be54c5032d54001
Autor:
Froylan D. Martínez-Sánchez, Héctor R. González-Sánchez, Joana Balderas-Juárez, Mauricio A. Salinas-Ramírez, Santiago Saenz-Ancira, Alejandra Diaz-Jarquin, Luis A. Ibarra-Santoyo, Juan C. Gonzalez-García, Erika K. Tenorio-Aguirre
Publikováno v:
Nefrología Latinoamericana, Vol 21, Iss 1 (2024)
Objective: Acute kidney injury (AKI) has been associated with adverse outcomes in patients with COVID-19. However, due to resource limitations across various centers, particularly in Latin America, the clinical course of AKI varies widely. Few data h
Externí odkaz:
https://doaj.org/article/3a0556efa3fe4de79dffe4250c9cd112
Autor:
Denisse Morales-Tovar, Froylan D. Martínez-Sánchez, Alejandro Gabutti-Thomas, Rodolfo Rivera-Martínez, Jacqueline Córdova-Gallardo
Publikováno v:
Case Reports in Gastrointestinal Medicine, Vol 2024 (2024)
Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu–Osler–Weber syndrome, is a vascular disorder of autosomal dominant etiology. The hallmark clinical feature is the presence of recurrent episodes of epistaxis in patients with vascul
Externí odkaz:
https://doaj.org/article/7156e4acb70b448695ddd124e0c88bec
Autor:
Froylan Sosa, Kyungjun Uh, Jéssica N Drum, Katy S Stoecklein, Kimberly M Davenport, M Sofia Ortega, Kiho Lee, Peter J Hansen
Publikováno v:
Reproduction and Fertility, Vol 4, Iss 2, Pp 1-10 (2023)
The hypothesis that colony-stimulating factor 2 (CSF2) plays a role in the preimplantation development of the bovine embryo was tested by evaluating consequences of inactivation of CSF2RA (the functional receptor in the embryo) for the development of
Externí odkaz:
https://doaj.org/article/02ff380e2510433ea817e7292a2dfc33