Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Maricela García-Castañeda"'
Autor:
Antonio Michelucci, Simona Boncompagni, Laura Pietrangelo, Maricela García-Castañeda, Takahiro Takano, Sundeep Malik, Robert T Dirksen, Feliciano Protasi
Publikováno v:
eLife, Vol 8 (2019)
Exercise promotes the formation of intracellular junctions in skeletal muscle between stacks of sarcoplasmic reticulum (SR) cisternae and extensions of transverse-tubules (TT) that increase co-localization of proteins required for store-operated Ca2+
Externí odkaz:
https://doaj.org/article/11fb6153e0024e5d8788476c889af181
Autor:
Yu Seby Chen, Maricela Garcia-Castañeda, Maria Charalambous, Daniela Rossi, Vincenzo Sorrentino, Filip Van Petegem
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-12 (2024)
Abstract Ryanodine Receptor isoform 3 (RyR3) is a large ion channel found in the endoplasmic reticulum membrane of many different cell types. Within the hippocampal region of the brain, it is found in dendritic spines and regulates synaptic plasticit
Externí odkaz:
https://doaj.org/article/99a0a0c3b3b549beb8302f26252aaaaa
Autor:
Maricela García-Castañeda, Luz del Carmen Camacho-Castillo, Patrick Mailloux-Salinas, Guillermo Avila, Marco Antonio Mártinez-Ávila, Erick Benjamín Ríos-Pérez, Ma. Dolores Bello-Sanchez, Guadalupe Bravo, Maritza Mayorga-Luna, Norma L. Gómez-Viquez, Karla Carvajal, Jaime Balderas-Villalobos, Julio Altamirano
Publikováno v:
Archives of Physiology and Biochemistry. :1-13
We investigated how oxidative stress (OS) alters Ca2+ handling in ventricular myocytes in early metabolic syndrome (MetS) in sucrose-fed rats. The effects of N-acetyl cysteine (NAC) or dl-Dithiothreitol (DTT) on systolic Ca2+ transients (SCaTs), dias
Publikováno v:
The Journal of general physiology. 154(9)
Duchenne muscular dystrophy (DMD), an X-linked disorder caused by loss-of-function mutations in the dystrophin gene, is characterized by progressive muscle degeneration and weakness. Enhanced store-operated Ca2+ entry (SOCE), a Ca2+ influx mechanism
Autor:
Norma Leticia, Gómez-Viquez, Jaime, Balderas-Villalobos, Ma Dolores, Bello-Sánchez, Maritza, Mayorga-Luna, Patrick, Mailloux-Salinas, Maricela, García-Castañeda, Erick Benjamín, Ríos-Pérez, Marco Antonio, Mártinez-Ávila, Luz Del Carmen, Camacho-Castillo, Guadalupe, Bravo, Guillermo, Ávila, Julio, Altamirano, Karla, Carvajal
Publikováno v:
Archives of physiology and biochemistry.
We investigated how oxidative stress (OS) alters Ca
Autor:
Maricela García-Castañeda, Guillermo Avila, Teresa Mancilla-Percino, Juan A.M. De La Rosa, Takuya Nishigaki, Juan Carlos Gomora
Publikováno v:
Molecular pharmacology. 98(3)
Amino acid-derived isoindolines are synthetic compounds that were created with the idea of investigating their biological actions. The amino acid moiety was included on the grounds that it may help to avoid toxic effects. Recently, the isoindoline MD
Autor:
Angel Zarain-Herzberg, Ana V. Vega, Bulmaro Cisneros, Guillermo Avila, María Guadalupe Montiel-Jaen, Maricela García-Castañeda, Rocío Rodríguez
Publikováno v:
The Journal of Physiology. 595:4167-4187
Key points Mutations in the gene encoding poly(A)-binding protein nuclear 1 (PABPN1) result in oculopharyngeal muscular dystrophy (OPMD). This disease is of late-onset, but the underlying mechanism is unclear. Ca2+ stimulates muscle growth and contra
Author response: Transverse tubule remodeling enhances Orai1-dependent Ca2+ entry in skeletal muscle
Autor:
Laura Pietrangelo, Robert T. Dirksen, Feliciano Protasi, Antonio Michelucci, Sundeep Malik, Simona Boncompagni, Maricela García-Castañeda, Takahiro Takano
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb51a2fdd3a5bea57853b469f5bd47a8
https://doi.org/10.7554/elife.47576.020
https://doi.org/10.7554/elife.47576.020
Autor:
Antonio Michelucci, Robert T. Dirksen, Stephanie Brennan, Lan Wei LaPierre, Linda Groom, Maricela García-Castañeda, Nesrin Sabha, James J. Dowling, Sundeep Malik
Publikováno v:
Hum Mol Genet
Ryanodine receptor type I (RYR1)-related myopathies (RYR1 RM) are a clinically and histopathologically heterogeneous group of conditions that represent the most common subtype of childhood onset non-dystrophic muscle disorders. There are no treatment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42fb87047f11ba1ffd6da4656376fe92
http://hdl.handle.net/11391/1517029
http://hdl.handle.net/11391/1517029
Autor:
Maricela García-Castañeda, Adrián Monsalvo-Villegas, Guillermo Avila, Erick Benjamín Ríos-Pérez
Publikováno v:
Pflügers Archiv - European Journal of Physiology. 468:1823-1835
It is widely accepted that aldosterone induces atrial fibrillation (AF) by promoting structural changes, but its effects on the function of primary atrial myocytes remain unknown. We have investigated this point in adult rat atrial myocytes, chronica