Zobrazeno 1 - 10
of 57
pro vyhledávání: '"José Suazo"'
Autor:
Ricardo A. Verdugo, Alex Di Genova, Luisa Herrera, Mauricio Moraga, Mónica Acuña, Soledad Berríos, Elena Llop, Carlos Y. Valenzuela, M. Leonor Bustamante, Dayhana Digman, Adriana Symon, Soledad Asenjo, Pamela López, Alejandro Blanco, José Suazo, Emmanuelle Barozet, Fresia Caba, Marcelo Villalón, Sergio Alvarado, Dante Cáceres, Katherine Salgado, Pilar Portales, Andrés Moreno-Estrada, Christopher R. Gignoux, Karla Sandoval, Carlos D. Bustamante, Celeste Eng, Scott Huntsman, Esteban G. Burchard, Nicolás Loira, Alejandro Maass, Lucía Cifuentes
Publikováno v:
Biological Research, Vol 53, Iss 1, Pp 1-11 (2020)
Abstract Background Current South American populations trace their origins mainly to three continental ancestries, i.e. European, Amerindian and African. Individual variation in relative proportions of each of these ancestries may be confounded with
Externí odkaz:
https://doaj.org/article/2ce97e1e592a4a30aefdab2ba01db8cd
Autor:
Luis Rodrigo Cataldo, José Suazo, Pablo Olmos, Carolina Bravo, José E. Galgani, Malin Fex, J. Alfredo Martínez, José L. Santos
Publikováno v:
Journal of Diabetes Research, Vol 2019 (2019)
Most peripheral serotonin (5-hydroxytryptamine (5HT)) is synthetized in the gut with platelets being its main circulating reservoir. 5HT is acting as a hormone in key organs to regulate glucose and lipid metabolism. However, the relation between plat
Externí odkaz:
https://doaj.org/article/3a2398784e2a47e3996a8ad87ac23fd6
Autor:
Susan V. Smalley, Yudith Preiss, José Suazo, Javier Andrés Vega, Isidora Angellotti, Carlos F. Lagos, Enzo Rivera, Karin Kleinsteuber, Javier Campion, J. Alfredo Martínez, Alberto Maiz, José Luis Santos
Publikováno v:
Genetics and Molecular Biology, Vol 38, Iss 1, Pp 30-36 (2015)
Cerebrotendinous Xanthomatosis (CTX), a rare lipid storage disorder, is caused by recessive loss-of-function mutations of the 27-sterol hydroxylase (CYP27A1), producing an alteration of the synthesis of bile acids, with an accumulation of cholestanol
Externí odkaz:
https://doaj.org/article/8c4aa20bed8740f3b713e55ad5915b7d
Autor:
Adolfo A. Paz, German A. Arenas, Sebastián Castillo-Galán, Estefanía Peñaloza, Gabriela Cáceres-Rojas, José Suazo, Emilio A. Herrera, Bernardo J. Krause
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 14, p 3474 (2019)
Cardiovascular risk associated with fetal growth restriction (FGR) could result from an early impaired vascular function. However, whether this effect results in premature vascular aging has not been addressed. We studied the ex vivo reactivity of ca
Externí odkaz:
https://doaj.org/article/df28b9da5cc143e094ef66eb7e090ce6
Publikováno v:
Revista Facultad de Odontología Universidad de Antioquia, Vol 24, Iss 1, Pp 110-120 (2012)
INTRODUCCIÓN: la fisura labio palatina no sindrómica, NSCLP (del inglés Nonsyndromic cleft lip and palate) es una de las malformaciones congénitas más frecuentes tanto en Chile como en el resto del mundo. Presenta un modo de herencia multifactor
Externí odkaz:
https://doaj.org/article/2ab5c5545fbc49669037b012b589dc9c
Publikováno v:
Genetics and Molecular Biology, Vol 31, Iss 3, Pp 639-642 (2008)
Nonsyndromic cleft lip/palate (NSCLP) is a congenital malformation with features of a complex genetic trait. Several studies have reported positive association and linkage between NSCLP and microsatellite markers in the 4q28-4q33 region particularly
Externí odkaz:
https://doaj.org/article/99a480d86aff45caae7d5adcfcc9ee02
Autor:
José Suazo, Carlos Salamanca, Patricio González-Hormazábal, Gabriela Cáceres-Rojas, Roberto Pantoja, Noemi Leiva, Rosa Pardo
Publikováno v:
Epigenomics. 14:987-993
Aim: To assess the association between PEMT variants and nonsyndromic cleft lip with or without cleft palate in Chile and the effects of these variants on global DNA methylation. Subjects & methods: The authors obtained genotypes for nine variants fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0259263375ca34d6ce8340a1a743ab73
https://doi.org/10.2217/epi-2022-0180
https://doi.org/10.2217/epi-2022-0180
Autor:
José Suazo, Carlos Salamanca, Gabriela Cáceres-Rojas, Patricio González-Hormazábal, Roberto Pantoja, Noemi Leiva, Rosa Pardo
Publikováno v:
Reproductive sciences (Thousand Oaks, Calif.). 29(10)
The aims of this study were to assess the association between polymorphisms within genes involved in vitamin B12 transport and nonsyndromic cleft lip with or without cleft palate (NSCL/P) and global DNA methylation in Chile. From 247 cases and 453 co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed6ab137e4e7a444e9027780e80814fe
https://pubmed.ncbi.nlm.nih.gov/35471549
https://pubmed.ncbi.nlm.nih.gov/35471549
Autor:
Noemí Leiva, Rosa Pardo, Gabriela Cáceres-Rojas, José Luis Santos, José Suazo, Roberto Pantoja, Bernardo J. Krause, Andrea S. Recabarren, Carlos Salamanca, Pamela A. Recabarren
Publikováno v:
Epigenomics. 12:1783-1791
Aim: To evaluate the risk of nonsyndromic orofacial clefts (NSOFCs) associated with LINE-1 methylation, as a marker of global DNA methylation, and the effect of MTHFR functional variants on this variable. Patients & methods: LINE-1 methylation was ev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b14e54ec3d146c5aa2723f1a627c45a5
https://doi.org/10.2217/epi-2020-0021
https://doi.org/10.2217/epi-2020-0021
Autor:
Andrea S. Recabarren, Noemí Leiva, José Suazo, Pamela A. Recabarren, Roberto Pantoja, Patricio Gonzalez-Hormazabal, Carlos Salamanca, Rosa Pardo
Publikováno v:
Pediatric Research. 89:1020-1025
Background The S-adenosyl-methionine (SAM) availability is crucial for DNA methylation, an epigenetic mechanism involved in nonsyndromic cleft lip with or without cleft palate (NSCL/P) expression. The aim of this study was to assess the association b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::792d81a9f8ced999650c64fca74b163a
https://doi.org/10.1038/s41390-020-0994-3
https://doi.org/10.1038/s41390-020-0994-3