Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Cesar, Trigo"'
Autor:
Ioannis Angelopoulos, Cesar Trigo, Maria-Ignacia Ortuzar, Jimena Cuenca, Claudia Brizuela, Maroun Khoury
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-15 (2022)
Abstract The main goal of regenerative endodontics procedures (REPs) is to revitalize teeth by the regeneration of healthy dental pulp. In this study, we evaluated the potential of combining a natural and accessible biomaterial based on Platelet Poor
Externí odkaz:
https://doaj.org/article/02422ff717da4cc8a826ebcaf2b410b0
Autor:
Carla Verônica Cesar Trigo
Publikováno v:
Revista Interinstitucional Artes de Educar, Vol 6, Iss 1, Pp 360-381 (2020)
O presente trabalho desenvolve um estudo sobre o ensino da Dança na Educação Infantil. O objetivo dessa pesquisa é o de compreender o fenômeno do protagonismo infantil no ensino da Dança e suas implicações na prática pedagógica. Seu campo d
Externí odkaz:
https://doaj.org/article/eb288c6a08e44b58abf0c9e216c24492
Autor:
Emma K. Baker, Marta Arpone, Solange Aliaga Vera, Lesley Bretherton, Alexandra Ure, Claudine M. Kraan, Minh Bui, Ling Ling, David Francis, Matthew F. Hunter, Justine Elliott, Carolyn Rogers, Michael J. Field, Jonathan Cohen, Lorena Santa Maria, Victor Faundes, Bianca Curotto, Paulina Morales, Cesar Trigo, Isabel Salas, Angelica M. Alliende, David J. Amor, David E. Godler
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-15 (2019)
Abstract Background Fragile X syndrome (FXS) is a common cause of intellectual disability and autism spectrum disorder (ASD) usually associated with a CGG expansion, termed full mutation (FM: CGG ≥ 200), increased DNA methylation of the FMR1 promot
Externí odkaz:
https://doaj.org/article/e05c1a167cbd4ce9a6910a82c9dd4958
Autor:
Emma K. Baker, Marta Arpone, Solange M. Aliaga, Lesley Bretherton, Claudine M. Kraan, Minh Bui, Howard R. Slater, Ling Ling, David Francis, Matthew F. Hunter, Justine Elliott, Carolyn Rogers, Michael Field, Jonathan Cohen, Kim Cornish, Lorena Santa Maria, Victor Faundes, Bianca Curotto, Paulina Morales, Cesar Trigo, Isabel Salas, Angelica M. Alliende, David J. Amor, David E. Godler
Publikováno v:
Molecular Autism, Vol 10, Iss 1, Pp 1-13 (2019)
Abstract Background Fragile X syndrome (FXS) is a common monogenic cause of intellectual disability with autism features. While it is caused by loss of the FMR1 product (FMRP), mosaicism for active and inactive FMR1 alleles, including alleles termed
Externí odkaz:
https://doaj.org/article/c8c8fc51efc34be5844911b0781f350c
Autor:
Emma K. Baker, Marta Arpone, Minh Bui, Claudine M. Kraan, Ling Ling, David Francis, Mathew F. Hunter, Carolyn Rogers, Michael J. Field, Lorena Santa María, Víctor Faundes, Bianca Curotto, Paulina Morales, Cesar Trigo, Isabel Salas, Angelica M. Alliende, David J. Amor, David E. Godler
Publikováno v:
American journal of medical genetics. Part AREFERENCES.
Fragile X syndrome (FXS) is caused by hypermethylation of the FMR1 promoter due to the full mutation expansion (full mutation [FM]: CGG ≥ 200 repeats) and silencing of FMR1. Assessment of mosaicism for active-unmethylated alleles has prognostic uti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fe1aad712bb4a2e2b8f25fd39879e43
https://pubmed.ncbi.nlm.nih.gov/36349505
https://pubmed.ncbi.nlm.nih.gov/36349505
Publikováno v:
BioTechniques, Vol 54, Iss 4, Pp 191-196 (2013)
Plasma membrane receptors, transporters, and ion channel molecules are often found as oligomeric structures that participate in signaling cascades essential for cell survival. Different states of protein oligomerization may play a role in functional
Externí odkaz:
https://doaj.org/article/aab3009d94214644bfdba2895e6d93da
Autor:
Solange Aliaga Vera, Emma Baker, Víctor Faundes, Michael Field, Matthew F. Hunter, Minh Bui, Bianca Curotto, Isabel Salas, Ling Ling, Jonathan Cohen, Angelica M. Alliende, Lorena Santa María, Justine Elliott, Marta Arpone, Claudine Kraan, Alexandra Ure, Cesar Trigo, David J. Amor, David E. Godler, Carolyn Rogers, David Francis, Paulina Morales, Lesley Bretherton
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 11, Iss 1, Pp 1-15 (2019)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders
BackgroundFragile X syndrome (FXS) is a common cause of intellectual disability and autism spectrum disorder (ASD) usually associated with a CGG expansion, termed full mutation (FM: CGG ≥ 200), increased DNA methylation of theFMR1promoter and silen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06fb46f1ee7d1f6a9a60724f73700ec8
https://doaj.org/article/e05c1a167cbd4ce9a6910a82c9dd4958
https://doaj.org/article/e05c1a167cbd4ce9a6910a82c9dd4958
Autor:
Michael Field, Isabel Salas, Jonathan Cohen, David Francis, Carolyn Rogers, Justine Elliott, Lesley Bretherton, David E. Godler, Paulina Morales, Claudine Kraan, Bianca Curotto, Lorena Santa María, David J. Amor, Marta Arpone, Emma Baker, Víctor Faundes, Ling Ling, Matthew F. Hunter, Solange M. Aliaga, Minh Bui, Howard R. Slater, Kim Cornish, Cesar Trigo, Angelica M. Alliende
Publikováno v:
Molecular Autism, Vol 10, Iss 1, Pp 1-13 (2019)
Molecular Autism
Molecular Autism
Background Fragile X syndrome (FXS) is a common monogenic cause of intellectual disability with autism features. While it is caused by loss of the FMR1 product (FMRP), mosaicism for active and inactive FMR1 alleles, including alleles termed premutati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd7cd09314434dac903d2a628e224719
http://link.springer.com/article/10.1186/s13229-019-0271-7
http://link.springer.com/article/10.1186/s13229-019-0271-7
Autor:
Michael Field, Lesley Bretherton, Víctor Faundes, Ling Ling, Cesar Trigo, Matthew F. Hunter, David J. Amor, Paulina Morales, Minh Bui, Claudine Kraan, Bianca Curotto, Emma Baker, Lorena Santa María, Marta Arpone, Angelica M. Alliende, Isabel Salas, Jonathan Cohen, Alexandra Ure, David E. Godler, Carolyn Rogers
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
Fragile X syndrome (FXS) is caused by a hypermethylated full mutation (FM) expansion with ≥ 200 CGG repeats, and a decrease in FMR1 mRNA and its protein. However, incomplete silencing from FM alleles has been associated with more severe autism feat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78985afbbb152928de5a65b772859637
https://doi.org/10.1038/s41598-020-68465-6
https://doi.org/10.1038/s41598-020-68465-6
Autor:
Emma K, Baker, Marta, Arpone, Claudine, Kraan, Minh, Bui, Carolyn, Rogers, Michael, Field, Lesley, Bretherton, Ling, Ling, Alexandra, Ure, Jonathan, Cohen, Matthew F, Hunter, Lorena, Santa María, Victor, Faundes, Bianca, Curotto, Paulina, Morales, Cesar, Trigo, Isabel, Salas, Angelica, Alliende, David J, Amor, David E, Godler
Publikováno v:
Scientific Reports
Fragile X syndrome (FXS) is caused by a hypermethylated full mutation (FM) expansion with ≥ 200 CGG repeats, and a decrease in FMR1 mRNA and its protein. However, incomplete silencing from FM alleles has been associated with more severe autism feat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc945d7fca73a130f3de8589554b16ff
https://pubmed.ncbi.nlm.nih.gov/32678152
https://pubmed.ncbi.nlm.nih.gov/32678152