Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Edyta Stasiek"'
Autor:
Esther R Berko, Masako Suzuki, Faygel Beren, Christophe Lemetre, Christine M Alaimo, R Brent Calder, Karen Ballaban-Gil, Batya Gounder, Kaylee Kampf, Jill Kirschen, Shahina B Maqbool, Zeineen Momin, David M Reynolds, Natalie Russo, Lisa Shulman, Edyta Stasiek, Jessica Tozour, Maria Valicenti-McDermott, Shenglong Wang, Brett S Abrahams, Joseph Hargitai, Dov Inbar, Zhengdong Zhang, Joseph D Buxbaum, Sophie Molholm, John J Foxe, Robert W Marion, Adam Auton, John M Greally
Publikováno v:
PLoS Genetics, Vol 10, Iss 5, p e1004402 (2014)
DNA mutational events are increasingly being identified in autism spectrum disorder (ASD), but the potential additional role of dysregulation of the epigenome in the pathogenesis of the condition remains unclear. The epigenome is of interest as a pos
Externí odkaz:
https://doaj.org/article/a803dd8795744243ae732bdcac7b9739
Autor:
Andrew S McLellan, Richard Sandstrom, Frederick Agyiri, Reid F. Thompson, Edyta Stasiek, Kevin W. Lau, R. Scott Hansen, Marien Pascual, Masako Suzuki, John A. Stamatoyannopoulos, John M. Greally, Melissa Fazzari, Jacob L. Glass, Qiang Jing, María Paz Ramos, Mayumi Oda
Heterochromatin is believed to be associated with increased levels of cytosine methylation. With the recent availability of genome-wide, high-resolution molecular data reflecting chromatin organization and methylation, such relationships can be explo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc757200bc2bc59dffc7c325a5e847eb
https://europepmc.org/articles/PMC3205568/
https://europepmc.org/articles/PMC3205568/
Autor:
Eli Hatchwell, Batbayar Khulan, Roland Green, Quan Chen, Kenny Ye, Maria E. Figueroa, Masako Suzuki, Ari Melnick, Todd Richmond, Rebecca R. Selzer, John M. Greally, Edyta Stasiek, Cristina Montagna, Reid F. Thompson, Jacob L. Glass, Melissa Fazzari
Publikováno v:
Batbayar, K, Thompson, R F, Ye, K, Fazzari, M J, Suzuki, M, Stasiek, E, Figueroa, M E, Glass, J L, Chen, Q, Montagna, C, Hatchwell, E, Selzer, R R, Richmond, T A, Green, R D, Melnick, A & Greally, J M 2006, ' Comparative isoschizomer profiling of cytosine methylation : the HELP assay ', Genome Research, vol. 16, no. 8, pp. 1046-55 . https://doi.org/10.1101/gr.5273806
The distribution of cytosine methylation in 6.2 Mb of the mouse genome was tested using cohybridization of genomic representations from a methylation-sensitive restriction enzyme and its methylation-insensitive isoschizomer. This assay, termed HELP (
Autor:
Mihaela Stefan, Richard Longnecker, Jing Hua Chai, Kathryn Claiborn, Edyta Stasiek, Tohru Ohta, Robert D. Nicholls, John M. Greally
Publikováno v:
BMC Genomics, Vol 6, Iss 1, p 157 (2005)
BMC Genomics
BMC Genomics
Background Prader-Willi and Angelman syndrome (PWS and AS) patients typically have an ~5 Mb deletion of human chromosome 15q11-q13, of opposite parental origin. A mouse model of PWS and AS has a transgenic insertion-deletion (TgPWS/TgAS) of chromosom
Autor:
Sophie Molholm, Zeineen Momin, Joseph D. Buxbaum, Karen Ballaban-Gil, Faygel Beren, Dov Inbar, Joseph Hargitai, John J. Foxe, Adam Auton, Masako Suzuki, Zhengdong D. Zhang, Jill Kirschen, Christophe Lemetre, John M. Greally, Robert W. Marion, David Reynolds, Maria Valicenti-McDermott, Brett S. Abrahams, Batya Gounder, Natalie Russo, Shahina Maqbool, Shenglong Wang, Jessica Tozour, Edyta Stasiek, Christine M. Alaimo, Kaylee Kampf, Lisa H. Shulman, R. Brent Calder, Esther R. Berko
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 10, Iss 5, p e1004402 (2014)
PLoS Genetics, Vol 10, Iss 5, p e1004402 (2014)
DNA mutational events are increasingly being identified in autism spectrum disorder (ASD), but the potential additional role of dysregulation of the epigenome in the pathogenesis of the condition remains unclear. The epigenome is of interest as a pos