Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Emma K. Baker"'
Autor:
Malihe Safari, Leila Mahmoudi, Emma K. Baker, Ghodratollah Roshanaei, Ramazan Fallah, Ali Shahnavaz, Mohammad Asghari-Jafarabadi
Publikováno v:
The Turkish Journal of Gastroenterology, Vol 34, Iss 7, Pp 736-746 (2023)
Externí odkaz:
https://doaj.org/article/f442c5c4630a42fdb7cae6b7ac81fb0e
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, David E. Godler, Minh Bui, Chriselle Hickerton, Carolyn Rogers, Mike Field, David J. Amor, Lesley Bretherton
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 10, Iss 1, Pp 1-8 (2018)
Abstract Background Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are neurodevelopmental disorders that are caused by abnormal expression of imprinted genes in the 15q11-13 region. Dysregulation of genes located in this region has been propo
Externí odkaz:
https://doaj.org/article/6d1be37a99cf4a3fb0b6ce2764b65451
Autor:
Michael Field, Tracy Dudding-Byth, Marta Arpone, Emma K. Baker, Solange M. Aliaga, Carolyn Rogers, Chriselle Hickerton, David Francis, Dean G. Phelan, Elizabeth E. Palmer, David J. Amor, Howard Slater, Lesley Bretherton, Ling Ling, David E. Godler
Publikováno v:
International Journal of Molecular Sciences, Vol 20, Iss 16, p 3907 (2019)
Although fragile X syndrome (FXS) is caused by a hypermethylated full mutation (FM) expansion with ≥200 cytosine-guanine-guanine (CGG) repeats, and a decrease in FMR1 mRNA and its protein (FMRP), incomplete silencing has been associated with more s
Externí odkaz:
https://doaj.org/article/62efb1f2e5e6435a990c53fdfece87ff
Publikováno v:
Frontiers in Psychology, Vol 7 (2016)
Research with adults and older children indicates that verb biases are strong influences on listeners’ interpretations when processing sentences, but they can be overruled. In this paper we ask two questions: (i) are children with ASD who are high
Externí odkaz:
https://doaj.org/article/b4cd4eb07b384cccb26c2c6a60c8c5d8
Autor:
ShuhYing Tan, Chacko Joseph, Alistair M. Chalk, Jean Hendy, Stewart Fabb, Kelli Schleibs, Samuel C. Lee, Gavin Tjin, Clea S. Grace, Vinodini Madugalle, Monique F. Smeets, Ana C. Maluenda, Kim L. Rice, Emma K. Baker, Harshal Nandurkar, Christopher I. Slape, Michael W Parker, Ashwin Unnikrishnan, Ghulam J. Mufti, Magnus Tobiasson, Eva Hellstrom-Lindberg, John E. Pimanda, Lorraine J. Gudas, Jessica K. Holien, Carl R. Walkley, Meaghan Wall, Louise E. Purton
The homeobox gene,Hoxa1, has two different isoforms generated by alternative splicing: a full-length homeodomain-containingHoxa1(Hoxa1-FL), and a truncatedHoxa1(Hoxa1-T), that lacks the homeodomain. Oncoretroviral overexpression of wildtypeHoxa1cDNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70e33ff44b2fdccd0e106a5dee92ae00
https://doi.org/10.1101/2023.04.24.538176
https://doi.org/10.1101/2023.04.24.538176
Autor:
Carl R. Walkley, Kaylene J. Simpson, Michael A. Dyer, David C.S. Huang, Chris Burns, Andrew C.W. Zannettino, Piyush B. Madhamshettiwar, Jayesh Desai, Anthony J. Mutsaers, Åsa Karlström, Kurt Lackovic, Scott Taylor, Alistair M. Chalk, Cathryn M. Gould, Anang A. Shelat, Amos Loh, Elizabeth Stewart, Soo-San Wan, Emma K. Baker, Ankita Gupte
Purpose: Osteosarcoma is the most common cancer of bone occurring mostly in teenagers. Despite rapid advances in our knowledge of the genetics and cell biology of osteosarcoma, significant improvements in patient survival have not been observed. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::038b0bc2ae54a3ccfed107284bf17a8c
https://doi.org/10.1158/1078-0432.c.6523853.v1
https://doi.org/10.1158/1078-0432.c.6523853.v1
Autor:
Carl R. Walkley, Kaylene J. Simpson, Michael A. Dyer, David C.S. Huang, Chris Burns, Andrew C.W. Zannettino, Piyush B. Madhamshettiwar, Jayesh Desai, Anthony J. Mutsaers, Åsa Karlström, Kurt Lackovic, Scott Taylor, Alistair M. Chalk, Cathryn M. Gould, Anang A. Shelat, Amos Loh, Elizabeth Stewart, Soo-San Wan, Emma K. Baker, Ankita Gupte
Supplemental Material and Methods, Table 1, and Figures 1-7. Supplemental Table 1 - Primer Sequences used for qPCR. Supplemental Figure 1 - Suppressors of doxorubicin induced cell death from siRNA screen. Supplemental Figure 2 - Response to Spliceost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cc1106dccb2b6c4fd3769199c668b33
https://doi.org/10.1158/1078-0432.22458170.v1
https://doi.org/10.1158/1078-0432.22458170.v1
Autor:
Antony Kaspi, Michael S. Hildebrand, Victoria E. Jackson, Ruth Braden, Olivia van Reyk, Tegan Howell, Simone Debono, Mariana Lauretta, Lottie Morison, Matthew J. Coleman, Richard Webster, David Coman, Himanshu Goel, Mathew Wallis, Gabriel Dabscheck, Lilian Downie, Emma K. Baker, Bronwyn Parry-Fielder, Kirrie Ballard, Eva Harrold, Shaun Ziegenfusz, Mark F. Bennett, Erandee Robertson, Longfei Wang, Amber Boys, Simon E. Fisher, David J. Amor, Ingrid E. Scheffer, Melanie Bahlo, Angela T. Morgan
Publikováno v:
Molecular Psychiatry, 28, 4, pp. 1664-1666
Molecular Psychiatry, 28, 1664-1666
Molecular Psychiatry, 28, 1664-1666
Contains fulltext : 293730.pdf (Publisher’s version ) (Open Access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::059b5e06128141f777393c091ff9582e