Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Isabel Tapia Páez"'
Autor:
Andrea Bieder, Gayathri Chandrasekar, Arpit Wason, Steffen Erkelenz, Jay Gopalakrishnan, Juha Kere, Isabel Tapia-Páez
Publikováno v:
BMC Molecular and Cell Biology, Vol 24, Iss 1, Pp 1-11 (2023)
Abstract Background DYX1C1 (DNAAF4) and DCDC2 are two of the most replicated dyslexia candidate genes in genetic studies. They both have demonstrated roles in neuronal migration, in cilia growth and function and they both are cytoskeletal interactors
Externí odkaz:
https://doaj.org/article/5a629c5f0dd84427b3b6480a114b3a49
Autor:
Andrea Bieder, Elisabet Einarsdottir, Hans Matsson, Harriet E. Nilsson, Jesper Eisfeldt, Anca Dragomir, Martin Paucar, Tobias Granberg, Tie-Qiang Li, Anna Lindstrand, Juha Kere, Isabel Tapia-Páez
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
Abstract Background Developmental dyslexia (DD) is a neurodevelopmental learning disorder with high heritability. A number of candidate susceptibility genes have been identified, some of which are linked to the function of the cilium, an organelle re
Externí odkaz:
https://doaj.org/article/5544082e59974e9a9eb410d7ba08276a
Autor:
Andrea Bieder, Gayathri Chandrasekar, Arpit Wason, Steffen Erkelenz, Jay Gopalakrishnan, Isabel Tapia-Páez, Juha Kere
Background: DYX1C1 (DNAAF4) and DCDC2 are two of the most replicated dyslexia candidate genes in genetic studies. They both have demonstrated roles in neuronal migration, in cilia growth and function and they both are cytoskeletal interactors. In add
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba4a5669109418a0ef9a47d7f6b891da
https://doi.org/10.21203/rs.3.rs-2251941/v1
https://doi.org/10.21203/rs.3.rs-2251941/v1
Autor:
Avinash Padhi, Rokeya Sultana Rekha, Lisa Benrejdal, Marijke Elise Grundeken, Magda Lourda, Marcus Ehrström, Kilian Eyerich, Isabel Tapia Páez, Emma K. Johansson, Maria Bradley, Peter Bergman, Josefin Lysell
Publikováno v:
Journal of Investigative Dermatology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28779a8852fa4a7e4f78441ee587fdbb
https://doi.org/10.1016/j.jid.2022.12.012
https://doi.org/10.1016/j.jid.2022.12.012
Autor:
Samina Asad, Isabel Tapia-Páez, Andrea Montano Montes, Carl-Fredrik Wahlgren, Kassahun D. Bilcha, Magnus Nordenskjöld, Maria Bradley
Publikováno v:
Acta Dermato-Venereologica, Vol 99, Iss 1, Pp 101-102 (2018)
Externí odkaz:
https://doaj.org/article/29291ca9472f483787a84d451de87573
Autor:
Isabel Tapia-Páez, Shintaro Katayama, Masahito Yoshihara, Kaarel Krjutškov, Anna Falk, Juha Kere, Andrea Bieder
Publikováno v:
Molecular Neurobiology
Developmental dyslexia (DD) is a neurodevelopmental condition with complex genetic mechanisms. A number of candidate genes have been identified, some of which are linked to neuronal development and migration and to ciliary functions. However, express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e57c2b3c956fb5de87044ee0466cae3
https://doi.org/10.1007/s12035-020-01905-6
https://doi.org/10.1007/s12035-020-01905-6
Autor:
Pontus Höjer, A. Srivastava, Enikö Sonkoly, Magnus Nordenskjöld, Rapolas Spalinskas, Carl-Fredrik Wahlgren, Kyu-Han Kim, Pelin Sahlén, Anandashankar Anil, Isabel Tapia-Páez, Mona Ståhle, Fulya Taylan, Samina Asad, Jesper Eisfeldt, Maria Bradley, Pernilla Nikamo, Otto Bergman, Kunal Das Mahapatra, Andor Pivarcsi, Anaya Mukherjee
Background Hundreds of variants associated with atopic dermatitis (AD) and psoriasis, 2 common inflammatory skin disorders, have previously been discovered through genome-wide association studies (GWASs). The majority of these variants are in noncodi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e75e7fa85dddf9cb6eeb6984fce991bd
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-441672
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-441672
Publikováno v:
PLoS ONE, Vol 8, Iss 5, p e63123 (2013)
DYX1C1, a susceptibility gene for dyslexia, encodes a tetratricopeptide repeat domain containing protein that has been implicated in neuronal migration in rodent models. The developmental role of this gene remains unexplored. To understand the biolog
Externí odkaz:
https://doaj.org/article/caf5ec659bdc48c8906406028d58931a
Autor:
Martin Paucar, Anca Dragomir, Tie-Qiang Li, Harriet Nilsson, Elisabet Einarsdottir, Juha Kere, Anna Lindstrand, Tobias Granberg, Hans Matsson, Andrea Bieder, Jesper Eisfeldt, Isabel Tapia-Páez
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-9 (2020)
BackgroundDevelopmental dyslexia (DD) is a neurodevelopmental learning disorder with high heritability. A number of candidate susceptibility genes have been identified, some of which are linked to the function of the cilium, an organelle regulating l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cb27fa8c2ee5534f56ea5996d8e28c4
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413235
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413235
Autor:
Satu Massinen, Marie-Estelle Hokkanen, Hans Matsson, Kristiina Tammimies, Isabel Tapia-Páez, Vanina Dahlström-Heuser, Juha Kuja-Panula, Jan Burghoorn, Kristian E Jeppsson, Peter Swoboda, Myriam Peyrard-Janvid, Rune Toftgård, Eero Castrén, Juha Kere
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e20580 (2011)
DCDC2 is one of the candidate susceptibility genes for dyslexia. It belongs to the superfamily of doublecortin domain containing proteins that bind to microtubules, and it has been shown to be involved in neuronal migration. We show that the Dcdc2 pr
Externí odkaz:
https://doaj.org/article/ddfd00b63e7e452f9a300c2d098793a9