Zobrazeno 1 - 10
of 37
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:
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
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:
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
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.
Uncommon Variants in FLG2 and NOD2 Are Associated with Atopic Dermatitis in the Ethiopian Population
Autor:
Sailan Wang, Julia K. Elmgren, Jesper Eisfeldt, Samina Asad, Marlene Ek, Kassahun Bilcha, Annisa Befekadu, Carl-Fredrik Wahlgren, Magnus Nordenskjöld, Fulya Taylan, Isabel Tapia-Paez, Maria Bradley
Publikováno v:
JID Innovations, Vol 4, Iss 4, Pp 100284- (2024)
Loss-of-function variants in the FLG gene have been identified as the strongest cause of susceptibility to atopic dermatitis (AD) in Europeans and Asians. However, very little is known about the genetic etiology behind AD in African populations, wher
Externí odkaz:
https://doaj.org/article/75bdc359543b4bccb2e07264566ac53b
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
Autor:
Sailan Wang, Pernilla Nikamo, Leena Laasonen, Bjorn Gudbjornsson, Leif Ejstrup, Lars Iversen, Ulla Lindqvist, Jessica J Alm, Jesper Eisfeldt, Xiaowei Zheng, Sergiu-Bogdan Catrina, Fulya Taylan, Raquel Vaz, Mona Ståhle, Isabel Tapia-Paez
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 3, Pp 596-615 (2024)
Abstract Psoriatic arthritis mutilans (PAM) is the rarest and most severe form of psoriatic arthritis, characterized by erosions of the small joints and osteolysis leading to joint disruption. Despite its severity, the underlying mechanisms are unkno
Externí odkaz:
https://doaj.org/article/d7a494fdd8c144ae87005d0481ad98df