Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Elisabet, Einarsdottir"'
Autor:
Xuan Li, Suvratha Jayaprasad, Elisabet Einarsdottir, Steven J. B. Cooper, Alexander Suh, Takeshi Kawakami, Octavio Manuel Palacios-Gimenez
Publikováno v:
Scientific Data, Vol 11, Iss 1, Pp 1-7 (2024)
Abstract Morabine grasshoppers in the Vandiemenella viatica species group, which show karyotype diversity, have been studied for their ecological distribution and speciation in relation to their genetic and chromosomal diversity. They are good models
Externí odkaz:
https://doaj.org/article/baa92806f56e485c873deb0c118bdc92
Autor:
Hao Yu, Anas M Khanshour, Aki Ushiki, Nao Otomo, Yoshinao Koike, Elisabet Einarsdottir, Yanhui Fan, Lilian Antunes, Yared H Kidane, Reuel Cornelia, Rory R Sheng, Yichi Zhang, Jimin Pei, Nick V Grishin, Bret M Evers, Jason Pui Yin Cheung, John A Herring, Chikashi Terao, You-qiang Song, Christina A Gurnett, Paul Gerdhem, Shiro Ikegawa, Jonathan J Rios, Nadav Ahituv, Carol A Wise
Publikováno v:
eLife, Vol 12 (2024)
Adolescent idiopathic scoliosis (AIS) is a common and progressive spinal deformity in children that exhibits striking sexual dimorphism, with girls at more than fivefold greater risk of severe disease compared to boys. Despite its medical impact, the
Externí odkaz:
https://doaj.org/article/008395c97b104a1f9a8bdc58a295796f
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:
Shintaro Katayama, Tiina Skoog, Cilla Söderhäll, Elisabet Einarsdottir, Kaarel Krjutškov, Juha Kere
Publikováno v:
BMC Bioinformatics, Vol 20, Iss 1, Pp 1-9 (2019)
Abstract Background Standard RNAseq methods using bulk RNA and recent single-cell RNAseq methods use DNA barcodes to identify samples and cells, and the barcoded cDNAs are pooled into a library pool before high throughput sequencing. In cases of sing
Externí odkaz:
https://doaj.org/article/043e8dac8a1a436db127b1c2770db1c5
Autor:
Elisabet Einarsdottir, Minna Pekkinen, Kaarel Krjutškov, Shintaro Katayama, Juha Kere, Outi Mäkitie, Heli Viljakainen
Publikováno v:
Endocrine Connections, Vol 8, Iss 5, Pp 559-570 (2019)
Objective: The effect of vitamin D at the transcriptome level is poorly understood, and furthermore, it is unclear if it differs between obese and normal-weight subjects. The objective of the study was to explore the transcriptome effects of vitamin
Externí odkaz:
https://doaj.org/article/3c0c7d5a02e64632a6ad5d4f020333ca
Autor:
Ulrika Käck, Elisabet Einarsdottir, Marianne van Hage, Anna Asarnoj, Anna James, Anna Nopp, Kaarel Krjutškov, Shintaro Katayama, Juha Kere, Gunnar Lilja, Cilla Söderhäll, Jon R. Konradsen
Publikováno v:
ERJ Open Research, Vol 7, Iss 2 (2021)
Background The clinical presentation of children sensitised to dog dander varies from asymptomatic to severe allergic airway disease, but the genetic mechanisms underlying these differences are not clear. The objective of the present study was to inv
Externí odkaz:
https://doaj.org/article/21eaab7f46a446e2a430db5e661057c9
Autor:
Liisa Harjama, Kaisa Kettunen, Outi Elomaa, Elisabet Einarsdottir, Hannele Heikkilä, Sirpa Kivirikko, Katriina Lappalainen, Janna Saarela, Caroline Alby, Annamari Ranki, Juha Kere, Smail Hadj-Rabia, Katariina Hannula-Jouppi
Publikováno v:
Acta Dermato-Venereologica, Vol 100, Iss 4, p adv00060 (2020)
Abstract is missing (Short communication)
Externí odkaz:
https://doaj.org/article/ff1f51c7a9b1440c8ba97096aa58c54d
Autor:
Salla Keskitalo, Emma Haapaniemi, Elisabet Einarsdottir, Kristiina Rajamäki, Hannele Heikkilä, Mette Ilander, Minna Pöyhönen, Ekaterina Morgunova, Kati Hokynar, Sonja Lagström, Sirpa Kivirikko, Satu Mustjoki, Kari Eklund, Janna Saarela, Juha Kere, Mikko R. J. Seppänen, Annamari Ranki, Katariina Hannula-Jouppi, Markku Varjosalo
Publikováno v:
Frontiers in Immunology, Vol 10 (2019)
Upon binding to pathogen or self-derived cytosolic nucleic acids cyclic GMP-AMP synthase (cGAS) triggers the production of cGAMP that further activates transmembrane protein STING. Upon activation STING translocates from ER via Golgi to vesicles. Mon
Externí odkaz:
https://doaj.org/article/775d1ce795a544fdb1edecb38e84d4c0
Autor:
Mahmood F. Bhutta, Jane Lambie, Lindsey Hobson, Anuj Goel, Lena Hafrén, Elisabet Einarsdottir, Petri S. Mattila, Martin Farrall, Steve Brown, Martin J. Burton
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Abstract Chronic otitis media with effusion (COME) is the most common cause of hearing loss in children, and known to have high heritability. Mutant mouse models have identified Fbxo11, Evi1, Tgif1, and Nisch as potential risk loci. We recruited chil
Externí odkaz:
https://doaj.org/article/4e3ad4f89c544c7ca34f1dfdf0d95724
Autor:
Janne Purhonen, Jayasimman Rajendran, Matthias Mörgelin, Kristiina Uusi-Rauva, Shintaro Katayama, Kaarel Krjutskov, Elisabet Einarsdottir, Vidya Velagapudi, Juha Kere, Matti Jauhiainen, Vineta Fellman, Jukka Kallijärvi
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-16 (2017)
Abstract Mitochondrial disorders are among the most prevalent inborn errors of metabolism but largely lack treatments and have poor outcomes. High-fat, low-carbohydrate ketogenic diets (KDs) have shown beneficial effects in mouse models of mitochondr
Externí odkaz:
https://doaj.org/article/78dd4d8abb004a4485544bb1aa809497