Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Kaisa, Kettunen"'
Autor:
Virpi Glumoff, Janna Saarela, Timo Hautala, Nina Maria Hautala, Zhi Chen, Katri Pylkäs, Mira Siiskonen, Maija Joensuu, Teija Paakkola, Kaisa Kettunen
Publikováno v:
BMJ Open Ophthalmology, Vol 9, Iss 1 (2024)
Objective Ocular toxoplasmosis (OT) can cause posterior uveitis; causes of recurrent OT are not well understood. We explored clinical, immunological and genetic properties associated with recurrent OT.Methods and analysis A recurrent OT patient popul
Externí odkaz:
https://doaj.org/article/14f4447a47e44969a3f2220e3d780039
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 11, Pp n/a-n/a (2022)
Abstract Background Deletions covering the entire or partial JARID2 gene as well as pathogenic single nucleotide variants leading to haploinsufficiency of JARID2 have recently been shown to cause a clinically distinct neurodevelopmental syndrome. Her
Externí odkaz:
https://doaj.org/article/c9e540bba66b43cbaaff51cc7bce2fdf
Autor:
Minna Honkila, Riitta Niinimäki, Mervi Taskinen, Outi Kuismin, Kaisa Kettunen, Janna Saarela, Sami Turunen, Marjo Renko, Terhi Tapiainen
Publikováno v:
BMC Infectious Diseases, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Symptomatic primary Epstein-Barr virus infection is a usually self-limiting illness in adolescents. We present a case of an adolescent who had been receiving azathioprine for inflammatory bowel disease for four years and developed
Externí odkaz:
https://doaj.org/article/66d0326654164f04ae48b1d92236d439
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:
Teija Raivisto, AnnaMaria Heikkinen, Leena Kovanen, Hellevi Ruokonen, Kaisa Kettunen, Taina Tervahartiala, Jari Haukka, Timo Sorsa
Publikováno v:
International Journal of Dentistry, Vol 2018 (2018)
Background. Dental caries is the most common infection in the world and is influenced by genetic and environmental factors. Environmental factors are largely known, but the role of genetic factors is quite unknown. The aim was to investigate the gene
Externí odkaz:
https://doaj.org/article/bdf054e1b5ba4f43b2fd7aadca4252b3
Autor:
Anna Maria Heikkinen, Elmira Pakbaznejad Esmaeili, Leena Kovanen, Hellevi Ruokonen, Kaisa Kettunen, Jari Haukka, Taina Tervahartiala, Timo Sorsa
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 7, Pp ZC25-ZC28 (2017)
Introduction: Periodontitis is a multifactorial infectious disease of the supporting tissues of teeth in which bacterial, genetic and lifestyle factors such as smoking have an important role. Aim: The aim was to examine if Bleeding On Probing (BOP
Externí odkaz:
https://doaj.org/article/580fa3eccdc649bca2f3b707f2132765
Autor:
Miikka Ermes, Antti Kallonen, Teemu Perheentupa, R Sallinen, Heidi Similä, Ilkka Jokinen, Maritta Perälä-Heape, Cecilia Hellström, Samuli Ripatti, Myles Byrne, Tojo James, Hans Stenlund, Maja Neiman, Olli Kallioniemi, Peter Nilsson, Mikko Lindholm, Kaisa Kettunen, Harri Honko, Anu Karhu, Fredrik Boulund, Francesco Marabita, Thomas Moritz, Pyry Helkkula, Heidi Virtanen, Elisabeth Widen, Lars Engstrand, Hannele Laivuori, Robert Mills, Timo Miettinen
Publikováno v:
Marabita, F, James, T, Karhu, A, Virtanen, H, Kettunen, K, Stenlund, H, Boulund, F, Hellström, C, Neiman, M, Mills, R, Perheentupa, T, Laivuori, H, Helkkula, P, Byrne, M, Jokinen, I, Honko, H, Kallonen, A, Ermes, M, Similä, H, Lindholm, M, Widén, E, Ripatti, S, Perälä-Heape, M, Engstrand, L, Nilsson, P, Moritz, T, Miettinen, T, Sallinen, R & Kallioniemi, O 2022, ' Multiomics and digital monitoring during lifestyle changes reveal independent dimensions of human biology and health ', Cell Systems, vol. 13, no. 3, pp. 241-255.e7 . https://doi.org/10.1016/j.cels.2021.11.001
We explored opportunities for personalized and predictive health care by collecting serial clinical measurements, health surveys, genomics, proteomics, autoantibodies, metabolomics, and gut microbiome data from 96 individuals who participated in a da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8339b0021d90821349854037577a5ab4
https://curis.ku.dk/portal/da/publications/multiomics-and-digital-monitoring-during-lifestyle-changes-reveal-independent-dimensions-of-human-biology-and-health(e8f86864-ef9c-4ebb-ae6f-7297e303735c).html
https://curis.ku.dk/portal/da/publications/multiomics-and-digital-monitoring-during-lifestyle-changes-reveal-independent-dimensions-of-human-biology-and-health(e8f86864-ef9c-4ebb-ae6f-7297e303735c).html
Autor:
Iivo, Hetemäki, Meri, Kaustio, Matias, Kinnunen, Nelli, Heikkilä, Salla, Keskitalo, Kirsten, Nowlan, Simo, Miettinen, Joona, Sarkkinen, Virpi, Glumoff, Noora, Andersson, Kaisa, Kettunen, Reetta, Vanhanen, Katariina, Nurmi, Kari K, Eklund, Johannes, Dunkel, Mikko I, Mäyränpää, Heinrich, Schlums, T Petteri, Arstila, Kai, Kisand, Yenan T, Bryceson, Pärt, Peterson, Ulla, Otava, Jaana, Syrjänen, Janna, Saarela, Markku, Varjosalo, Eliisa, Kekäläinen
Publikováno v:
Science immunology. 6(65)
The Ikaros family transcription factors regulate lymphocyte development. Loss-of-function variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::653382fc70b384af21c884f81f1d52d3
https://pubmed.ncbi.nlm.nih.gov/34826260
https://pubmed.ncbi.nlm.nih.gov/34826260
Autor:
Jaana Syrjänen, Heinrich Schlums, Yenan T. Bryceson, Iivo Hetemäki, Salla Keskitalo, Meri Kaustio, Noora Andersson, Nelli Heikkilä, Kari K. Eklund, Virpi Glumoff, Matias Kinnunen, Mikko I. Mäyränpää, Simo Miettinen, T. Petteri Arstila, Joona Sarkkinen, Kai Kisand, Johannes Dunkel, Reetta Vanhanen, Katariina Nurmi, Ulla Otava, Eliisa Kekäläinen, Kaisa Kettunen, Markku Varjosalo, Janna Saarela, Pärt Peterson
The IKAROS family transcription factors regulate lymphocyte development. Loss-of-function variants in IKZF1 cause primary immunodeficiency, but IKAROS family members IKZF2 and IKZF3 have not yet been associated with immunodeficiency yet. Here, we des
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de462bc93bc0f7f14249247ed95d486b
https://doi.org/10.1101/2021.08.25.21262015
https://doi.org/10.1101/2021.08.25.21262015
Autor:
V Karvonen, Pekka Ellonen, Katariina Hannula-Jouppi, Kaisa Kettunen, Outi Elomaa, Janna Saarela, H. Heikkilä, Elisabet Einarsdottir, Liisa Harjama, Juha Kere, Annamari Ranki, Sirpa Kivirikko
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADVReferences. 35(9)
Background Hereditary palmoplantar keratodermas (PPK) represent a heterogeneous group of rare skin disorders with epidermal hyperkeratosis of the palms and soles, with occasional additional manifestations in other tissues. Mutations in at least 69 ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af381b6f1be377e19fc929c311c69a51
https://pubmed.ncbi.nlm.nih.gov/33914963
https://pubmed.ncbi.nlm.nih.gov/33914963