Zobrazeno 1 - 10
of 43
pro vyhledávání: '"H. Annika"'
Autor:
Mari H. Tervaniemi, Shintaro Katayama, Tiina Skoog, H. Annika Siitonen, Jyrki Vuola, Kristo Nuutila, Kristiina Tammimies, Sari Suomela, Esko Kankuri, Juha Kere, Outi Elomaa
Publikováno v:
BMC Genomics, Vol 19, Iss 1, Pp 1-15 (2018)
Abstract Background CCHCR1 (Coiled-Coil α-Helical Rod protein 1) is a putative psoriasis candidate gene with the risk alleles CCHCR1*WWCC and *Iso3, the latter inhibiting the translation of isoform 1. CCHCR1 was recently shown to be a centrosomal pr
Externí odkaz:
https://doaj.org/article/4738f60bbc634fd9bf49693a449cf2e9
Autor:
Mari H Tervaniemi, H Annika Siitonen, Cilla Söderhäll, Gurinder Minhas, Jyrki Vuola, Inkeri Tiala, Raija Sormunen, Lena Samuelsson, Sari Suomela, Juha Kere, Outi Elomaa
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e49920 (2012)
CCHCR1 (Coiled-Coil α-Helical Rod protein 1), within the major psoriasis susceptibility locus PSORS1, is a plausible candidate gene with the psoriasis associated risk allele CCHCR1*WWCC. Although its expression pattern in psoriatic skin differs from
Externí odkaz:
https://doaj.org/article/e766049596e5457c8f30b1ee4cca5b82
Autor:
Arun Y. Patil, PK Pavan, Basvaraja B. Kotturshettar, Anirudh Kohli, Prasad B. Sarwad, B. Karthik, H. Annika, P. A. Lohit
Publikováno v:
Journal of Physics: Conference Series. 1706:012185
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20687eb5182957d6b8be053138b6fc00
https://doi.org/10.1088/1742-6596/1706/1/012185
https://doi.org/10.1088/1742-6596/1706/1/012185
Autor:
Kristiina Tammimies, Esko Kankuri, Mari H. Tervaniemi, Juha Kere, Kristo Nuutila, Shintaro Katayama, H. Annika Siitonen, Jyrki Vuola, Outi Elomaa, Tiina Skoog, Sari Suomela
Publikováno v:
BMC Genomics
BMC Genomics, Vol 19, Iss 1, Pp 1-15 (2018)
BMC Genomics, Vol 19, Iss 1, Pp 1-15 (2018)
Background CCHCR1 (Coiled-Coil α-Helical Rod protein 1) is a putative psoriasis candidate gene with the risk alleles CCHCR1*WWCC and *Iso3, the latter inhibiting the translation of isoform 1. CCHCR1 was recently shown to be a centrosomal protein, as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f59b675585b5ce6c2a1c5bf8312af71
http://hdl.handle.net/10138/236584
http://hdl.handle.net/10138/236584
Autor:
Tervaniemi, Mari H.1,2,3 (AUTHOR), Siitonen, H. Annika1,2,3 (AUTHOR), Söderhäll, Cilla4 (AUTHOR), Minhas, Gurinder1,2,3 (AUTHOR), Vuola, Jyrki5 (AUTHOR), Tiala, Inkeri1,2,3 (AUTHOR), Sormunen, Raija6 (AUTHOR), Samuelsson, Lena7 (AUTHOR), Suomela, Sari8 (AUTHOR), Kere, Juha1,2,3,4,9 (AUTHOR) juha.kere@ki.se, Elomaa, Outi1,2,3 (AUTHOR)
Publikováno v:
PLoS ONE. Nov2012, Vol. 7 Issue 11, Special section p1-13. 13p.
Autor:
Siitonen, H. Annika1, Sotkasiira, Jenni1, Biervliet, Martine2, Benmansour, Abdelmadjid3, Capri, Yline4, Cormier-Daire, Valerie5, Crandall, Barbara6, Hannula-Jouppi, Katariina7, Hennekam, Raoul8,9, Herzog, Denise10, Keymolen, Kathelijn11, Lipsanen-Nyman, Marita12, Miny, Peter13, Plon, Sharon E.14, Riedl, Stefan15, Sarkar, Ajoy16, Vargas, Fernando R.17, Verloes, Alain18, Wang, Lisa L.19, Kääriäinen, Helena1,20
Publikováno v:
European Journal of Human Genetics. Feb2009, Vol. 17 Issue 2, p151-158. 8p. 2 Charts.
Autor:
Sznajer, Yves1 yves.sznajer@ulb.ac.be, Siitonen, H. Annika2, Roversi, Gaia3, Dangoisse, Chantal4, Scaillon, Michèle5, Ziereisen, France6, Tenoutasse, Sylvie7, Kestilä, Marjo2, Larizza, Lidia3, Scaillon, Michèle (AUTHOR), Kestilä, Marjo (AUTHOR)
Publikováno v:
European Journal of Pediatrics. Feb2008, Vol. 167 Issue 2, p175-181. 7p. 1 Color Photograph, 1 Black and White Photograph, 1 Chart, 1 Graph.
Akademický článek
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NOD-like receptor signaling and inflammasome-related pathways are highlighted in psoriatic epidermis
Autor:
H. Annika Siitonen, Raija Sormunen, Tiina Skoog, Esko Kankuri, Kristo Nuutila, Juha Kere, Sari Suomela, Sten Linnarsson, Mari H. Tervaniemi, Shintaro Katayama, Jyrki Vuola, Outi Elomaa, Anna Johnsson
Publikováno v:
Scientific Reports
Psoriatic skin differs distinctly from normal skin by its thickened epidermis. Most gene expression comparisons utilize full-thickness biopsies, with substantial amount of dermis. We assayed the transcriptomes of normal, lesional and non-lesional pso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea9f1d25cdc2882138adc2084df206d8
http://hdl.handle.net/10138/161087
http://hdl.handle.net/10138/161087
Autor:
Valérie Cormier-Daire, Sharon E. Plon, Kathelijn Keymolen, Katariina Hannula-Jouppi, Jenni Sotkasiira, Ajoy Sarkar, Denise Herzog, Martine Biervliet, Abdelmadjid Benmansour, Alain Verloes, Raoul C.M. Hennekam, Fernando Regla Vargas, Peter Miny, Marita Lipsanen-Nyman, Lisa L. Wang, Marjo Kestilä, Yline Capri, Helena Kääriäinen, H. Annika Siitonen, Stefan Riedl, Barbara F. Crandall
Publikováno v:
European journal of human genetics
European journal of human genetics, 17(2), 151-158. Nature Publishing Group
European journal of human genetics, 17(2), 151-158. Nature Publishing Group
Mutations in the RECQL4 gene can lead to three clinical phenotypes with overlapping features. All these syndromes, Rothmund-Thomson (RTS), RAPADILINO and Baller-Gerold (BGS), are characterized by growth retardation and radial defects, but RAPADILINO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b2446c70cdb054924338195d7195b6d
https://doi.org/10.1038/ejhg.2008.154
https://doi.org/10.1038/ejhg.2008.154