Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Marie Virtanen"'
Autor:
Daniel Eriksson, MD, PhD, David Gyll, MD, Marie Virtanen, MD, Niklas Dahl, MD, PhD, Joakim Klar, PhD, Eva-Lena Stattin, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 31, Iss , Pp 133-136 (2023)
Externí odkaz:
https://doaj.org/article/0a02f400cc9e4b329a3103676566ad64
Autor:
Mikael Alsterholm, Axel Svedbom, Chris D. Anderson, Lena Holm Sommar, Lina U. Ivert, Anna Josefson, Laura von Kobyletzki, Magnus Lindberg, Lena Lundeberg, Maria Lundqvist, Elisabet Nylander, MariHelen Sandström Falk, Alexander Shayesteh, Gunnthorunn Sigurdardottir, Andreas Sonesson, Åke Svensson, Marie Virtanen, Sophie Vrang, Carl-Fredrik Wahlgren, Maria Bradley, Emma K. Johansson
Publikováno v:
Acta Dermato-Venereologica, Vol 103 (2023)
SwedAD, a Swedish nationwide registry for patients with atopic dermatitis receiving systemic pharmacotherapy, was launched on 1 September 2019. We describe here the establishment of a user-friendly registry to the benefit of patients with atopic derm
Externí odkaz:
https://doaj.org/article/3cf0af5bf0dd44eba4f3bf4a73a39f27
Publikováno v:
Differentiation; research in biological diversity. 119
A proper skin barrier function requires constant formation of stratum corneum, i.e. the outermost layer of epidermis composed of terminally differentiated keratinocytes. The complex process of converting proliferative basal keratinocytes into corneoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::245c343b4dbbae6121d04f214dfe7521
https://pubmed.ncbi.nlm.nih.gov/34029921
https://pubmed.ncbi.nlm.nih.gov/34029921
Autor:
Anders Vahlquist, Carolina Wählby, Marie Virtanen, Simone Weström, Maja Ericsson, Hans Törmä, Hanqian Zhang
Publikováno v:
Experimental Dermatology. 27:196-199
Immunofluorescence (IF) and in situ proximity ligation assay (isPLA) are techniques that are used for in situ protein expression and colocalisation analysis, respectively. However, an efficient quantitative method to analyse both IF and isPLA stainin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caebbc9cb72a7206ce5c29a4cc70a3a3
https://doi.org/10.1111/exd.13457
https://doi.org/10.1111/exd.13457
Autor:
Marie Virtanen, Andreas Zimmer, Judith Fischer, Anders Vahlquist, Alrun Hotz, Flemming Brandrup, Maritta Hellström Pigg, Anette Bygum, Agneta Gånemo
Publikováno v:
Hellström Pigg, M, Bygum, A, Gånemo, A, Virtanen, M, Brandrup, F, Zimmer, A D, Hotz, A, Vahlquist, A & Fischer, J 2016, ' Spectrum of Autosomal Recessive Congenital Ichthyosis in Scandinavia : Clinical Characteristics and Novel and Recurrent Mutations in 132 Patients ', Acta Dermato-Venereologica, vol. 96, no. 7, pp. 932–937 . https://doi.org/10.2340/00015555-2418
Autosomal recessive congenital ichthyosis (ARCI) represents a heterogeneous group of rare disorders of cornification with 3 major subtypes: harlequin ichthyosis (HI), lamellar ichthyosis (LI) and congenital ichthyosiform erythroderma (CIE). A 4th sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abd31d57059ea6062d729345541144a9
https://doi.org/10.2340/00015555-2418
https://doi.org/10.2340/00015555-2418
Autor:
Thomas Manke, Andreas Zimmer, Judith Fischer, Nina Schlipf, Anca Dragomir, S Fismen, Marie Virtanen, N Teigen, Bernd Rösler, Maxim Barenboim, Anders Vahlquist
Publikováno v:
British Journal of Dermatology. 174:444-448
Whole-exome sequencing identifies novel autosomal recessive DSG1 mutations associated with mild SAM syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::184342e2c57b4a9635bc31c7ddec310b
https://doi.org/10.1111/bjd.14079
https://doi.org/10.1111/bjd.14079
Autor:
Linshu, Zhao, Anders, Vahlquist, Marie, Virtanen, Lena, Wennerstrand, Lisbet K, Lind, Anita, Lundström, Maritta Hellström, Pigg
Publikováno v:
Acta dermato-venereologica. 95(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::152b9c1a215d8573f25e8b19c8eab5dd
https://pubmed.ncbi.nlm.nih.gov/26139149
https://pubmed.ncbi.nlm.nih.gov/26139149
Autor:
Anders Vahlquist, Harshad Navsaria, Hans Törmä, Therese Gester, Inger Pihl-Lundin, Jean Christopher Chamcheu, Marie Virtanen, Cedrique Eteti Mouyobo, Aristidis Moustakas
Publikováno v:
British Journal of Dermatology. 164:263-272
Background: Epidermolytic ichthyosis (EI) is a skin fragility disorder caused by mutations in genes encoding suprabasal keratins 1 and 10. While the aetiology of EI is known, model systems are need ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fef930a2e2c258e508ad0eb64b63ad6
https://doi.org/10.1111/j.1365-2133.2010.10092.x
https://doi.org/10.1111/j.1365-2133.2010.10092.x
Publikováno v:
Experimental Dermatology. 19:674-681
Disorders of keratinization are often treated with vitamin A derivatives (retinoids) which affect keratinocyte differentiation, including keratin (KRT) gene expression. In vivo, suprabasal keratinocytes normally express only keratin (K) 1, K2 and K10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6afa235d39b26b241c14a5d01f75d2c
https://doi.org/10.1111/j.1600-0625.2010.01079.x
https://doi.org/10.1111/j.1600-0625.2010.01079.x
Autor:
Anders Vahlquist, Hans Törmä, Jean Christopher Chamcheu, Marie Virtanen, Paul Edward Bowden, Harshad Navsaria
Publikováno v:
British Journal of Dermatology. 162:980-989
Background Epidermolysis bullosa simplex (EBS) is a mechanobullous skin fragility disease characterized by cytolysis of basal keratinocytes and intraepidermal blistering often caused by mutations in keratin genes (KRT5 or KRT14). No remedies exist fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7529af97f6fb29b5a55b68b61cd4773
https://doi.org/10.1111/j.1365-2133.2009.09615.x
https://doi.org/10.1111/j.1365-2133.2009.09615.x