Rezultati pretrage - Vahlquist, Anders

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Detaljiziraj rezultate
  1. 1
    Ichthyosis: A Road Model for Skin Research()

    Ichthyosis: A Road Model for Skin Research() od VAHLQUIST, Anders, TÖRMÄ, Hans

    Izdano 2020
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  2. 2
    Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment

    Inherited Nonsyndromic Ichthyoses: An Update on Pathophysiology, Diagnosis and Treatment od Vahlquist, Anders, Fischer, Judith, Törmä, Hans

    Izdano 2017
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  3. 3
    Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response?

    Patients with congenital ichthyosis and TGM1 mutations overexpress other ARCI genes in the skin: Part of a barrier repair response? od Zhang, Hanqian, Ericsson, Maja, Weström, Simone, Vahlquist, Anders, Virtanen, Marie, Törmä, Hans

    Izdano 2018
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  4. 4
    Filaggrin Genotype Determines Functional and Molecular Alterations in Skin of Patients with Atopic Dermatitis and Ichthyosis Vulgaris

    Filaggrin Genotype Determines Functional and Molecular Alterations in Skin of Patients with Atopic Dermatitis and Ichthyosis Vulgaris od Winge, Mårten C. G., Hoppe, Torborg, Berne, Berit, Vahlquist, Anders, Nordenskjöld, Magnus, Bradley, Maria, Törmä, Hans

    Izdano 2011
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  5. 5
    Mutations in the Fatty Acid Transport Protein 4 Gene Cause the Ichthyosis Prematurity Syndrome

    Mutations in the Fatty Acid Transport Protein 4 Gene Cause the Ichthyosis Prematurity Syndrome od Klar, Joakim, Schweiger, Martina, Zimmerman, Robert, Zechner, Rudolf, Li, Hao, Törmä, Hans, Vahlquist, Anders, Bouadjar, Bakar, Dahl, Niklas, Fischer, Judith

    Izdano 2009
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  6. 6
    Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26

    Revertant mosaicism repairs skin lesions in a patient with keratitis-ichthyosis-deafness syndrome by second-site mutations in connexin 26 od Gudmundsson, Sanna, Wilbe, Maria, Ekvall, Sara, Ameur, Adam, Cahill, Nicola, Alexandrov, Ludmil B., Virtanen, Marie, Hellström Pigg, Maritta, Vahlquist, Anders, Törmä, Hans, Bondeson, Marie-Louise

    Izdano 2017
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  7. 7
    A Single-Nucleotide Deletion in the POMP 5′ UTR Causes a Transcriptional Switch and Altered Epidermal Proteasome Distribution in KLICK Genodermatosis

    A Single-Nucleotide Deletion in the POMP 5′ UTR Causes a Transcriptional Switch and Altered Epidermal Proteasome Distribution in KLICK Genodermatosis od Dahlqvist, Johanna, Klar, Joakim, Tiwari, Neha, Schuster, Jens, Törmä, Hans, Badhai, Jitendra, Pujol, Ramon, van Steensel, Maurice A.M., Brinkhuizen, Tjinta, Gijezen, Lieke, Chaves, Antonio, Tadini, Gianluca, Vahlquist, Anders, Dahl, Niklas

    Izdano 2010
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  8. 8
    A Single-Nucleotide Deletion in the POMP 5′ UTR Causes a Transcriptional Switch and Altered Epidermal Proteasome Distribution in KLICK Genodermatosis

    A Single-Nucleotide Deletion in the POMP 5′ UTR Causes a Transcriptional Switch and Altered Epidermal Proteasome Distribution in KLICK Genodermatosis od Dahlqvist, Johanna, Klar, Joakim, Tiwari, Neha, Schuster, Jens, Törmä, Hans, Badhai, Jitendra, Pujol, Ramon, van Steensel, Maurice A.M., Brinkhuizen, Tjinta, Gijezen, Lieke, Chaves, Antonio, Tadini, Gianluca, Vahlquist, Anders, Dahl, Niklas

    Izdano 2010
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  9. 9
    Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients

    Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients od Hotz, Alrun, Kopp, Julia, Bourrat, Emmanuelle, Oji, Vinzenz, Komlosi, Katalin, Giehl, Kathrin, Bouadjar, Bakar, Bygum, Anette, Tantcheva-Poor, Iliana, Hellström Pigg, Maritta, Has, Cristina, Yang, Zhou, Irvine, Alan D., Betz, Regina C., Zambruno, Giovanna, Tadini, Gianluca, Süßmuth, Kira, Gruber, Robert, Schmuth, Matthias, Mazereeuw-Hautier, Juliette, Jonca, Natalie, Guez, Sophie, Brena, Michela, Hernandez-Martin, Angela, van den Akker, Peter, Bolling, Maria C., Hannula-Jouppi, Katariina, Zimmer, Andreas D., Alter, Svenja, Vahlquist, Anders, Fischer, Judith

    Izdano 2021
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