نتائج البحث - Gruber, Robert
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Ichthyosis Update: Towards a Function-Driven Model of Pathogenesis of the Disorders of Cornification and the Role of Corneocyte Proteins in These Disorders حسب Schmuth, Matthias, Gruber, Robert, Elias, Peter M., Williams, Mary L.
منشور في 2007نص -
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Keratinocyte‐derived IL‐1β induces PPARG downregulation and PPARD upregulation in human reconstructed epidermis following barrier impairment حسب Blunder, Stefan, Krimbacher, Thomas, Moosbrugger‐Martinz, Verena, Gruber, Robert, Schmuth, Matthias, Dubrac, Sandrine
منشور في 2021نص -
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Filaggrin null mutations are associated with altered circulating Tregs in atopic dermatitis حسب Moosbrugger‐Martinz, Verena, Gruber, Robert, Ladstätter, Katharina, Bellutti, Marion, Blunder, Stefan, Schmuth, Matthias, Dubrac, Sandrine
منشور في 2018نص -
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Epidermal Barrier Dysfunction in Non-Atopic HIV: Evidence for an “Inside-to-Outside” Pathogenesis حسب Gunathilake, Roshan, Schmuth, Matthias, Scharschmidt, Tiffany C., Gruber, Robert, Grabher, Daniela, Leslie, Kieron S., Maurer, Toby A., Mauro, Theodora M., Elias, Peter M.
منشور في 2009نص -
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Epidermal Overexpression of Xenobiotic Receptor PXR Impairs the Epidermal Barrier and Triggers Th2 Immune Response حسب Elentner, Andreas, Schmuth, Matthias, Yannoutsos, Nikolaos, Eichmann, Thomas O., Gruber, Robert, Radner, Franz P.W., Hermann, Martin, Del Frari, Barbara, Dubrac, Sandrine
منشور في 2017نص -
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Induced pluripotent stem cell line from an atopic dermatitis patient heterozygous for c.2282del4 mutation in filaggrin: KCLi001-A حسب Devito, Liani, Donne, Matthew, Kolundzic, Nikola, Khurana, Preeti, Hobbs, Carl, Kaddour, Gabriel, Dubrac, Sandrine, Gruber, Robert, Schmuth, Matthias, Mauro, Thea, Ilic, Dusko
منشور في 2018نص -
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Alterations in Epidermal Eicosanoid Metabolism Contribute to Inflammation and Impaired Late Differentiation in FLG-Mutated Atopic Dermatitis حسب Blunder, Stefan, Rühl, Ralph, Moosbrugger-Martinz, Verena, Krimmel, Christine, Geisler, Anita, Zhu, Huiting, Crumrine, Debra, Elias, Peter M., Gruber, Robert, Schmuth, Matthias, Dubrac, Sandrine
منشور في 2016نص -
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Peroxisomal Fatty Acid Oxidation and Glycolysis Are Triggered in Mouse Models of Lesional Atopic Dermatitis حسب Pavel, Petra, Leman, Géraldine, Hermann, Martin, Ploner, Christian, Eichmann, Thomas O., Minzaghi, Deborah, Radner, Franz P.W., Del Frari, Barbara, Gruber, Robert, Dubrac, Sandrine
منشور في 2021نص -
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Tight Junction barriers in human hair follicles – role of claudin-1 حسب Zorn-Kruppa, Michaela, Vidal-y-Sy, Sabine, Houdek, Pia, Wladykowski, Ewa, Grzybowski, Stephan, Gruber, Robert, Gorzelanny, Christian, Harcup, Jason, Schneider, Stefan W., Majumdar, Amitabha, Brandner, Johanna M.
منشور في 2018نص -
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Unbound Corneocyte Lipid Envelopes in 12R-Lipoxygenase Deficiency Support a Specific Role in Lipid-Protein Cross-Linking حسب Meyer, Jason M., Crumrine, Debra, Schneider, Holm, Dick, Angela, Schmuth, Matthias, Gruber, Robert, Radner, Franz P.W., Grond, Susanne, Wakefield, Joan S., Mauro, Theodora M., Elias, Peter M.
منشور في 2021نص -
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Loss of Dermatan-4-Sulfotransferase 1 Function Results in Adducted Thumb-Clubfoot Syndrome حسب Dündar, Munis, Müller, Thomas, Zhang, Qi, Pan, Jing, Steinmann, Beat, Vodopiutz, Julia, Gruber, Robert, Sonoda, Tohru, Krabichler, Birgit, Utermann, Gerd, Baenziger, Jacques U., Zhang, Lijuan, Janecke, Andreas R.
منشور في 2009نص -
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Cellular Basis of Secondary Infections and Impaired Desquamation in Certain Inherited Ichthyoses حسب Chan, Aegean, Godoy-Gijon, Elena, Nuno-Gonzalez, Almudena, Crumrine, Debra, Hupe, Melanie, Choi, Eung-Ho, Gruber, Robert, Williams, Mary L., Choate, Keith, Fleckman, Philip H., Elias, Peter M.
منشور في 2015نص -
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Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency حسب Gruber, Robert, Sugarman, Jeffrey L., Crumrine, Debra, Hupe, Melanie, Mauro, Theodora M., Mauldin, Elizabeth A., Thyssen, Jacob P., Brandner, Johanna M., Hennies, Hans-Christian, Schmuth, Matthias, Elias, Peter M.
منشور في 2015نص -
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hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers حسب Lima Cunha, Dulce, Oram, Amanda, Gruber, Robert, Plank, Roswitha, Lingenhel, Arno, Gupta, Manoj K., Altmüller, Janine, Nürnberg, Peter, Schmuth, Matthias, Zschocke, Johannes, Šarić, Tomo, Eckl, Katja M., Hennies, Hans C.
منشور في 2021نص -
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Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V حسب Eckl, Katja M., Gruber, Robert, Brennan, Louise, Marriott, Andrew, Plank, Roswitha, Moosbrugger-Martinz, Verena, Blunder, Stefan, Schossig, Anna, Altmüller, Janine, Thiele, Holger, Nürnberg, Peter, Zschocke, Johannes, Hennies, Hans Christian, Schmuth, Matthias
منشور في 2021نص -
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Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and Pakistan حسب Lima Cunha, Dulce, Alakloby, Omar Mohammed, Gruber, Robert, Kakar, Naseebullah, Ahmad, Jamil, Alawbathani, Salem, Plank, Roswitha, Eckl, Katja, Krabichler, Birgit, Altmüller, Janine, Nürnberg, Peter, Zschocke, Johannes, Borck, Guntram, Schmuth, Matthias, Alabdulkareem, Adnan S., Abdulaziz Alnutaifi, Kholood, Hennies, Hans Christian
منشور في 2019نص