Pesquisa | BVS Doenças Infecciosas e Parasitárias

1.

Unbound Corneocyte Lipid Envelopes in 12R-Lipoxygenase Deficiency Support a Specific Role in Lipid-Protein Cross-Linking.

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.

Am J Pathol ; 191(5): 921-929, 2021 05.

Artigo em Inglês | MEDLINE | ID: mdl-33607042

2.

Revisiting the Roles of Filaggrin in Atopic Dermatitis.

Moosbrugger-Martinz, Verena; Leprince, Corinne; Méchin, Marie-Claire; Simon, Michel; Blunder, Stefan; Gruber, Robert; Dubrac, Sandrine.

Int J Mol Sci ; 23(10)2022 May 10.

Artigo em Inglês | MEDLINE | ID: mdl-35628125

3.

Keratinocyte-derived IL-1ß induces PPARG downregulation and PPARD upregulation in human reconstructed epidermis following barrier impairment.

Blunder, Stefan; Krimbacher, Thomas; Moosbrugger-Martinz, Verena; Gruber, Robert; Schmuth, Matthias; Dubrac, Sandrine.

Exp Dermatol ; 30(9): 1298-1308, 2021 09.

Artigo em Inglês | MEDLINE | ID: mdl-33683743

4.

hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers.

Lima Cunha, Dulce; Oram, Amanda; Gruber, Robert; Plank, Roswitha; Lingenhel, Arno; Gupta, Manoj K; Altmüller, Janine; Nürnberg, Peter; Schmuth, Matthias; Zschocke, Johannes; Saric, Tomo; Eckl, Katja M; Hennies, Hans C.

Int J Mol Sci ; 22(4)2021 Feb 11.

Artigo em Inglês | MEDLINE | ID: mdl-33670118

5.

Aggregated neutrophil extracellular traps resolve inflammation by proteolysis of cytokines and chemokines and protection from antiproteases.

Hahn, Jonas; Schauer, Christine; Czegley, Christine; Kling, Lasse; Petru, Lenka; Schmid, Benjamin; Weidner, Daniela; Reinwald, Christiane; Biermann, Mona H C; Blunder, Stefan; Ernst, Jürgen; Lesner, Adam; Bäuerle, Tobias; Palmisano, Ralf; Christiansen, Silke; Herrmann, Martin; Bozec, Aline; Gruber, Robert; Schett, Georg; Hoffmann, Markus H.

FASEB J ; 33(1): 1401-1414, 2019 01.

Artigo em Inglês | MEDLINE | ID: mdl-30130433

6.

Spektrum der Ichthyosen in einer österreichischen Ichthyosekohorte von 2004-2007.

Seidl-Philipp, Magdalena; Schatz, Ulrich A; Gasslitter, Irina; Moosbrugger-Martinz, Verena; Blunder, Stefan; Schossig, Anna S; Zschocke, Johannes; Schmuth, Matthias; Gruber, Robert.

J Dtsch Dermatol Ges ; 18(1): 17-26, 2020 Jan.

Artigo em Alemão | MEDLINE | ID: mdl-31985158

7.

Spectrum of ichthyoses in an Austrian ichthyosis cohort from 2004 to 2017.

Seidl-Philipp, Magdalena; Schatz, Ulrich A; Gasslitter, Irina; Moosbrugger-Martinz, Verena; Blunder, Stefan; Schossig, Anna S; Zschocke, Johannes; Schmuth, Matthias; Gruber, Robert.

J Dtsch Dermatol Ges ; 18(1): 17-25, 2020 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-31642606

8.

Filaggrin null mutations are associated with altered circulating Tregs in atopic dermatitis.

Moosbrugger-Martinz, Verena; Gruber, Robert; Ladstätter, Katharina; Bellutti, Marion; Blunder, Stefan; Schmuth, Matthias; Dubrac, Sandrine.

J Cell Mol Med ; 23(2): 1288-1299, 2019 02.

Artigo em Inglês | MEDLINE | ID: mdl-30515983

9.

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement.

Kapferer-Seebacher, Ines; Pepin, Melanie; Werner, Roland; Aitman, Timothy J; Nordgren, Ann; Stoiber, Heribert; Thielens, Nicole; Gaboriaud, Christine; Amberger, Albert; Schossig, Anna; Gruber, Robert; Giunta, Cecilia; Bamshad, Michael; Björck, Erik; Chen, Christina; Chitayat, David; Dorschner, Michael; Schmitt-Egenolf, Marcus; Hale, Christopher J; Hanna, David; Hennies, Hans Christian; Heiss-Kisielewsky, Irene; Lindstrand, Anna; Lundberg, Pernilla; Mitchell, Anna L; Nickerson, Deborah A; Reinstein, Eyal; Rohrbach, Marianne; Romani, Nikolaus; Schmuth, Matthias; Silver, Rachel; Taylan, Fulya; Vandersteen, Anthony; Vandrovcova, Jana; Weerakkody, Ruwan; Yang, Margaret; Pope, F Michael; Byers, Peter H; Zschocke, Johannes.

Am J Hum Genet ; 99(5): 1005-1014, 2016 Nov 03.

Artigo em Inglês | MEDLINE | ID: mdl-27745832

10.

Ustekinumab treatment in severe atopic dermatitis: Down-regulation of T-helper 2/22 expression.

Weiss, Doris; Schaschinger, Michaela; Ristl, Robin; Gruber, Robert; Kopp, Tamara; Stingl, Georg; Bangert, Christine.

J Am Acad Dermatol ; 76(1): 91-97.e3, 2017 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-27745907

11.

Coincidence of Bullous Pemphigoid and Pityriasis Rubra Pilaris.

Gasslitter, Irina; Löffler-Ragg, Judith; Schmidt, Enno; Schmuth, Matthias; Gruber, Robert.

Acta Derm Venereol ; 102: adv00674, 2022 Mar 22.

Artigo em Inglês | MEDLINE | ID: mdl-35170740

12.

Journal-Club.

Gruber, Robert W.

J Dtsch Dermatol Ges ; 20(2): 246, 2022 02.

Artigo em Alemão | MEDLINE | ID: mdl-35146887

13.

Präzisionsmedizinischer Ansatz bei einem seltenen Fall von autosomal rezessiver kongenitaler Ichthyose.

Ettinger, Monika; Burner, Teresa; Lackner, Angelika; Schoeftner, Leonie C; Holzgruber, Julia; Gruber, Robert; Guenova, Emmanuella; Schuetz-Bergmayr, Martina; Fischer, Tobias; Gratz, Iris K; Kimeswenger, Susanne; Hoetzenecker, Wolfram.

J Dtsch Dermatol Ges ; 20(12): 1651-1654, 2022 12.

Artigo em Inglês | MEDLINE | ID: mdl-36508377

14.

Precision medicine approach in a rare case of autosomal recessive congenital ichthyosis.

Ettinger, Monika; Burner, Teresa; Lackner, Angelika; Schoeftner, Leonie C; Holzgruber, Julia; Gruber, Robert; Guenova, Emmanuella; Schuetz-Bergmayr, Martina; Fischer, Tobias; Gratz, Iris K; Kimeswenger, Susanne; Hoetzenecker, Wolfram.

J Dtsch Dermatol Ges ; 20(12): 1651-1653, 2022 12.

Artigo em Inglês | MEDLINE | ID: mdl-36442141

15.

Diverse regulation of claudin-1 and claudin-4 in atopic dermatitis.

Gruber, Robert; Börnchen, Christian; Rose, Katharina; Daubmann, Anne; Volksdorf, Thomas; Wladykowski, Ewa; Vidal-Y-Sy, Sabine; Peters, Eva M; Danso, Mogbekeloluwa; Bouwstra, Joke A; Hennies, Hans C; Moll, Ingrid; Schmuth, Matthias; Brandner, Johanna M.

Am J Pathol ; 185(10): 2777-89, 2015 Oct.

Artigo em Inglês | MEDLINE | ID: mdl-26319240

16.

Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiency.

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.

Am J Pathol ; 185(4): 1012-21, 2015 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-25660180

17.

Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin.

McAleer, Maeve A; Pohler, Elizabeth; Smith, Frances J D; Wilson, Neil J; Cole, Christian; MacGowan, Stuart; Koetsier, Jennifer L; Godsel, Lisa M; Harmon, Robert M; Gruber, Robert; Crumrine, Debra; Elias, Peter M; McDermott, Michael; Butler, Karina; Broderick, Annemarie; Sarig, Ofer; Sprecher, Eli; Green, Kathleen J; McLean, W H Irwin; Irvine, Alan D.

J Allergy Clin Immunol ; 136(5): 1268-76, 2015 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-26073755

18.

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.

Sandilands, Aileen; Terron-Kwiatkowski, Ana; Hull, Peter R; O'Regan, Gráinne M; Clayton, Timothy H; Watson, Rosemarie M; Carrick, Thomas; Evans, Alan T; Liao, Haihui; Zhao, Yiwei; Campbell, Linda E; Schmuth, Matthias; Gruber, Robert; Janecke, Andreas R; Elias, Peter M; van Steensel, Maurice A M; Nagtzaam, Ivo; van Geel, Michel; Steijlen, Peter M; Munro, Colin S; Bradley, Daniel G; Palmer, Colin N A; Smith, Frances J D; McLean, W H Irwin; Irvine, Alan D.

Nat Genet ; 39(5): 650-4, 2007 May.

Artigo em Inglês | MEDLINE | ID: mdl-17417636

19.

Journal-Club.

Gruber, Robert W.

J Dtsch Dermatol Ges ; 19(8): 1250, 2021 08.

Artigo em Alemão | MEDLINE | ID: mdl-34390154

20.

Formation and functions of the corneocyte lipid envelope (CLE).

Elias, Peter M; Gruber, Robert; Crumrine, Debra; Menon, Gopinathan; Williams, Mary L; Wakefield, Joan S; Holleran, Walter M; Uchida, Yoshikazu.

Biochim Biophys Acta ; 1841(3): 314-8, 2014 Mar.

Artigo em Inglês | MEDLINE | ID: mdl-24076475

BVS Doenças Infecciosas e Parasitárias

Informação e Conhecimento para a Saúde

Configurar filtros

Sua seleção (0)

Formato de exportação:

Exportar:

Unbound Corneocyte Lipid Envelopes in 12R-Lipoxygenase Deficiency Support a Specific Role in Lipid-Protein Cross-Linking.

Revisiting the Roles of Filaggrin in Atopic Dermatitis.

Keratinocyte-derived IL-1ß induces PPARG downregulation and PPARD upregulation in human reconstructed epidermis following barrier impairment.

hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers.

Aggregated neutrophil extracellular traps resolve inflammation by proteolysis of cytokines and chemokines and protection from antiproteases.

Spektrum der Ichthyosen in einer österreichischen Ichthyosekohorte von 2004-2007.

Spectrum of ichthyoses in an Austrian ichthyosis cohort from 2004 to 2017.

Filaggrin null mutations are associated with altered circulating Tregs in atopic dermatitis.

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement.

Ustekinumab treatment in severe atopic dermatitis: Down-regulation of T-helper 2/22 expression.

Coincidence of Bullous Pemphigoid and Pityriasis Rubra Pilaris.

Journal-Club.

Präzisionsmedizinischer Ansatz bei einem seltenen Fall von autosomal rezessiver kongenitaler Ichthyose.

Precision medicine approach in a rare case of autosomal recessive congenital ichthyosis.

Diverse regulation of claudin-1 and claudin-4 in atopic dermatitis.

Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiency.

Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin.

Comprehensive analysis of the gene encoding filaggrin uncovers prevalent and rare mutations in ichthyosis vulgaris and atopic eczema.

Journal-Club.

Formation and functions of the corneocyte lipid envelope (CLE).