1 - 25 of 46 results for author:"Hohl D." in Literature citations
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| Nrf2 links epidermal barrier function with antioxidant defense. Schafer M., Farwanah H., Willrodt A.H., Huebner A.J., Sandhoff K., Roop D., Hohl D., Bloch W., Werner S. EMBO Mol Med 4:364-379(2012) · Mapped (2) |
| Homeodomain-only protein HOP is a novel modulator of late differentiation in keratinocytes. Obarzanek-Fojt M., Favre B., Kypriotou M., Ryser S., Huber M., Hohl D. Eur. J. Cell Biol. 90:279-290(2011) · Mapped (3) |
| The TRAF-interacting protein (TRIP) is a regulator of keratinocyte proliferation. Almeida S., Ryser S., Obarzanek-Fojt M., Hohl D., Huber M. J. Invest. Dermatol. 131:349-357(2011) · Mapped (6) |
| Atopic dermatitis-like disease and associated lethal myeloproliferative disorder arise from loss of Notch signaling in the murine skin. Dumortier A., Durham A.D., Di Piazza M., Vauclair S., Koch U., Ferrand G., Ferrero I., Demehri S., Song L.L., Farr A.G. et al. PLoS ONE 5:e9258-e9258(2010) · Mapped (22) |
| Loss of serum response factor in keratinocytes results in hyperproliferative skin disease in mice. Koegel H., von Tobel L., Schafer M., Alberti S., Kremmer E., Mauch C., Hohl D., Wang X.J., Beer H.D., Bloch W. et al. J. Clin. Invest. 119:899-910(2009) · Mapped (1) |
| Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis. Wen Y., Liu Y., Xu Y., Zhao Y., Hua R., Wang K., Sun M., Li Y., Yang S., Zhang X.J. et al. Nat. Genet. 41:228-233(2009) · UniProtKB (1) |
| Cutaneous cancer stem cell maintenance is dependent on beta-catenin signalling. Malanchi I., Peinado H., Kassen D., Hussenet T., Metzger D., Chambon P., Huber M., Hohl D., Cano A., Birchmeier W. et al. Nature 452:650-653(2008) · Mapped (24) |
| Human epidermal Langerhans cells express the tight junction protein claudin-1 and are present in human genetic claudin-1 deficiency (NISCH syndrome). Zimmerli S.C., Kerl K., Hadj-Rabia S., Hohl D., Hauser C. Exp. Dermatol. 17:20-23(2008) · Mapped (4) |
| Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis. Thomas A.C., Sinclair C., Mahmud N., Cullup T., Mellerio J.E., Harper J., Dale B.A., Turc-Carel C., Hohl D., McGrath J.A. et al. Br. J. Dermatol. 158:611-613(2008) · Mapped (2) |
| Five new CYLD mutations in skin appendage tumors and evidence that aspartic acid 681 in CYLD is essential for deubiquitinase activity. Almeida S., Maillard C., Itin P., Hohl D., Huber M. J. Invest. Dermatol. 128:587-593(2008) · Mapped (5) |
| The inflammasome mediates UVB-induced activation and secretion of interleukin-1beta by keratinocytes. Feldmeyer L., Keller M., Niklaus G., Hohl D., Werner S., Beer H.D. Curr. Biol. 17:1140-1145(2007) · Mapped (4) |
| Notch1 is a p53 target gene involved in human keratinocyte tumor suppression through negative regulation of ROCK1/2 and MRCKalpha kinases. Lefort K., Mandinova A., Ostano P., Kolev V., Calpini V., Kolfschoten I., Devgan V., Lieb J., Raffoul W., Hohl D. et al. Genes Dev. 21:562-577(2007) · Mapped (16) |
| SLURP1 is a late marker of epidermal differentiation and is absent in Mal de Meleda. Favre B., Plantard L., Aeschbach L., Brakch N., Christen-Zaech S., de Viragh P.A., Sergeant A., Huber M., Hohl D. J. Invest. Dermatol. 127:301-308(2007) · UniProtKB (1) |
| Nrf transcription factors in keratinocytes are essential for skin tumor prevention but not for wound healing. auf dem Keller U., Huber M., Beyer T.A., Kumin A., Siemes C., Braun S., Bugnon P., Mitropoulos V., Johnson D.A., Johnson J.A. et al. Mol. Cell. Biol. 26:3773-3784(2006) · Mapped (2) |
| Confirmation of the origin of NISCH syndrome. Feldmeyer L., Huber M., Fellmann F., Beckmann J.S., Frenk E., Hohl D. Hum. Mutat. 27:408-410(2006) · UniProtKB (1) |
| A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis. Muller F.B., Huber M., Kinaciyan T., Hausser I., Schaffrath C., Krieg T., Hohl D., Korge B.P., Arin M.J. Hum. Mol. Genet. 15:1133-1141(2006) · Mapped (1) |
| Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in ABCC6. Miksch S., Lumsden A., Guenther U.P., Foernzler D., Christen-Zach S., Daugherty C., Ramesar R.K., Lebwohl M., Hohl D., Neldner K.H. et al. |
| Isolation and characterization of human repetin, a member of the fused gene family of the epidermal differentiation complex. Huber M., Siegenthaler G., Mirancea N., Marenholz I., Nizetic D., Breitkreutz D., Mischke D., Hohl D. J. Invest. Dermatol. 124:998-1007(2005) · UniProtKB (1) |
| Cornulin, a new member of the 'fused gene' family, is expressed during epidermal differentiation. Contzler R., Favre B., Huber M., Hohl D. J. Invest. Dermatol. 124:990-997(2005) · UniProtKB (1) · Mapped (1) |
| Epidermal detachment, desmosomal dissociation, and destabilization of corneodesmosin in Spink5-/- mice. Yang T., Liang D., Koch P.J., Hohl D., Kheradmand F., Overbeek P.A. Genes Dev. 18:2354-2358(2004) · Mapped (19) |
| Infection with Human Papillomavirus alters expression of the small proline rich proteins 2 and 3. Lehr E., Hohl D., Huber M., Brown D. J. Med. Virol. 72:478-483(2004) · Mapped (2) |
| The tumor suppressor CYLD interacts with TRIP and regulates negatively nuclear factor kappaB activation by tumor necrosis factor. Regamey A., Hohl D., Liu J.W., Roger T., Kogerman P., Toftgaard R., Huber M. J. Exp. Med. 198:1959-1964(2003) · UniProtKB (2) · Mapped (9) |
| Molecular interaction of connexin 30.3 and connexin 31 suggests a dominant-negative mechanism associated with erythrokeratodermia variabilis. Plantard L., Huber M., Macari F., Meda P., Hohl D. Hum. Mol. Genet. 12:3287-3294(2003) · Mapped (2) |
| Identification of SLURP-1 as an epidermal neuromodulator explains the clinical phenotype of Mal de Meleda. Chimienti F., Hogg R.C., Plantard L., Lehmann C., Brakch N., Fischer J., Huber M., Bertrand D., Hohl D. Hum. Mol. Genet. 12:3017-3024(2003) · Mapped (1) |
| LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome. Bitoun E., Micheloni A., Lamant L., Bonnart C., Tartaglia-Polcini A., Cobbold C., Al Saati T., Mariotti F., Mazereeuw-Hautier J., Boralevi F. et al. Hum. Mol. Genet. 12:2417-2430(2003) · Mapped (3) |