Homeostasis of the sebaceous gland and mechanisms of acne pathogenesis von Clayton, R.W., Göbel, K., Niessen, C.M., Paus, R., Steensel, M.A.M., Lim, X.

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The emerging role of GATA transcription factors in development and disease von Lentjes, Marjolein HFM, Niessen, Hanneke EC, Akiyama, Yoshimitsu, de Bruïne, Adriaan P, Melotte, Veerle, van Engeland, Manon

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Germline hypermethylation of MLH1 and EPCAM deletions are a frequent cause of Lynch syndrome von Niessen, Renée C., Hofstra, Robert M. W., Westers, Helga, Ligtenberg, Marjolijn J. L., Kooi, Krista, Jager, Paul O. J., de Groote, Marloes L., Dijkhuizen, Trijnie, Olderode-Berends, Maran J. W., Hollema, Harry, Kleibeuker, Jan H., Sijmons, Rolf H.

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Analysis of Promoter CpG Island Hypermethylation in Cancer: Location, Location, Location von VAN VLODROP, Iris J. H, NIESSEN, Hanneke E. C, DERKS, Sarah, BALDEWIJNS, Marcella M. L. L, VAN CRIEKINGE, Wim, HERMAN, James G, VAN ENGELAND, Manon

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Obesity-induced metabolic stress accelerates hair loss von Niessen, C.

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Defining the Architecture of Skin Tumorigenesis von Niessen, C.

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Cellular Response to Mechanical Stretch in the Skin von Niessen, C.

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Resident SkinMicrobiota Trigger Wound Healing von Niessen, C.

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Impact of liver cirrhosis on liver enhancement at Gd-EOB-DTPA enhanced MRI at 3 Tesla von Verloh, N, Haimerl, M, Rennert, J, Müller-Wille, R, Nießen, C, Kirchner, G, Scherer, M.N, Schreyer, A.G, Stroszczynski, C, Fellner, C, Wiggermann, P

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Percutaneous Irreversible Electroporation: Long-term survival analysis of 71 patients with inoperable malignant hepatic tumors von Niessen, C., Thumann, S., Beyer, L., Pregler, B., Kramer, J., Lang, S., Teufel, A., Jung, E. M., Stroszczynski, C., Wiggermann, P.

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JunB acts as a gatekeeper of the immune-microbiota interface von Niessen, C.

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RIPK4 and IRF6 function in epidermal barrier formation von Niessen, C.

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MK3 modulation affects BMI1-dependent and independent cell cycle check-points von Prickaerts, Peggy, Niessen, Hanneke E C, Dahlmans, Vivian E H, Spaapen, Frank, Salvaing, Juliette, Vanhove, Jolien, Geijselaers, Claudia, Bartels, Stefanie J J, Partouns, Iris, Neumann, Dietbert, Speel, Ernst-Jan, Takihara, Yoshihiro, Wouters, Bradly G, Voncken, Jan Willem

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Recurrence and variability of germline EPCAM deletions in Lynch syndrome von Kuiper, Roland P., Vissers, Lisenka E.L.M., Venkatachalam, Ramprasath, Bodmer, Danielle, Hoenselaar, Eveline, Goossens, Monique, Haufe, Aline, Kamping, Eveline, Niessen, Renée C., Hogervorst, Frans B.L., Gille, Johan J.P., Redeker, Bert, Tops, Carli M.J., van Gijn, Marielle E., van den Ouweland, Ans M.W., Rahner, Nils, Steinke, Verena, Kahl, Philip, Holinski-Feder, Elke, Morak, Monika, Kloor, Matthias, Stemmler, Susanne, Betz, Beate, Hutter, Pierre, Bunyan, David J., Syngal, Sapna, Culver, Julie O., Graham, Tracy, Chan, Tsun L., Nagtegaal, Iris D., van Krieken, J. Han J.M, Schackert, Hans K., Hoogerbrugge, Nicoline, van Kessel, Ad Geurts, Ligtenberg, Marjolijn J.L.

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Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: Case series, review and follow-up guidelines von Herkert, Johanna C, Niessen, Renée C, Olderode-Berends, Maria J.W, Veenstra-Knol, Hermine E, Vos, Yvonne J, van der Klift, Heleen M, Scheenstra, Rene, Tops, Carli M.J, Karrenbeld, Arend, Peters, Frans T.M, Hofstra, Robert M.W, Kleibeuker, Jan H, Sijmons, Rolf H

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BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genes von Domingo, Enric, Niessen, Renée C, Oliveira, Carla, Alhopuro, Pia, Moutinho, Catia, Espín, Eloi, Armengol, Manel, Sijmons, Rolf H, Kleibeuker, Jan H, Seruca, Raquel, Aaltonen, Lauri A, Imai, Kohzoh, Yamamoto, Hiroyuki, Schwartz, Jr, Simó, Hofstra, Robert M W

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Low Tube Voltage Liver MDCT with Sinogram-Affirmed Iterative Reconstructions for the Detection of Hepatocellular Carcinoma von Pregler, B., Beyer, L. P., Teufel, A., Niessen, C., Stroszczynski, C., Brodoefel, H., Wiggermann, P.

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359: Role of the polarity protein Par3 in promotion and suppression of skin tumors von Kleefisch, D, Vorhagen, S, Niessen, C, Iden, S

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A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome) von Rump, P, Niessen, RC, Verbruggen, KT, Brouwer, OF, de Raad, M, Hordijk, R

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Age and learning during unemployment von Niessen, Cornelia

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