Porokeratotic Eccrine Nevus May Be Caused by Somatic Connexin26 Mutations von Easton, Jennifer A., Donnelly, Steven, Kamps, Miriam A.F., Steijlen, Peter M., Martin, Patricia E., Tadini, Gianluca, Janssens, René, Happle, Rudolf, van Geel, Michel, van Steensel, Maurice A.M.

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Cellular strain avoidance is mediated by a functional actin cap - observations in an Lmna -deficient cell model von Tamiello, Chiara, Halder, Maurice, Kamps, Miriam A F, Baaijens, Frank P T, Broers, Jos L V, Bouten, Carlijn V C

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Birt-Hogg-Dube syndrome is a novel ciliopathy von Luijten, Monique N H, Basten, Sander G, Claessens, Tijs, Vernooij, Marigje, Scott, Claire L, Janssen, Renske, Easton, Jennifer A, Kamps, Miriam A F, Vreeburg, Maaike, Broers, Jos L V, van Geel, Michel, Menko, Fred H, Harbottle, Richard P, Nookala, Ravi K, Tee, Andrew R, Land, Stephen C, Giles, Rachel H, Coull, Barry J, van Steensel, Maurice A M

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HPV in situ hybridization: Impact of different protocols on the detection of integrated HPV von Hopman, Anton H.N., Kamps, Miriam A., Smedts, Frank, Speel, Ernst‐Jan M., Herrington, C. Simon, Ramaekers, Frans C.S.

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Assessment of fibroblast nuclear morphology aids interpretation of LMNA variants von van Tienen, Florence H J, Lindsey, Patrick J, Kamps, Miriam A F, Krapels, Ingrid P, Ramaekers, Frans C S, Brunner, Han G, van den Wijngaard, Arthur, Broers, Jos L V

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A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell death von Easton, Jennifer A., Albuloushi, Ahmad K., Kamps, Miriam A. F., Brouns, Gladys H. M. R., Broers, Jos L. V., Coull, Barry J., Oji, Vincent, van Geel, Michel, van Steensel, Maurice A. M., Martin, Patricia E.

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Identification of Chromosome 9 Alterations and p53 Accumulation in Isolated Carcinoma in Situ of the Urinary Bladder versus Carcinoma in Situ Associated with Carcinoma von Hopman, Anton H.N., Kamps, Miriam A.F., Speel, Ernst J.M., Schapers, Rene F.M., Sauter, Guido, Ramaekers, Frans C.S.

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FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation von Dunlop, Elaine A, Seifan, Sara, Claessens, Tijs, Behrends, Christian, Kamps, Miriam AF, Rozycka, Ewelina, Kemp, Alain J, Nookala, Ravi K, Blenis, John, Coull, Barry J, Murray, James T, van Steensel, Maurice AM, Wilkinson, Simon, Tee, Andrew R

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Soft substrates normalize nuclear morphology and prevent nuclear rupture in fibroblasts from a laminopathy patient with compound heterozygous LMNA mutations von Tamiello, Chiara, Kamps, Miriam A.F., van den Wijngaard, Arthur, Verstraeten, Valerie L. R. M., Baaijens, Frank P.T., Broers, Jos L.V., Bouten, Carlijn C.V.

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Molecular analysis of connexin26 asparagine14 mutations associated with syndromic skin phenotypes von de Zwart-Storm, Eugene A., Rosa, Rafael F. M., Martin, Patricia E., Foelster-Holst, Regina, Frank, Jorge, Bau, Ana E. K., Zen, Paulo R. G., Graziadio, Carla, Paskulin, Giorgio A., Kamps, Miriam A., van Geel, Michel, van Steensel, Maurice A. M.

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Molecular analysis of connexin26 asparagine14 mutations associated with syndromic skin phenotypes: Molecular analysis of connexin26 asparagine14 mutations von de Zwart-Storm, Eugene A., Rosa, Rafael F. M., Martin, Patricia E., Foelster-Holst, Regina, Frank, Jorge, Bau, Ana E. K., Zen, Paulo R. G., Graziadio, Carla, Paskulin, Giorgio A., Kamps, Miriam A., van Geel, Michel, van Steensel, Maurice A. M.

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No HLA-A gene detectable on one of the haplotypes in a caucasian family von Swelsen, Wendy T.N., Voorter, Christina E.M., Tilanus, Marcel G.J., Kamps, Miriam A.F., van den Berg-Loonen, Ella M.

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The tumor suppressor folliculin regulates AMPK-dependent metabolic transformation von Yan, Ming, Gingras, Marie-Claude, Dunlop, Elaine A, Nouët, Yann, Dupuy, Fanny, Jalali, Zahra, Possik, Elite, Coull, Barry J, Kharitidi, Dmitri, Dydensborg, Anders Bondo, Faubert, Brandon, Kamps, Miriam, Sabourin, Sylvie, Preston, Rachael S, Davies, David Mark, Roughead, Taren, Chotard, Laëtitia, van Steensel, Maurice A M, Jones, Russell, Tee, Andrew R, Pause, Arnim

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Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies von De Vos, Winnok H., Houben, Frederik, Kamps, Miriam, Malhas, Ashraf, Verheyen, Fons, Cox, Juliën, Manders, Erik M.M., Verstraeten, Valerie L.R.M., van Steensel, Maurice A.M., Marcelis, Carlo L.M., van den Wijngaard, Arthur, Vaux, David J., Ramaekers, Frans C.S., Broers, Jos L.V.

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Severe Pediatric COVID-19 and Multisystem Inflammatory Syndrome in Children from Wild-type to Population Immunity: A Prospective Multicenter Cohort Study with Real-time Reporting von Tulling, Adam J, Lugthart, Gertjan, Mooij, Miriam G, Brackel, Caroline L.H, Terheggen-Lagro, Suzanne W.J, Oostenbrink, Rianne, Buysse, Corinne M.P, Hashimoto, Simone, Armbrust, Wineke, Bannier, Michiel A.G.E, Bekhof, Jolita, Van Gameren-Oosterom, Helma B, Hendriks, Han, Van Houten, Marlies A, Van Der Linden, Jan W, Lebon, Ankie, Van Onzenoort-Bokken, Lonneke, Tramper-Stranders, Gerdien A, Van Veen, Mirjam, Von Asmuth, Erik G.J, Buddingh, Emilie P, Van Der Aa, Leontien B, Van Aerde, Koen J, Auffarth-Smedema, Bettina, Bart, Ingeborg Y, Beek, Cherise, Bechan, Gitanjali I, Van Den Berg, J. Merlijn, Boonstra, Venje H, Breukels, Mijke, Brinkman, Danielle M.C, Bruijning-Verhagen, Patricia C.J.L, De Crom, Stephanie C, Ernst-Kruis, Margot R, Fraaij, Pieter L.A, Goris, Joyce, Groeneweg, Michael, Gruppen, Mariken, Hammer, Sanne C, Hissink Muller, Petra C.E, Homan-Van Der Veen, Jenneke, Jacobs, Monique A.M, Kamps, Arvid W.A, Ketharanathan, Naomi, Van Der Kuip, Martijn, Kuijpers, Taco W, Legger, Elizabeth G, Lo-A-Njoe, Shirley, Manshande, Meindert E, Miedema, Carien J, Obihara, Charlie C, Olivieira, Gideon O, Oudshoorn, Annemarie, Peeters, Esther J.E, Petru, Ronald, Pijnenburg, Marielle W.H, Rook, Denise, Schilleman, Kim, Schopmeijer, Rian, Slotboom, David, Van Der Steen, Manouk, Stol, Kim, Thomasse, Yolande E.M, Tissing, Wim J.E, Van Den Tweel, Xandra W, Vastert, Sebastiaan J, Verbeek, Anne B, Vernooij-Van Langen, Annette M.M, Wieringa, Jantien W, Wildenbeest, Joanne G, De Wildt, Saskia N, Van Woerden, Christiaan

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Reorganization of the nuclear lamina and cytoskeleton in adipogenesis von Verstraeten, Valerie L. R. M, Renes, Johan, Ramaekers, Frans C. S, Kamps, Miriam, Kuijpers, Helma J, Verheyen, Fons, Wabitsch, Martin, Steijlen, Peter M, van Steensel, Maurice A. M, Broers, Jos L. V

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Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation von Verstraeten, Valerie L.R.M., Broers, Jos L.V., van Steensel, Maurice A.M., Zinn-Justin, Sophie, Ramaekers, Frans C.S., Steijlen, Peter M., Kamps, Miriam, Kuijpers, Helma J.H., Merckx, Diane, Smeets, Hubert J.M., Hennekam, Raoul C.M., Marcelis, Carlo L.M., van den Wijngaard, Arthur

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The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress von Verstraeten, Valerie L.R.M., Caputo, Sandrine, Van Steensel, Maurice A.M., Duband‐Goulet, Isabelle, Zinn‐Justin, Sophie, Kamps, Miriam, Kuijpers, Helma J.H., Östlund, Cecilia, Worman, Howard J., Briedé, Jacob J., Le Dour, Caroline, Marcelis, Carlo L.M., Van Geel, Michel, Steijlen, Peter M., Van Den Wijngaard, Arthur, Ramaekers, Frans C.S., Broers, Jos L.V.

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Multicolour preparations for in situ hybridization using precipitating enzyme cytochemistry in combination with reflection contrast microscopy von Speel, Ernst J. M., Kamps, Miriam, Bonnet, Jan, Ramaekers, Frans C. S., Hopman, Anton H. N.

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