Chromosome instability is common in human cleavage-stage embryos von Vermeesch, Joris R, Vanneste, Evelyne, Voet, Thierry, Le Caignec, Cédric, Ampe, Michèle, Konings, Peter, Melotte, Cindy, Debrock, Sophie, Amyere, Mustapha, Vikkula, Miikka, Schuit, Frans, Fryns, Jean-Pierre, Verbeke, Geert, D'Hooghe, Thomas, Moreau, Yves

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DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis von Müller-Barth, Ursula, Olivares, José L, Glorieux, Francis, Wagenstaller, Janine, Benet-Pagès, Anna, Loris, César, Jüppner, Harald, Strom, Tim M, Bastepe, Murat, Kaiser, Stephanie M, Shlossberg, Alan H, Lorenz-Depiereux, Bettina, Amyere, Mustapha, Badenhoop, Klaus, Rittmaster, Roger S, Ramos, Feliciano J, Vikkula, Miikka

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Somatic Uniparental Isodisomy Explains Multifocality of Glomuvenous Malformations von Amyere, Mustapha, Aerts, Virginie, Brouillard, Pascal, McIntyre, Brendan A.S., Duhoux, François P., Wassef, Michel, Enjolras, Odile, Mulliken, John B., Devuyst, Olivier, Antoine-Poirel, Hélène, Boon, Laurence M., Vikkula, Miikka

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Molecular identification of aspartate N-acetyltransferase and its mutation in hypoacetylaspartia von Wiame, Elsa, Tyteca, Donatienne, Pierrot, Nathalie, Collard, François, Amyere, Mustapha, Noel, Gaëtane, Desmedt, Jonathan, Nassogne, Marie-Cécile, Vikkula, Miikka, Octave, Jean-Noël, Vincent, Marie-Françoise, Courtoy, Pierre J, Boltshauser, Eugen, van Schaftingen, Emile

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Constitutive macropinocytosis in oncogene-transformed fibroblasts depends on sequential permanent activation of phosphoinositide 3-kinase and phospholipase C von Amyere, M, Payrastre, B, Krause, U, Van Der Smissen, P, Veithen, A, Courtoy, P J

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Src Triggers Circular Ruffling and Macropinocytosis at the Apical Surface of Polarized MDCK Cells von Mettlen, Marcel, Platek, Anna, Van Der Smissen, Patrick, Carpentier, Sarah, Amyere, Mustapha, Lanzetti, Letizia, de Diesbach, Philippe, Tyteca, Donatienne, Courtoy, Pierre J.

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Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling von Amyere, Mustapha, Revencu, Nicole, Helaers, Raphaël, Pairet, Eleonore, Baselga, Eulalia, Cordisco, Maria, Chung, Wendy, Dubois, Josée, Lacour, Jean-Philippe, Martorell, Loreto, Mazereeuw-Hautier, Juliette, Pyeritz, Reed E, Amor, David J, Bisdorff, Annouk, Blei, Francine, Bombei, Hannah, Dompmartin, Anne, Brooks, David, Dupont, Juliette, González-Enseñat, Maria Antonia, Frieden, Ilona, Gérard, Marion, Kvarnung, Malin, Hanson-Kahn, Andrea Kwan, Hudgins, Louanne, Léauté-Labrèze, Christine, McCuaig, Catherine, Metry, Denise, Parent, Philippe, Paul, Carle, Petit, Florence, Phan, Alice, Quere, Isabelle, Salhi, Aicha, Turner, Anne, Vabres, Pierre, Vicente, Asuncion, Wargon, Orli, Watanabe, Shoji, Weibel, Lisa, Wilson, Ashley, Willing, Marcia, Mulliken, John B, Boon, Laurence M, Vikkula, Miikka

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TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation von Foulquier, François, Amyere, Mustapha, Jaeken, Jaak, Zeevaert, Renate, Schollen, Els, Race, Valérie, Bammens, Riet, Morelle, Willy, Rosnoblet, Claire, Legrand, Dominique, Demaegd, Didier, Buist, Neil, Cheillan, David, Guffon, Nathalie, Morsomme, Pierre, Annaert, Willem, Freeze, Hudson H., Van Schaftingen, Emile, Vikkula, Miikka, Matthijs, Gert

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v-Src accelerates spontaneous motility via phosphoinositide 3-kinase, phospholipase C and phospholipase D, but abrogates chemotaxis in Rat-1 and MDCK cells von Platek, Anna, Mettlen, Marcel, Camby, Isabelle, Kiss, Robert, Amyere, Mustapha, Courtoy, Pierre J

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KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation von Amyere, Mustapha, Vogt, Thomas, Hoo, Joe, Brandrup, Flemming, Bygum, Anette, Boon, Laurence, Vikkula, Miikka

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Giant cell tumor occurring in familial Paget's disease of bone: Report of clinical characteristics and linkage analysis of a large pedigree von Gianfrancesco, Fernando, Rendina, Domenico, Merlotti, Daniela, Esposito, Teresa, Amyere, Mustapha, Formicola, Daniela, Muscariello, Riccardo, De Filippo, Gianpaolo, Strazzullo, Pasquale, Nuti, Ranuccio, Vikkula, Mikka, Gennari, Luigi

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Germline loss-of-function mutations in EPHB4 cause a second form of capillary malformation-arteriovenous malformation (CM-AVM2) deregulating RAS-MAPK signaling von Amyere, Mustapha, Revencu, Nicole, Helaers, Raphaël, Pairet, Eleonore, Baselga, Eulalia, Cordisco, Maria, Chung, Wendy, Dubois, Josée, Lacour, Jean-Philippe, Martorell, Loreto, Mazereeuw-Hautier, Juliette, Pyeritz, Reed E, Amor, David J, Bisdorff, Annouk, Blei, Francine, Bombei, Hannah, Dompmartin, Anne, Brooks, David, Dupont, Juliette, González-Enseñat, Maria Antonia, Frieden, Ilona, Gérard, Marion, Kvarnung, Malin, Hanson-Kahn, Andrea Kwan, Hudgins, Louanne, Léauté-Labrèze, Christine, McCuaig, Catherine, Metry, Denise, Parent, Philippe, Paul, Carle, Weibel, Lisa, Vikkula, Miikka

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Regulation of macropinocytosis in v-Src-transformed fibroblasts: cyclic AMP selectively promotes regurgitation of macropinosomes von Veithen, A, Amyere, M, Van Der Smissen, P, Cupers, P, Courtoy, P J

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Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16 von Balikova, Irina, Martens, Kevin, Melotte, Cindy, Amyere, Mustapha, Van Vooren, Steven, Moreau, Yves, Vetrie, David, Fiegler, Heike, Carter, Nigel P., Liehr, Thomas, Vikkula, Miikka, Matthijs, Gert, Fryns, Jean-Pierre, Casteels, Ingele, Devriendt, Koen, Vermeesch, Joris Robert

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Origin, originality, functions, subversions and molecular signalling of macropinocytosis von AMYERE, Mustapha, METTLEN, Marcel, VAN DER SMISSEN, Patrick, PLATEK, Anna, PAYRASTRE, Bernard, VEITHEN, Alex, COURTOY, Pierre J

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Isolated bilateral transverse agenesis of the distal segments of the lower limbs at the level of the knee joint in a human fetus von Christiaens, Antoine B., Deprez, Pierre M. L., Amyere, Mustapha, Mendola, Antonella, Bernard, Pierre, Gillerot, Yves, Clapuyt, Philippe, Godfraind, Catherine, Lengelé, Benoît G., Vikkula, Miikka, Nyssen-Behets, Catherine

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Somatic uniparental isodisomy explains multifocality of glomuvenous malformations von Amyere, Mustapha, Aerts, Virginie, Brouillard, Pascal, McIntyre, Brendan A S, Duhoux, François P, Wassef, Michel, Enjolras, Odile, Mulliken, John B, Devuyst, Olivier, Antoine-Poirel, Hélène, Boon, Laurence M, Vikkula, Miikka

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Common Somatic Alterations Identified in Maffucci Syndrome by Molecular Karyotyping von Amyere, Mustapha, Dompmartin, Anne, Wouters, Vinciane, Enjolras, Odile, Kaitila, Ilkka, Docquier, Pierre-Louis, Godfraind, Catherine, Mulliken, John Butler, Boon, Laurence Myriam, Vikkula, Miikka

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Origin, originality, functions, subversions and molecular signalling of macropinocytosis von Amyere, Mustapha, Mettlen, Marcel, Van Der Smissen, Patrick, Platek, Anna, Payrastre, Bernard, Veithen, Alex, Courtoy, Pierre J.

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TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation von Foulquier, François, Amyere, Mustapha, Jaeken, Jaak, Zeevaert, Renate, Schollen, Els, Race, Valérie, Bammens, Riet, Morelle, Willy, Rosnoblet, Claire, Legrand, Dominique, Demaegd, Didier, Buist, Neil, Cheillan, David, Guffon, Nathalie, Morsomme, Pierre, Annaert, Wim, Freeze, Hudson H, Van Schaftingen, Emile, Vikkula, Miikka, Matthijs, Gert

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