Transcriptional Regulation of Osteoclastogenesis: The Emerging Role of KLF2 von Rolph, Daniela, Das, Hiranmoy

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Ferutinin directs dental pulp-derived stem cells towards the osteogenic lineage by epigenetically regulating canonical Wnt signaling von Rolph, Daniela N., Deb, Moonmoon, Kanji, Suman, Greene, Carl J., Das, Manjusri, Joseph, Matthew, Aggarwal, Reeva, Leblebicioglu, Binnaz, Das, Hiranmoy

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Ferutinin induces osteoblast differentiation of DPSCs via induction of KLF2 and autophagy/mitophagy von Maity, Jyotirindra, Barthels, Derek, Sarkar, Jaganmay, Prateeksha, Prateeksha, Deb, Moonmoon, Rolph, Daniela, Das, Hiranmoy

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Generation of Myocardial Ischemic Wounds and Healing with Stem Cells von Rolph, Daniela, Das, Hiranmoy

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Inhibiting p21-Activated Kinase Induces Cell Death in Vestibular Schwannoma and Meningioma via Mitotic Catastrophe von Mercado-Pimentel, Melania Ester, Miller, Craig, Rolph, Daniela N, Villalobos, Edrick F, Dunn, Allison M, Mohan, Prithvi M, Igarashi, Suzu, Liu, Xiangdang, Yrun-Duffy, Macken, Patel, Neal K, Read, Cecilia M, Francis, Ross H, Lane, Adelina Isabella, Murugesh, Swaroop, Jacob, Abraham

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Voltage-gated sodium channel scn8a is required for innervation and regeneration of amputated adult zebrafish fins von Osorio-Méndez, Daniel, Miller, Andrew, Begeman, Ian J, Kurth, Andrew, Hagle, Ryan, Rolph, Daniela, Dickson, Amy L, Chen, Chen-Hui, Halloran, Mary, Poss, Kenneth D, Kang, Junsu

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A novel MED12 mutation: Evidence for a fourth phenotype von Prontera, Paolo, Ottaviani, Valentina, Rogaia, Daniela, Isidori, Ilenia, Mencarelli, Amedea, Malerba, Natascia, Cocciadiferro, Dario, Rolph, Pfundt, Stangoni, Gabriela, Vulto-van Silfhout, Anneke, Merla, Giuseppe

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CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotype von Menke, Leonie A., van Belzen, Martine J., Alders, Marielle, Cristofoli, Francesca, Ehmke, Nadja, Fergelot, Patricia, Foster, Alison, Gerkes, Erica H., Hoffer, Mariëtte J. V., Horn, Denise, Kant, Sarina G., Lacombe, Didier, Leon, Eyby, Maas, Saskia M., Melis, Daniela, Muto, Valentina, Park, Soo-Mi, Peeters, Hilde, Peters, Dorien J. M., Pfundt, Rolph, van Ravenswaaij-Arts, Conny M. A., Tartaglia, Marco, Hennekam, Raoul C. M.

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Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders von Stolz, Jacob R., Foote, Kendall M., Veenstra-Knol, Hermine E., Pfundt, Rolph, ten Broeke, Sanne W., de Leeuw, Nicole, Roht, Laura, Pajusalu, Sander, Part, Reelika, Rebane, Ionella, Õunap, Katrin, Stark, Zornitza, Kirk, Edwin P., Lawson, John A., Lunke, Sebastian, Christodoulou, John, Louie, Raymond J., Rogers, R. Curtis, Davis, Jessica M., Innes, A. Micheil, Wei, Xing-Chang, Keren, Boris, Mignot, Cyril, Lebel, Robert Roger, Sperber, Steven M., Sakonju, Ai, Dosa, Nienke, Barge-Schaapveld, Daniela Q.C.M., Peeters-Scholte, Cacha M.P.C.D., Ruivenkamp, Claudia A.L., van Bon, Bregje W., Kennedy, Joanna, Low, Karen J., Ellard, Sian, Pang, Lewis, Junewick, Joseph J., Mark, Paul R., Carvill, Gemma L., Swanson, Geoffrey T.

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Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf‐Hirschhorn syndrome–associated seizures disorder von Zollino, Marcella, Orteschi, Daniela, Ruiter, Mariken, Pfundt, Rolph, Steindl, Katharina, Cafiero, Concetta, Ricciardi, Stefania, Contaldo, Ilaria, Chieffo, Daniela, Ranalli, Domiziana, Acquafondata, Celeste, Murdolo, Marina, Marangi, Giuseppe, Asaro, Alessia, Battaglia, Domenica

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Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features von Turnpenny, Peter D., Wright, Michael J., Sloman, Melissa, Caswell, Richard, van Essen, Anthony J., Gerkes, Erica, Pfundt, Rolph, White, Susan M., Shaul-Lotan, Nava, Carpenter, Lori, Schaefer, G. Bradley, Fryer, Alan, Innes, A. Micheil, Forbes, Kirsten P., Chung, Wendy K., McLaughlin, Heather, Henderson, Lindsay B., Roberts, Amy E., Heath, Karen E., Paumard-Hernández, Beatriz, Gener, Blanca, Fawcett, Katherine A., Gjergja-Juraški, Romana, Pilz, Daniela T., Fry, Andrew E.

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De Novo Variants in SPOP Cause Two Clinically Distinct Neurodevelopmental Disorders von Nabais Sá, Maria J., El Tekle, Geniver, de Brouwer, Arjan P.M., Sawyer, Sarah L., del Gaudio, Daniela, Parker, Michael J., Kanani, Farah, van den Boogaard, Marie-José H., van Gassen, Koen, Van Allen, Margot I., Wierenga, Klaas, Purcarin, Gabriela, Elias, Ellen Roy, Begtrup, Amber, Keller-Ramey, Jennifer, Bernasocchi, Tiziano, van de Wiel, Laurens, Gilissen, Christian, Venselaar, Hanka, Pfundt, Rolph, Vissers, Lisenka E.L.M., Theurillat, Jean-Philippe P., de Vries, Bert B.A.

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Targeted Next-Generation Sequencing Appoints C16orf57 as Clericuzio-Type Poikiloderma with Neutropenia Gene von Volpi, Ludovica, Roversi, Gaia, Colombo, Elisa Adele, Leijsten, Nico, Concolino, Daniela, Calabria, Andrea, Mencarelli, Maria Antonietta, Fimiani, Michele, Macciardi, Fabio, Pfundt, Rolph, Schoenmakers, Eric F.P.M., Larizza, Lidia

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De Novo Variants in SPOP Cause Two Clinically Distinct Neurodevelopmental Disorders von Nabais Sá, Maria J, El Tekle, Geniver, de Brouwer, Arjan P.M, Sawyer, Sarah L, del Gaudio, Daniela, Parker, Michael J, Kanani, Farah, van den Boogaard, Marie José H, van Gassen, Koen, Van Allen, Margot I, Wierenga, Klaas, Purcarin, Gabriela, Elias, Ellen Roy, Begtrup, Amber, Keller-Ramey, Jennifer, Bernasocchi, Tiziano, van de Wiel, Laurens, Gilissen, Christian, Venselaar, Hanka, Pfundt, Rolph, Vissers, Lisenka E.L.M, Theurillat, Jean Philippe P, de Vries, Bert B.A

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Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features von Turnpenny, Peter D., Wright, Michael J., Sloman, Melissa, Caswell, Richard, van Essen, Anthony J., Gerkes, Erica, Pfundt, Rolph, White, Susan M., Shaul-Lotan, Nava, Carpenter, Lori, Schaefer, G. Bradley, Fryer, Alan, Innes, A. Micheil, Forbes, Kirsten P., Chung, Wendy K., McLaughlin, Heather, Henderson, Lindsay B., Roberts, Amy E., Heath, Karen E., Paumard-Hernández, Beatriz, Gener, Blanca, Fawcett, Katherine A., Gjergja-Juraški, Romana, Pilz, Daniela T., Fry, Andrew E.

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Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder von Zollino, Marcella, Orteschi, Daniela, Ruiter, Mariken, Pfundt, Rolph, Steindl, Katharina, Cafiero, Concetta, Ricciardi, Stefania, Contaldo, Ilaria, Chieffo, Daniela, Ranalli, Domiziana, Acquafondata, Celeste, Murdolo, Marina, Marangi, Giuseppe, Asaro, Alessia, Battaglia, Domenica

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The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype von van Bon, Bregje WM, Koolen, David A, Brueton, Louise, McMullan, Dominic, Lichtenbelt, Klaske D, Adès, Lesley C, Peters, Gregory, Gibson, Kate, Novara, Francesca, Pramparo, Tiziano, Bernardina, Bernardo Dalla, Zoccante, Leonardo, Balottin, Umberto, Piazza, Fausta, Pecile, Vanna, Gasparini, Paolo, Guerci, Veronica, Kets, Marleen, Pfundt, Rolph, de Brouwer, Arjan P, Veltman, Joris A, de Leeuw, Nicole, Wilson, Meredith, Antony, Jayne, Reitano, Santina, Luciano, Daniela, Fichera, Marco, Romano, Corrado, Brunner, Han G, Zuffardi, Orsetta, de Vries, Bert BA

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CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotype von Menke, Leonie A, van Belzen, Martine J, Alders, Marielle, Cristofoli, Francesca, Ehmke, Nadja, Fergelot, Patricia, Foster, Alison, Gerkes, Erica H, Hoffer, Mariëtte J.V, Horn, Denise, Kant, Sarina G, Lacombe, Didier, Leon, Eyby, Maas, Saskia M, Melis, Daniela, Muto, Valentina, Park, Soo-Mi, Peeters, Hilde, Peters, Dorien J.M, Pfundt, Rolph, van Ravenswaaij-Arts, Conny M.A, Tartaglia, Marco, Hennekam, Raoul C.M

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Targeted Next-Generation Sequencing Appoints C16orf57 as Clericuzio-Type Poikiloderma with Neutropenia Gene von Volpi, Ludovica, Roversi, Gaia, Colombo, Elisa Adele, Leijsten, Nico, Concolino, Daniela, Calabria, Andrea, Mencarelli, Maria Antonietta, Fimiani, Michele, Macciardi, Fabio, Pfundt, Rolph, Schoenmakers, Eric F.P.M., Larizza, Lidia

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Erratum: The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype von van Bon, Bregje W M, Koolen, David A, Brueton, Louise, McMullan, Dominic, Lichtenbelt, Klaske D, Adès, Lesley C, Peters, Gregory, Gibson, Kate, Moloney, Susan, Novara, Francesca, Pramparo, Tiziano, Bernardina, Bernardo Dalla, Zoccante, Leonardo, Balottin, Umberto, Piazza, Fausta, Pecile, Vanna, Gasparini, Paolo, Guerci, Veronica, Kets, Marleen, Pfundt, Rolph, de Brouwer, Arjan P, Veltman, Joris A, de Leeuw, Nicole, Wilson, Meredith, Antony, Jayne, Reitano, Santina, Luciano, Daniela, Fichera, Marco, Romano, Corrado, Brunner, Han G, Zuffardi, Orsetta, de Vries, Bert BA

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