Diverse diseases from a ubiquitous process: The ribosomopathy paradox by Armistead, Joy, Triggs-Raine, Barbara

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NAMPT-derived NAD+ fuels PARP1 to promote skin inflammation through parthanatos cell death by Martínez-Morcillo, Francisco J, Cantón-Sandoval, Joaquín, Martínez-Navarro, Francisco J, Cabas, Isabel, Martínez-Vicente, Idoya, Armistead, Joy, Hatzold, Julia, López-Muñoz, Azucena, Martínez-Menchón, Teresa, Corbalán-Vélez, Raúl, Lacal, Jesús, Hammerschmidt, Matthias, García-Borrón, José C, García-Ayala, Alfonsa, Cayuela, María L, Pérez-Oliva, Ana B, García-Moreno, Diana, Mulero, Victoriano

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Hemicentin-1 is an essential extracellular matrix component of the dermal–epidermal and myotendinous junctions by Welcker, Daniela, Stein, Cornelia, Feitosa, Natalia Martins, Armistead, Joy, Zhang, Jin-Li, Lütke, Steffen, Kleinridders, Andre, Brüning, Jens C., Eming, Sabine A., Sengle, Gerhard, Niehoff, Anja, Bloch, Wilhelm, Hammerschmidt, Matthias

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Matriptase-dependent epidermal pre-neoplasm in zebrafish embryos caused by a combination of hypotonic stress and epithelial polarity defects by Hatzold, Julia, Nett, Verena, Brantsch, Stephanie, Zhang, Jin-Li, Armistead, Joy, Wessendorf, Heike, Stephens, Rebecca, Humbert, Patrick O, Iden, Sandra, Hammerschmidt, Matthias

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A sphingolipid rheostat controls apoptosis versus apical cell extrusion as alternative tumour-suppressive mechanisms by Armistead, Joy, Höpfl, Sebastian, Goldhausen, Pierre, Müller-Hartmann, Andrea, Fahle, Evelin, Hatzold, Julia, Franzen, Rainer, Brodesser, Susanne, Radde, Nicole E., Hammerschmidt, Matthias

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Mutation of a Gene Essential for Ribosome Biogenesis, EMG1, Causes Bowen-Conradi Syndrome by Armistead, Joy, Khatkar, Sunita, Meyer, Britta, Mark, Brian L., Patel, Nehal, Coghlan, Gail, Lamont, Ryan E., Liu, Shuangbo, Wiechert, Jill, Cattini, Peter A., Koetter, Peter, Wrogemann, Klaus, Greenberg, Cheryl R., Entian, Karl-Dieter, Zelinski, Teresa, Triggs-Raine, Barbara

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NAMPT-derived NAD+ fuels PARP1 to promote skin inflammation through parthanatos cell death by Francisco J Martínez-Morcillo, Joaquín Cantón-Sandoval, Francisco J Martínez-Navarro, Isabel Cabas, Idoya Martínez-Vicente, Joy Armistead, Julia Hatzold, Azucena López-Muñoz, Teresa Martínez-Menchón, Raúl Corbalán-Vélez, Jesús Lacal, Matthias Hammerschmidt, José C García-Borrón, Alfonsa García-Ayala, María L Cayuela, Ana B Pérez-Oliva, Diana García-Moreno, Victoriano Mulero

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Growth arrest in the ribosomopathy, Bowen–Conradi syndrome, is due to dramatically reduced cell proliferation and a defect in mitotic progression by Armistead, Joy, Patel, Nehal, Wu, Xiaoli, Hemming, Richard, Chowdhury, Biswajit, Basra, Gagandeep Singh, Del Bigio, Marc R., Ding, Hao, Triggs-Raine, Barbara

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The adult polyglucosan body disease mutation GBE1 c.1076A>C occurs at high frequency in persons of Ashkenazi Jewish background by Hussain, Abrar, Armistead, Joy, Gushulak, Lara, Kruck, Christa, Pind, Steven, Triggs-Raine, Barbara, Natowicz, Marvin R.

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Mutation of EMG1 causing Bowen–Conradi syndrome results in reduced cell proliferation rates concomitant with G2/M arrest and 18S rRNA processing delay by Armistead, Joy, Hemming, Richard, Patel, Nehal, Triggs-Raine, Barbara

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Antibodies to a Single, Conserved Epitope in Anopheles APN1 Inhibit Universal Transmission of Plasmodium falciparum and Plasmodium vivax Malaria by Armistead, Jennifer S, Morlais, Isabelle, Mathias, Derrick K, Jardim, Juliette G, Joy, Jaimy, Fridman, Arthur, Finnefrock, Adam C, Bagchi, Ansu, Plebanski, Magdalena, Scorpio, Diana G, Churcher, Thomas S, Borg, Natalie A, Sattabongkot, Jetsumon, Dinglasan, Rhoel R

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