 |  |  |  |  | Table of ContentsNews & Views Articles Corrigendum | Volume 35, Number 8 | News & Views  | New structural work on the selectivity filter of voltage‐gated sodium channels explains their striking cation preferences. Werner Kühlbrandt Published online 21.03.2016 |  | A tractable new mouse model for Aicardi–Goutières syndrome (AGS) implicates the cGAS‐STING pathway for cytosolic nucleic acid sensing in this auto‐inflammatory disease. Matteo Gentili and Nicolas Manel Published online 23.03.2016 |  | A new study demonstrates the impact of disease‐linked PDI mutations on motoneuron function. Niran Maharjan and Smita Saxena Published online 11.03.2016 |  | c‐Myc and N‐Myc are dispensable for the control of pluripotency in embryonic stem cells and diapause—a state of suspension during embryonic development, but control reversible entry and exit from dormancy by governing biosynthesis and metabolism. Masato Nakagawa, Peter Karagiannis, and Shinya Yamanaka Published online 10.03.2016 | Articles  | Mutations in centrosomal‐P4.1‐associated protein (CPAP) cause Seckel syndrome. CPAP defects prevent proper cilium disassembly in neural progenitor cells with cell cycle progression delay and premature differentiation, leading to the microcephaly associated with this syndrome. Elke Gabriel, Arpit Wason, Anand Ramani, Li Ming Gooi, Patrick Keller, Andrei Pozniakovsky, Ina Poser, Florian Noack, Narasimha Swamy Telugu, Federico Calegari, Tomo Šarić, Jürgen Hescheler, Anthony A Hyman, Marco Gottardo, Giuliano Callaini, Fowzan Sami Alkuraya, and Jay Gopalakrishnan |  | Structural localisation of sodium ions passing through the prokaryotic NavM channel selectivity filter explains this channel's strong sodium preference over other cations in electrochemical signalling across cell membranes. Claire E Naylor, Claire Bagnéris, Paul G DeCaen, Altin Sula, Antonella Scaglione, David E Clapham, and BA Wallace |  | A new mouse model reveals the key nucleic acid‐sensing and signalling pathway in autoinflammatory Aicardi–Goutières syndrome caused by RNase H2 mutations. Karen J Mackenzie, Paula Carroll, Laura Lettice, Žygimantė Tarnauskaitė, Kaalak Reddy, Flora Dix, Ailsa Revuelta, Erika Abbondati, Rachel E Rigby, Björn Rabe, Fiona Kilanowski, Graeme Grimes, Adeline Fluteau, Paul S Devenney, Robert E Hill, Martin AM Reijns, and Andrew P Jackson |  | Disease phenotypes associated with expression of mutant PDIA1 and ERp57 show how impaired ER proteostasis can drive initial stages of amyotrophic lateral sclerosis pathology. Ute Woehlbier, Alicia Colombo, Mirva J Saaranen, Viviana Pérez, Jorge Ojeda, Fernando J Bustos, Catherine I Andreu, Mauricio Torres, Vicente Valenzuela, Danilo B Medinas, Pablo Rozas, Rene L Vidal, Rodrigo Lopez‐Gonzalez, Johnny Salameh, Sara Fernandez‐Collemann, Natalia Muñoz, Soledad Matus, Ricardo Armisen, Alfredo Sagredo, Karina Palma, Thergiory Irrazabal, Sandra Almeida, Paloma Gonzalez‐Perez, Mario Campero, Fen‐Biao Gao, Pablo Henny, Brigitte van Zundert, Lloyd W Ruddock, Miguel L Concha, Juan P Henriquez, Robert H Brown, and Claudio Hetz Published online 11.02.2016 |  | USP19 stabilizes Beclin‐1 by cleaving K11‐linked ubiquitin chains on Beclin‐1, thereby promoting autophagy and inhibiting the type I IFN signaling pathway. Shouheng Jin, Shuo Tian, Yamei Chen, Chuanxia Zhang, Weihong Xie, Xiaojun Xia, Jun Cui, and Rong‐Fu Wang Published online 17.03.2016 |  | Expression of the master Tfh cell differentiation factor Bcl6 is controlled by Bob1 and Oct1/2 transcription factors, to fine‐tune B‐cell responses following antigen‐mediated immunization. Dennis Stauss, Cornelia Brunner, Friederike Berberich‐Siebelt, Uta E Höpken, Martin Lipp, and Gerd Müller | Corrigendum  | Jin Zhang, Ivan Khvorostov, Jason S Hong, Yavuz Oktay, Laurent Vergnes, Esther Nuebel, Paulin N Wahjudi, Kiyoko Setoguchi, Geng Wang, Anna Do, Hea‐Jin Jung, J Michael McCaffery, Irwin J Kurland, Karen Reue, Wai‐Nang P Lee, Carla M Koehler, and Michael A Teitell Published online 15.04.2016 | |  | | |
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