Cryptochrome: The magnetosensor with a sinister side? von Landler, Lukas, Keays, David A

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Myths in magnetosensation von Nimpf, Simon, Keays, David A.

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Improved Genome Assembly and Annotation for the Rock Pigeon (Columba livia) von Holt, Carson, Campbell, Michael, Keays, David A, Edelman, Nathaniel, Kapusta, Aurélie, Maclary, Emily, T. Domyan, Eric, Suh, Alexander, Warren, Wesley C, Yandell, Mark, Gilbert, M Thomas P, Shapiro, Michael D

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No evidence for intracellular magnetite in putative vertebrate magnetoreceptors identified by magnetic screening von Edelman, Nathaniel B., Fritz, Tanja, Nimpf, Simon, Pichler, Paul, Lauwers, Mattias, Hickman, Robert W., Papadaki-Anastasopoulou, Artemis, Ushakova, Lyubov, Heuser, Thomas, Resch, Guenter P., Saunders, Martin, Shaw, Jeremy A., Keays, David A.

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Mutations in PGAP3 Impair GPI-Anchor Maturation, Causing a Subtype of Hyperphosphatasia with Mental Retardation von Howard, Malcolm F., Murakami, Yoshiko, Pagnamenta, Alistair T., Daumer-Haas, Cornelia, Fischer, Björn, Hecht, Jochen, Keays, David A., Knight, Samantha J.L., Kölsch, Uwe, Krüger, Ulrike, Leiz, Steffen, Maeda, Yusuke, Mitchell, Daphne, Mundlos, Stefan, Phillips, John A., Robinson, Peter N., Kini, Usha, Taylor, Jenny C., Horn, Denise, Kinoshita, Taroh, Krawitz, Peter M.

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MAPping tubulin mutations von Cushion, Thomas D, Leca, Ines, Keays, David A

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The biophysical, molecular, and anatomical landscape of pigeon CRY4: A candidate light-based quantal magnetosensor von Hochstoeger, Tobias, Al Said, Tarek, Maestre, Dante, Walter, Florian, Vilceanu, Alexandra, Pedron, Miriam, Cushion, Thomas D, Snider, William, Nimpf, Simon, Nordmann, Gregory Charles, Landler, Lukas, Edelman, Nathaniel, Kruppa, Lennard, Dürnberger, Gerhard, Mechtler, Karl, Schuechner, Stefan, Ogris, Egon, Malkemper, E Pascal, Weber, Stefan, Schleicher, Erik, Keays, David A

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Magnetoreception-A sense without a receptor von Nordmann, Gregory C, Hochstoeger, Tobias, Keays, David A

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Low-intensity electromagnetic fields induce human cryptochrome to modulate intracellular reactive oxygen species von Sherrard, Rachel M, Morellini, Natalie, Jourdan, Nathalie, El-Esawi, Mohamed, Arthaut, Louis-David, Niessner, Christine, Rouyer, Francois, Klarsfeld, Andre, Doulazmi, Mohamed, Witczak, Jacques, d'Harlingue, Alain, Mariani, Jean, Mclure, Ian, Martino, Carlos F, Ahmad, Margaret

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Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene von CONTI, Valerio, CARABALONA, Aurelie, WATRIN, Françoise, LISE, Stefano, PAGNAMENTA, Alistair T, TAYLOR, Jenny C, KINI, Usha, CLAYTON-SMITH, Jill, NOVARA, Francesca, ZUFFARDI, Orsetta, DOBYNS, William B, SCHEFFER, Ingrid E, PALLESI-POCACHARD, Emilie, ROBERTSON, Stephen P, BERKOVIC, Samuel F, REPRESA, Alfonso, KEAYS, David A, CARDOSO, Carlos, GUERRINI, Renzo, PARRINI, Elena, LEVENTER, Richard J, BUHLER, Emmanuelle, MCGILLIVRAY, George, MICHEL, François J, STRIANO, Pasquale, MEI, Davide

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The expression, localisation and interactome of pigeon CRY2 von Balay, Spencer D., Hochstoeger, Tobias, Vilceanu, Alexandra, Malkemper, E. Pascal, Snider, William, Dürnberger, Gerhard, Mechtler, Karl, Schuechner, Stefan, Ogris, Egon, Nordmann, Gregory C., Ushakova, Lyubov, Nimpf, Simon, Keays, David A.

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Is magnetogenetics the new optogenetics? von Nimpf, Simon, Keays, David A

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Why (and how) we should publish negative data von Nimpf, Simon, Keays, David A

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Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A) von Poirier, Karine, Keays, David A, Francis, Fiona, Saillour, Yoann, Bahi, Nadia, Manouvrier, Sylvie, Fallet-Bianco, Catherine, Pasquier, Laurent, Toutain, Annick, Tuy, Françoise Phan Dinh, Bienvenu, Thierry, Joriot, Sylvie, Odent, Sylvie, Ville, Dorothée, Desguerre, Isabelle, Goldenberg, Alice, Moutard, Marie-Laure, Fryns, Jean-Pierre, van Esch, Hilde, Harvey, Robert J, Siebold, Christian, Flint, Jonathan, Beldjord, Chérif, Chelly, Jamel

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Unsolved mysteries: Magnetoreception-A sense without a receptor von Nordmann, Gregory C, Hochstoeger, Tobias, Keays, David A

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Tuba8 Is Expressed at Low Levels in the Developing Mouse and Human Brain von Braun, Andreas, Breuss, Martin, Salzer, Marion C., Flint, Jonathan, Cowan, Nicholas J., Keays, David A.

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Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway von Tian, Guoling, Jaglin, Xavier H., Keays, David A., Francis, Fiona, Chelly, Jamel, Cowan, Nicholas J.

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De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation von Haas, Matilda A., Ngo, Linh, Li, Shan Shan, Schleich, Sibylle, Qu, Zhengdong, Vanyai, Hannah K., Cullen, Hayley D., Cardona-Alberich, Aida, Gladwyn-Ng, Ivan E., Pagnamenta, Alistair T., Taylor, Jenny C., Stewart, Helen, Kini, Usha, Duncan, Kent E., Teleman, Aurelio A., Keays, David A., Heng, Julian I.-T.

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The expression of tubb2b undergoes a developmental transition in murine cortical neurons von Breuss, Martin, Morandell, Jasmin, Nimpf, Simon, Gstrein, Thomas, Lauwers, Mattias, Hochstoeger, Tobias, Braun, Andreas, Chan, Kelvin, Sánchez Guajardo, Edmundo R., Zhang, Lijuan, Suplata, Marek, Heinze, Katrin G., Elsayad, Kareem, Keays, David A.

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Comment on "Magnetosensitive neurons mediate geomagnetic orientation in Caenorhabditis elegans" von Landler, Lukas, Nimpf, Simon, Hochstoeger, Tobias, Nordmann, Gregory C, Papadaki-Anastasopoulou, Artemis, Keays, David A

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