Neuronal migration: unraveling the molecular pathway with humans, mice, and a fungus

av Keays, David A.
Publicerad 2007

Is magnetogenetics the new optogenetics?

av Nimpf, Simon, Keays, David A
I publikationen EMBO J (2017)

Cryptochrome: The magnetosensor with a sinister side?

av Landler, Lukas, Keays, David A.
I publikationen PLoS Biol (2018)

Why (and how) we should publish negative data

av Nimpf, Simon, Keays, David A
I publikationen EMBO Rep (2019)

Magnetoreception—A sense without a receptor

av Nordmann, Gregory C., Hochstoeger, Tobias, Keays, David A.
I publikationen PLoS Biol (2017)

Ectopic otoconial formation in the lagena of the pigeon inner ear

av Malkemper, E. Pascal, Mason, Matthew J., Kagerbauer, Daniel, Nimpf, Simon, Keays, David A.
I publikationen Biol Open (2018)

Tuba8 Is Expressed at Low Levels in the Developing Mouse and Human Brain

av Braun, Andreas, Breuss, Martin, Salzer, Marion C., Flint, Jonathan, Cowan, Nicholas J., Keays, David A.
Publicerad 2010

Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway

av Tian, Guoling, Jaglin, Xavier H., Keays, David A., Francis, Fiona, Chelly, Jamel, Cowan, Nicholas J.
Publicerad 2010

Comment on "Magnetosensitive neurons mediate geomagnetic orientation in Caenorhabditis elegans"

av Landler, Lukas, Nimpf, Simon, Hochstoeger, Tobias, Nordmann, Gregory C, Papadaki-Anastasopoulou, Artemis, Keays, David A
I publikationen eLife (2018)

Activation of an exonic splice‐donor site in exon 30 of CDK5RAP2 in a patient with severe microcephaly and pigmentary abnormalities

av Pagnamenta, Alistair T., Howard, Malcolm F., Knight, Samantha J. L., Keays, David A., Quaghebeur, Gerardine, Taylor, Jenny C., Kini, Usha
I publikationen Clin Case Rep (2016)

Subcellular analysis of pigeon hair cells implicates vesicular trafficking in cuticulosome formation and maintenance

av Nimpf, Simon, Malkemper, Erich Pascal, Lauwers, Mattias, Ushakova, Lyubov, Nordmann, Gregory, Wenninger-Weinzierl, Andrea, Burkard, Thomas R, Jacob, Sonja, Heuser, Thomas, Resch, Guenter P, Keays, David A
I publikationen eLife (2017)

Germline recessive mutations in PI4KA are associated with perisylvian polymicrogyria, cerebellar hypoplasia and arthrogryposis

av Pagnamenta, Alistair T., Howard, Malcolm F., Wisniewski, Eva, Popitsch, Niko, Knight, Samantha J.L., Keays, David A., Quaghebeur, Gerardine, Cox, Helen, Cox, Phillip, Balla, Tamas, Taylor, Jenny C., Kini, Usha
I publikationen Hum Mol Genet (2015)

Improved Genome Assembly and Annotation for the Rock Pigeon (Columba livia)

av 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.
I publikationen G3 (Bethesda) (2018)

A Novel Nonsense CDK5RAP2 Mutation in a Somali Child With Primary Microcephaly and Sensorineural Hearing Loss

av Pagnamenta, Alistair T, Murray, Jennie E, Yoon, Grace, Akha, Elham Sadighi, Harrison, Victoria, Bicknell, Louise S, Ajilogba, Kaseem, Stewart, Helen, Kini, Usha, Taylor, Jenny C, Keays, David A, Jackson, Andrew P, Knight, Samantha JL
Publicerad 2012

No evidence for intracellular magnetite in putative vertebrate magnetoreceptors identified by magnetic screening

av 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.
I publikationen Proc Natl Acad Sci U S A (2015)

Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability

av Breuss, Martin W., Nguyen, Thai, Srivatsan, Anjana, Leca, Ines, Tian, Guoling, Fritz, Tanja, Hansen, Andi H., Musaev, Damir, McEvoy-Venneri, Jennifer, James, Kiely N., Rosti, Rasim O., Scott, Eric, Tan, Uner, Kolodner, Richard D., Cowan, Nicholas J., Keays, David A., Gleeson, Joseph G.
I publikationen Hum Mol Genet (2017)

De Novo Mutations in DENR Disrupt Neuronal Development and Link Congenital Neurological Disorders to Faulty mRNA Translation Re-initiation

av 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.
I publikationen Cell Rep (2016)

The biophysical, molecular, and anatomical landscape of pigeon CRY4: A candidate light-based quantal magnetosensor

av 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.
I publikationen Sci Adv (2020)

Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans

av Keays, David A., Tian, Guoling, Poirier, Karine, Huang, Guo-Jen, Siebold, Christian, Cleak, James, Oliver, Peter L., Fray, Martin, Harvey, Robert J., Molnár, Zoltán, Piñon, Maria C., Dear, Neil, Valdar, William, Brown, Steve D.M., Davies, Kay E., Rawlins, J. Nicholas P., Cowan, Nicholas J., Nolan, Patrick, Chelly, Jamel, Flint, Jonathan
Publicerad 2007

Mutations in PGAP3 Impair GPI-Anchor Maturation, Causing a Subtype of Hyperphosphatasia with Mental Retardation

av 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.
Publicerad 2014