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

por Keays, David A.
Publicado 2007

Is magnetogenetics the new optogenetics?

por Nimpf, Simon, Keays, David A
Publicado 2017

Cryptochrome: The magnetosensor with a sinister side?

por Landler, Lukas, Keays, David A.
Publicado 2018

Why (and how) we should publish negative data

por Nimpf, Simon, Keays, David A
Publicado 2019

Myths in magnetosensation

por Nimpf, Simon, Keays, David A.
Publicado 2022

Magnetoreception—A sense without a receptor

por Nordmann, Gregory C., Hochstoeger, Tobias, Keays, David A.
Publicado 2017

MAPping tubulin mutations

por Cushion, Thomas D., Leca, Ines, Keays, David A.
Publicado 2023

Ectopic otoconial formation in the lagena of the pigeon inner ear

por Malkemper, E. Pascal, Mason, Matthew J., Kagerbauer, Daniel, Nimpf, Simon, Keays, David A.
Publicado 2018

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

por Landler, Lukas, Nimpf, Simon, Hochstoeger, Tobias, Nordmann, Gregory C, Papadaki-Anastasopoulou, Artemis, Keays, David A
Publicado 2018

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

por Pagnamenta, Alistair T., Howard, Malcolm F., Knight, Samantha J. L., Keays, David A., Quaghebeur, Gerardine, Taylor, Jenny C., Kini, Usha
Publicado 2016

Quantum magnetic imaging of iron organelles within the pigeon cochlea

por de Gille, Robert W., McCoey, Julia M., Hall, Liam T., Tetienne, Jean-Philippe, Malkemper, E. Pascal, Keays, David A., Hollenberg, Lloyd C. L., Simpson, David A.
Publicado 2021

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

por 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
Publicado 2017

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

por 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
Publicado 2015

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

por 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.
Publicado 2018

The expression, localisation and interactome of pigeon CRY2

por 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.
Publicado 2021

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

por 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
Publicado 2012

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

por 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.
Publicado 2016

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

por 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.
Publicado 2020

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

por 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
Publicado 2007

Impaired Synaptic Plasticity and Motor Learning in Mice with a Point Mutation Implicated in Human Speech Deficits

por Groszer, Matthias, Keays, David A., Deacon, Robert M.J., de Bono, Joseph P., Prasad-Mulcare, Shweta, Gaub, Simone, Baum, Muriel G., French, Catherine A., Nicod, Jérôme, Coventry, Julie A., Enard, Wolfgang, Fray, Martin, Brown, Steve D.M., Nolan, Patrick M., Pääbo, Svante, Channon, Keith M., Costa, Rui M., Eilers, Jens, Ehret, Günter, Rawlins, J. Nicholas P., Fisher, Simon E.
Publicado 2008