Quantitative Gait Analysis Using a Motorized Treadmill System Sensitively Detects Motor Abnormalities in Mice Expressing ATPase Defective Spastin

Por Connell, James W., Allison, Rachel, Reid, Evan
Publicado no PLoS One (2016)

Vg1RBP phosphorylation by Erk2 MAP kinase correlates with the cortical release of Vg1 mRNA during meiotic maturation of Xenopus oocytes

Por Git, Anna, Allison, Rachel, Perdiguero, Eusebio, Nebreda, Angel R., Houliston, Evelyn, Standart, Nancy
Publicado em 2009

Two distinct Staufen isoforms in Xenopus are vegetally localized during oogenesis

Por ALLISON, RACHEL, CZAPLINSKI, KEVIN, GIT, ANNA, ADEGBENRO, ELIZABETH, STENNARD, FIONA, HOULISTON, EVELYN, STANDART, NANCY
Publicado em 2004

Asymmetrical β-actin mRNA translation in growth cones mediates attractive turning to netrin-1

Por Leung, Kin-Mei, van Horck, Francisca PG, Lin, Andrew C, Allison, Rachel, Standart, Nancy, Holt, Christine E
Publicado em 2006

Activation of a microRNA response in trans reveals a new role for poly(A) in translational repression

Por Ricci, Emiliano P., Limousin, Taran, Soto-Rifo, Ricardo, Allison, Rachel, Pöyry, Tuija, Decimo, Didier, Jackson, Richard J., Ohlmann, Théophile
Publicado em 2011

An ESCRT–spastin interaction promotes fission of recycling tubules from the endosome

Por Allison, Rachel, Lumb, Jennifer H., Fassier, Coralie, Connell, James W., Ten Martin, Daniel, Seaman, Matthew N.J., Hazan, Jamilé, Reid, Evan
Publicado em 2013

BMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translation

Por Jardin, Nicolas, Giudicelli, François, Ten Martín, Daniel, Vitrac, Anaïs, De Gois, Stéphanie, Allison, Rachel, Houart, Corinne, Reid, Evan, Hazan, Jamilé, Fassier, Coralie
Publicado no Development (2018)

CSF1 receptor signaling is necessary for microglia viability, which unmasks a cell that rapidly repopulates the microglia-depleted adult brain

Por Elmore, Monica Renee Pittman, Najafi, Allison Rachel, Koike, Maya Allegra, Dagher, Nabil Nazih, Spangenberg, Elizabeth Erin, Rice, Rachel Anne, Kitazawa, Masashi, Matusow, Bernice, Nguyen, Hoa, West, Brian Lee, Green, Kim Nicholas
Publicado em 2014

Defects in ER–endosome contacts impact lysosome function in hereditary spastic paraplegia

Por Allison, Rachel, Edgar, James R., Pearson, Guy, Rizo, Tania, Newton, Timothy, Günther, Sven, Berner, Fiamma, Hague, Jennifer, Connell, James W., Winkler, Jürgen, Lippincott-Schwartz, Jennifer, Beetz, Christian, Winner, Beate, Reid, Evan
Publicado no J Cell Biol (2017)

Mechanistic basis of an epistatic interaction reducing age at onset in hereditary spastic paraplegia

Por Newton, Timothy, Allison, Rachel, Edgar, James R, Lumb, Jennifer H, Rodger, Catherine E, Manna, Paul T, Rizo, Tania, Kohl, Zacharias, Nygren, Anders O H, Arning, Larissa, Schüle, Rebecca, Depienne, Christel, Goldberg, Lisa, Frahm, Christiane, Stevanin, Giovanni, Durr, Alexandra, Schöls, Ludger, Winner, Beate, Beetz, Christian, Reid, Evan
Publicado no Brain (2018)

Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12

Por Montenegro, Gladys, Rebelo, Adriana P., Connell, James, Allison, Rachel, Babalini, Carla, D’Aloia, Michela, Montieri, Pasqua, Schüle, Rebecca, Ishiura, Hiroyuki, Price, Justin, Strickland, Alleene, Gonzalez, Michael A., Baumbach-Reardon, Lisa, Deconinck, Tine, Huang, Jia, Bernardi, Giorgio, Vance, Jeffery M., Rogers, Mark T., Tsuji, Shoji, De Jonghe, Peter, Pericak-Vance, Margaret A., Schöls, Ludger, Orlacchio, Antonio, Reid, Evan, Züchner, Stephan
Publicado em 2012