bioRxiv

A comprehensive portrait of cilia and ciliopathies from a CRISPR-based screen for Hedgehog signaling.

bioRxiv

David K. Breslow, Sascha Hoogendoorn, Adam R. Kopp, David W. Morgens, Brandon K. Vu, Kyuho Han, Amy Li, Gaelen T. Hess, Michael C. Bassik, James K. Chen, Maxence V. Nachury

A comprehensive portrait of cilia and ciliopathies from a CRISPR-based screen for Hedgehog signaling.

bioRxiv

David K. Breslow,Sascha Hoogendoorn,Adam R. Kopp,David W. Morgens,Brandon K. Vu,Kyuho Han,Amy Li,Gaelen T. Hess,Michael C. Bassik,James K. Chen,Maxence V. Nachury

Widespread translational remodeling during human neuronal differentiation.

bioRxiv

John D Blair, Dirk Hockemeyer, Jennifer A Doudna, Helen S Bateup, Stephen N Floor

Widespread translational remodeling during human neuronal differentiation.

bioRxiv

John D Blair,Dirk Hockemeyer,Jennifer A Doudna,Helen S Bateup,Stephen N Floor

CRISPR-Cas9 Genome Editing In Human Cells Works Via The Fanconi Anemia Pathway.

bioRxiv

Chris D. Richardson, Katelynn R. Kazane, Sharon J. Feng, Nicholas L. Bray, Axel J. Schaefer, Stephen Floor, Jacob Corn

CRISPR-Cas9 Genome Editing In Human Cells Works Via The Fanconi Anemia Pathway.

bioRxiv

Chris D. Richardson,Katelynn R. Kazane,Sharon J. Feng,Nicholas L. Bray,Axel J. Schaefer,Stephen Floor,Jacob Corn

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families.

bioRxiv

Donna M Werling, Harrison Brand, Joon-Yong An, Matthew R Stone, Joseph T Glessner, Lingxue Zhu, Ryan L Collins, Shan Dong, Ryan M Layer, Eiriene-Chloe Markenscoff-Papadimitriou, Andrew Farrell, Grace B Schwartz, Benjamin B Currall, Jeanselle Dea, Clif Duhn, Carolyn Erdman, Michael Gilson, Robert E Handsaker, Seva Kashin, Lambertus Klei, Jeffrey D Mandell, Tomasz J Nowakowski, Yuwen Liu, Sirisha Pochareddy, Louw Smith, Michael F Walker, Harold Z Wang, Mathew J Waterman, Xin He, Arnold R Kriegstein, John L Rubenstein, Nenad Sestan, Steven A McCarroll, Ben M Neale, Hilary Coon, A. Jeremy Willsey, Joseph D Buxbaum, Mark J Daly, Matthew W State, Aaron Quinlan, Gabor T Marth, Kathryn Roeder, Bernie Devlin, Michael E Talkowski, Stephan J Sanders

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families.

bioRxiv

Donna M Werling,Harrison Brand,Joon-Yong An,Matthew R Stone,Joseph T Glessner,Lingxue Zhu,Ryan L Collins,Shan Dong,Ryan M Layer,Eiriene-Chloe Markenscoff-Papadimitriou,Andrew Farrell,Grace B Schwartz,Benjamin B Currall,Jeanselle Dea,Clif Duhn,Carolyn Erdman,Michael Gilson,Robert E Handsaker,Seva Kashin,Lambertus Klei,Jeffrey D Mandell,Tomasz J Nowakowski,Yuwen Liu,Sirisha Pochareddy,Louw Smith,Michael F Walker,Harold Z Wang,Mathew J Waterman,Xin He,Arnold R Kriegstein,John L Rubenstein,Nenad Sestan,Steven A McCarroll,Ben M Neale,Hilary Coon,A. Jeremy Willsey,Joseph D Buxbaum,Mark J Daly,Matthew W State,Aaron Quinlan,Gabor T Marth,Kathryn Roeder,Bernie Devlin,Michael E Talkowski,Stephan J Sanders

OGT binds a conserved C-terminal domain of TET1 to regulate TET1 activity and function in development.

bioRxiv

Joel Hrit,Cheng Li,Elizabeth Allene Martin,Mary Goll,Barbara Panning

Local Control of Intracellular Microtubule Dynamics by End Binding Protein 1 (EB1) Photo-Dissociation.

bioRxiv

Jeffrey van Haren,Andreas Ettinger,Hui Wang,Klaus Hahn,Torsten Wittmann

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