G
Glenn C. Federe
Researcher at Genomics Institute of the Novartis Research Foundation
Publications - 6
Citations - 607
Glenn C. Federe is an academic researcher from Genomics Institute of the Novartis Research Foundation. The author has contributed to research in topics: Cas9 & Genome. The author has an hindex of 5, co-authored 6 publications receiving 484 citations.
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Journal ArticleDOI
Proteasome inhibition for treatment of leishmaniasis, Chagas disease and sleeping sickness
Shilpi Khare,Advait Nagle,Agnes Biggart,Yin H. Lai,Fang Liang,Lauren C. Davis,S. Whitney Barnes,Casey J. N. Mathison,Elmarie Myburgh,Elmarie Myburgh,Mu-Yun Gao,J. Robert Gillespie,Xianzhong Liu,Jocelyn Tan,Monique Stinson,Ianne C. Rivera,Jaime Ballard,Vince Yeh,Todd Groessl,Glenn C. Federe,Hazel X. Y. Koh,John D. Venable,Badry Bursulaya,Michael Shapiro,Pranab Mishra,Glen Spraggon,Ansgar Brock,Jeremy C. Mottram,Jeremy C. Mottram,Frederick S. Buckner,Srinivasa P. S. Rao,Ben G. Wen,John R. Walker,Tove Tuntland,Valentina Molteni,Richard Glynne,Frantisek Supek +36 more
TL;DR: A selective inhibitor of the kinetoplastid proteasome (GNF6702) with unprecedented in vivo efficacy, which cleared parasites from mice in all three models of infection, underscores the possibility of developing a single class of drugs for these neglected diseases.
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Whole-genome sequencing and microarray analysis of ex vivo Plasmodium vivax reveal selective pressure on putative drug resistance genes
Neekesh V. Dharia,A. Taylor Bright,Scott J. Westenberger,S. Whitney Barnes,Serge Batalov,Kelli Kuhen,Rachel Borboa,Glenn C. Federe,Colleen M. McClean,Joseph M. Vinetz,Victor Neyra,Alejandro Llanos-Cuentas,John W. Barnwell,John R. Walker,Elizabeth A. Winzeler +14 more
TL;DR: It is shown here that whole-genome analysis of the parasite can be achieved directly from ex vivo-isolated parasites, without the need for in vitro propagation, and provides a data set for comparative analysis with important potential for identifying markers for global parasite diversity and drug resistance mapping studies.
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Efficacy and immunogenicity of Mycobacterium bovis ΔRD1 against aerosol M. bovis infection in neonatal calves
W. Ray Waters,Mitchell V. Palmer,Brian J. Nonnecke,Tyler C. Thacker,Charles F. Capinos Scherer,D. Mark Estes,R. Glyn Hewinson,H. Martin Vordermeier,S. Whitney Barnes,Glenn C. Federe,John R. Walker,Richard Glynne,Tsungda Hsu,Brian Weinrick,Karolin Biermann,Michelle H. Larsen,William R. Jacobs +16 more
TL;DR: An attenuated Mycobacterium bovisRD1 deletion (DeltaRD1) mutant of the Ravenel strain was constructed, characterized, and sequenced and may prove useful for bovine TB vaccine programs, particularly if additional mutations are included to improve safety and immunogenicity.
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Guide Swap enables genome-scale pooled CRISPR-Cas9 screening in human primary cells.
Pamela Y. Ting,Pamela Y. Ting,Albert E. Parker,Albert E. Parker,J. Scott Lee,Chris Trussell,Orzala Sharif,Fabio Luna,Glenn C. Federe,S. Whitney Barnes,John R. Walker,Julie Vance,Mu-Yun Gao,Heath E. Klock,Heath E. Klock,Scott Clarkson,Carsten Russ,Loren Miraglia,Michael P. Cooke,Anthony E. Boitano,Peter McNamara,John Lamb,Christian Schmedt,Jennifer Snead +23 more
TL;DR: Guide Swap permits genome-scale pooled CRISPR–Cas9 screening in human primary cells by exploiting the unexpected finding that editing by lentivirally delivered, targeted guide RNAs (gRNAs) occurs efficiently when Cas9 is introduced in complex with nontargeting gRNA.
Journal ArticleDOI
Tropifexor-Mediated Abrogation of Steatohepatitis and Fibrosis Is Associated With the Antioxidative Gene Expression Profile in Rodents.
Eloy D. Hernandez,Lianxing Zheng,Young Kim,Bin Fang,Bo Liu,Reginald Valdez,Reginald Valdez,William F. Dietrich,Paul Vincent Rucker,Chianelli Donatella,James Schmeits,Dingjiu Bao,Jocelyn Zoll,Claire Dubois,Glenn C. Federe,Lihao Chen,Sean B. Joseph,Lloyd B. Klickstein,John R. Walker,Valentina Molteni,Peter McNamara,Shelly Meeusen,David C. Tully,Michael Badman,Jie Xu,Bryan Laffitte +25 more
TL;DR: E efficacy of the novel nonbile acid FXR agonist tropifexor (LJN452) in two distinct preclinical models of NASH was superior to that of OCA at 25 mg/kg in the liver in both NASH models.