Ranjan Batra

发表

HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy

M. Swanson, M. Scotti, Wei Xie, 2020, Proceedings of the National Academy of Sciences.

Muscleblind-like 2-Mediated Alternative Splicing in the Developing Brain and Dysregulation in Myotonic Dystrophy

M. Ares, R. Darnell, M. Cline, 2012, Neuron.

Developments in RNA splicing and disease.

Michael G. Poulos, M. Swanson, R. Batra, 2011, Cold Spring Harbor perspectives in biology.

Protein-RNA Networks Regulated by Normal and ALS-Associated Mutant HNRNPA2B1 in the Nervous System

Christopher B. Burge, Steven Finkbeiner, Gene W. Yeo, 2016, Neuron.

Global insights into alternative polyadenylation regulation

M. Swanson, R. Batra, Mini Manchanda, 2015, RNA biology.

Loss of MBNL leads to disruption of developmentally regulated alternative polyadenylation in RNA-mediated disease.

Chaolin Zhang, M. Swanson, K. Sobczak, 2014, Molecular cell.

Mouse Models of C9orf72 Hexanucleotide Repeat Expansion in Amyotrophic Lateral Sclerosis/ Frontotemporal Dementia

Chris W. Lee, R. Batra, Ranjan Batra, 2017, Front. Cell. Neurosci..

Distinct and shared functions of ALS-associated proteins TDP-43, FUS and TAF15 revealed by multisystem analyses

Gene W. Yeo, C. Burge, T. Liang, 2016, Nature Communications.

Aberrant NOVA1 function disrupts alternative splicing in early stages of amyotrophic lateral sclerosis

Gene W. Yeo, J. Winkler, K. Boldt, 2022, Acta Neuropathologica.

Properties of LINE-1 proteins and repeat element expression in the context of amyotrophic lateral sclerosis

D. Trono, H. Kazazian, J. Mayer, 2018, Mobile DNA.

Elimination of Toxic Microsatellite Repeat Expansion RNA by RNA-Targeting Cas9

Gene W. Yeo, Maurice S. Swanson, Stefan Aigner, 2017, Cell.

Partners in crime: bidirectional transcription in unstable microsatellite disease.

M. Swanson, R. Batra, K. Charizanis, 2010, Human molecular genetics.

Distinct brain transcriptome profiles in C9orf72-associated and sporadic ALS

Christian A. Ross, Kevin F. Bieniek, Hu Li, 2015, Nature Neuroscience.

RNA binding protein CPEB1 remodels host and viral RNA landscapes

Gene W. Yeo, M. Ares, C. Gelboin-Burkhart, 2016, Nature Structural &Molecular Biology.

The sustained expression of Cas9 targeting toxic RNAs reverses disease phenotypes in mouse models of myotonic dystrophy type 1

Gene W. Yeo, M. Swanson, S. Blue, 2020, Nature Biomedical Engineering.

Elimination of ToxicMicrosatellite Repeat Expansion RNA by RNA-Targeting Cas 9 Graphical

Gene W. Yeo, M. Swanson, S. Blue, 2017 .

Reversal of molecular pathology by RNA-targeting Cas9 in a myotonic dystrophy mouse model

Gene W. Yeo, M. Swanson, S. Blue, 2017, bioRxiv.

Title : Reversal of molecular pathology by RNA-targeting Cas 9 in a myotonic dystrophy mouse model

Gene W. Yeo, M. Swanson, S. Blue, 2017 .

RNA-binding proteins in neurodegeneration: Seq and you shall receive

Gene W. Yeo, Clotilde Lagier-Tourenne, C. Lagier-Tourenne, 2015, Trends in Neurosciences.

Compound loss of muscleblind-like function in myotonic dystrophy

M. Swanson, L. Ranum, Christopher M. Chamberlain, 2013, EMBO molecular medicine.

MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain.

Sebastien M. Weyn-Vanhentenryck, L. Buée, Chaolin Zhang, 2015, Cell reports.

Protein-RNA Networks Re gulated by Normal and ALS-Associated Mutant HNRNPA 2 B 1 in the Nervous System Highlights

Gene W. Yeo, M. Ares, C. Burge, 2016 .

Title Distinct and shared functions of ALS-associated proteins TDP-43 , FUS and TAF 15 revealed by multisystem analyses Permalink

T. Liang, Nicole J. Lambert, Peter Freese, 2016 .

Transcriptome–pathology correlation identifies interplay between TDP-43 and the expression of its kinase CK1E in sporadic ALS

Gene W. Yeo, B. Winner, Z. Kohl, 2018, Acta Neuropathologica.