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Robin Reed

Affiliations: 
Cell Biology Harvard Medical School, Boston, MA, United States 
Area:
mRNA nuclear export, splicing
Website:
http://reed.med.harvard.edu/
Google:
"Robin Reed"
Mean distance: 14.83 (cluster 11)
 		SNBCP
Cross-listing: Neurotree - Cell Biology Tree

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Parents

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Tom Maniatis grad student Harvard

Children

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Zhaolan (Joe) Zhou grad student Harvard Medical School (Neurotree)
Katrin F. Chua grad student 2001 Harvard (Neurotree)
Jeanne L. Hsu grad student 2008 Harvard (Neurotree)
Patricia Valencia grad student 2008 Harvard (Neurotree)
Kobina N. Dufu grad student 2010 Harvard (Neurotree)
Hong Cheng post-doc Harvard Medical School
Seiji Masuda post-doc Harvard Medical School

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Publications

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Wang K, Yin C, Du X, et al. (2019) A U2-snRNP-independent role of SF3b in promoting mRNA export. Proceedings of the National Academy of Sciences of the United States of America
Chi B, O'Connell JD, Iocolano AD, et al. (2018) The neurodegenerative diseases ALS and SMA are linked at the molecular level via the ASC-1 complex. Nucleic Acids Research
Yin S, Iocolano A, Yu Y, et al. (2018) In Vitro System for Coupling RNAP II Transcription to Primary microRNA Processing and a Three-Way System for RNAP II Transcription/Splicing/microRNA Processing. Methods in Molecular Biology (Clifton, N.J.). 1823: 43-50
Chi B, O'Connell JD, Yamazaki T, et al. (2018) Interactome analyses revealed that the U1 snRNP machinery overlaps extensively with the RNAP II machinery and contains multiple ALS/SMA-causative proteins. Scientific Reports. 8: 8755
Yin S, Lopez-Gonzalez R, Kunz RC, et al. (2017) Evidence that C9ORF72 Dipeptide Repeat Proteins Associate with U2 snRNP to Cause Mis-splicing in ALS/FTD Patients. Cell Reports. 19: 2244-2256
Wang L, Brooks AN, Fan J, et al. (2016) Transcriptomic Characterization of SF3B1 Mutation Reveals Its Pleiotropic Effects in Chronic Lymphocytic Leukemia. Cancer Cell
Shi M, Zhang H, Wang L, et al. (2015) Premature Termination Codons Are Recognized in the Nucleus in A Reading-Frame Dependent Manner. Cell Discovery. 1
Kumar R, Corbett MA, van Bon BW, et al. (2015) THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability. American Journal of Human Genetics
Yu Y, Reed R. (2015) FUS functions in coupling transcription to splicing by mediating an interaction between RNAP II and U1 snRNP. Proceedings of the National Academy of Sciences of the United States of America
Yu Y, Chi B, Xia W, et al. (2015) U1 snRNP is mislocalized in ALS patient fibroblasts bearing NLS mutations in FUS and is required for motor neuron outgrowth in zebrafish. Nucleic Acids Research. 43: 3208-18
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