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SMN deficiency in severe models of spinal muscular atrophy causes widespread intron retention and DNA damage. [electronic resource] by
- Jangi, Mohini
- Fleet, Christina
- Cullen, Patrick
- Gupta, Shipra V
- Mekhoubad, Shila
- Chiao, Eric
- Allaire, Norm
- Bennett, C Frank
- Rigo, Frank
- Krainer, Adrian R
- Hurt, Jessica A
- Carulli, John P
- Staropoli, John F
Producer: 20180522
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 114
Availability: No items available.
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Genetic and acute CPEB1 depletion ameliorate fragile X pathophysiology. [electronic resource] by
- Udagawa, Tsuyoshi
- Farny, Natalie G
- Jakovcevski, Mira
- Kaphzan, Hanoch
- Alarcon, Juan Marcos
- Anilkumar, Shobha
- Ivshina, Maria
- Hurt, Jessica A
- Nagaoka, Kentaro
- Nalavadi, Vijayalaxmi C
- Lorenz, Lori J
- Bassell, Gary J
- Akbarian, Schahram
- Chattarji, Sumantra
- Klann, Eric
- Richter, Joel D
Producer: 20140123
In:
Nature medicine vol. 19
Availability: No items available.
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