Search Constraints
Search Results
Select an image to start the slideshow
Pathogenesis of novel FMR1 mutations in fragile X syndrome
1 of 10
Ubiquitin Targeting and Differential Accumulation of Mutant Huntingtin
2 of 10
The Role of Oligodendrocyte Dysfunction in Huntington's Disease
3 of 10
Genetic Diversity in Oxytocin Receptor Sequence, Neural Expression, and Social Behavior
4 of 10
An In Vivo Model to Study the Regulation of FMRP
5 of 10
The polyadenosine RNA-binding protein dNab2 interacts with the fragile X protein homolog and regulates gene expression in Drosophila neurons
6 of 10
The RNA-binding protein, ZC3H14, is critical for control of
polyadenylation and translation, neuronal development, brain
morphology, and working memory in mice
7 of 10
Molecular, Genetics, and Biochemical Studies on Troponin I and
Tropomyosin in the Regulation of Muscle Contraction
8 of 10
LSD1 Continuously Protects the Differentiated State of Neurons
9 of 10
Mutation of the Conserved Polyadenosine RNA binding protein,
ZC3H14/dNab2, Impairs Neural Function in Drosophila
and Humans
10 of 10