|Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome|
AJMH Verkerk, M Pieretti, JS Sutcliffe, YH Fu, DPA Kuhl, A Pizzuti, ...
Cell 65 (5), 905-914, 1991
|Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox|
YH Fu, DPA Kuhl, A Pizzuti, M Pieretti, JS Sutcliffe, S Richards, ...
Cell 67 (6), 1047-1058, 1991
|The mGluR theory of fragile X mental retardation|
MF Bear, KM Huber, ST Warren
Trends in neurosciences 27 (7), 370-377, 2004
|Absence of expression of the FMR-1 gene in fragile X syndrome|
M Pieretti, F Zhang, YH Fu, ST Warren, BA Oostra, CT Caskey, DL Nelson
Cell 66 (4), 817-822, 1991
|Altered synaptic plasticity in a mouse model of fragile X mental retardation|
KM Huber, SM Gallagher, ST Warren, MF Bear
Proceedings of the National Academy of Sciences 99 (11), 7746-7750, 2002
|Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome|
V Brown, P Jin, S Ceman, JC Darnell, WT O'Donnell, SA Tenenbaum, ...
Cell 107 (4), 477-487, 2001
|Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p (CCG) n|
EJ Kremer, M Pritchard, M Lynch, S Yu, K Holman, E Baker, ST Warren, ...
Science 252 (5013), 1711-1714, 1991
|Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function|
GJ Bassell, ST Warren
Neuron 60 (2), 201-214, 2008
|Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function|
JC Darnell, KB Jensen, P Jin, V Brown, ST Warren, RB Darnell
Cell 107 (4), 489-499, 2001
|Fragile X genotype characterized by an unstable region of DNA|
S Yu, M Pritchard, E Kremer, M Lynch, J Nancarrow, E Baker, K Holman, ...
Science, 1179-1181, 1991
|FMR1 protein: conserved RNP family domains and selective RNA binding|
CT Ashley, KD Wilkinson, D Reines, ST Warren
Science 262 (5133), 563-566, 1993
|DNA methylation represses FMR-1 transcription in fragile X syndrome|
JS Sutcliffe, DL Nelson, F Zhang, M Pieretti, CT Caskey, D Saxe, ...
Human molecular genetics 1 (6), 397-400, 1992
|Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway|
P Jin, DC Zarnescu, S Ceman, M Nakamoto, J Mowrey, TA Jongens, ...
Nature neuroscience 7 (2), 113-117, 2004
|Split genes and RNA splicing|
Cell 77 (6), 805-815, 1994
|A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence|
HH Chou, H Takematsu, S Diaz, J Iber, E Nickerson, KL Wright, ...
Proceedings of the National Academy of Sciences 95 (20), 11751-11756, 1998
|Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes|
Y Feng, CA Gutekunst, DE Eberhart, H Yi, ST Warren, SM Hersch
Journal of Neuroscience 17 (5), 1539-1547, 1997
|A decade of molecular studies of fragile X syndrome|
WT O'Donnell, ST Warren
Annual review of neuroscience 25 (1), 315-338, 2002
|FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association|
Y Feng, D Absher, DE Eberhart, V Brown, HE Malter, ST Warren
Molecular cell 1 (1), 109-118, 1997
|Trinucleotide repeat expansion and human disease|
CT Ashley, ST Warren
Annual review of genetics 29 (1), 703-728, 1995
|The fragile X mental retardation protein inhibits translation via interacting with mRNA|
Z Li, Y Zhang, L Ku, KD Wilkinson, ST Warren, Y Feng
Nucleic acids research 29 (11), 2276-2283, 2001