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The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

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Results: 11 to 20 of 21

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Genome-wide screen reveals APC-associated RNAs enriched in cell protrusions.
Mili S, Moissoglu K, Macara IG
(2008) Nature 453: 115-9
MeSH Terms: 3' Untranslated Regions, Adenomatous Polyposis Coli Protein, Animals, Cell Movement, Cell Polarity, Fibroblasts, Fragile X Mental Retardation Protein, Genome, Genomics, Humans, Mice, Microtubules, NIH 3T3 Cells, Oligonucleotide Array Sequence Analysis, Pseudopodia, RNA, RNA Transport
Added March 5, 2014
0 Communities
1 Members
0 Resources
17 MeSH Terms
Fragile X gene premutation in multiple system atrophy.
Garland EM, Vnencak-Jones CL, Biaggioni I, Davis TL, Montine TJ, Robertson D
(2004) J Neurol Sci 227: 115-8
MeSH Terms: Aged, Aged, 80 and over, Female, Fragile X Mental Retardation Protein, Humans, Male, Middle Aged, Multiple System Atrophy, Nerve Tissue Proteins, Phenotype, RNA, Messenger, RNA-Binding Proteins, Reverse Transcriptase Polymerase Chain Reaction, Sex Factors, Trinucleotide Repeat Expansion
Added December 10, 2013
0 Communities
2 Members
0 Resources
15 MeSH Terms
Prevalence of the fragile X syndrome in African-Americans.
Crawford DC, Meadows KL, Newman JL, Taft LF, Scott E, Leslie M, Shubek L, Holmgreen P, Yeargin-Allsopp M, Boyle C, Sherman SL
(2002) Am J Med Genet 110: 226-33
MeSH Terms: Alleles, Blacks, Child, Female, Fragile X Mental Retardation Protein, Fragile X Syndrome, Gene Frequency, Humans, Male, Mutation, Nerve Tissue Proteins, Prevalence, RNA-Binding Proteins, Trinucleotide Repeats, United States
Added December 10, 2013
0 Communities
1 Members
0 Resources
15 MeSH Terms
Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range.
Sullivan AK, Crawford DC, Scott EH, Leslie ML, Sherman SL
(2002) Am J Hum Genet 70: 1532-44
MeSH Terms: Alleles, Blacks, Fathers, Female, Fragile X Mental Retardation Protein, Fragile X Syndrome, Haplotypes, Humans, Intellectual Disability, Logistic Models, Male, Mothers, Mutagenesis, Nerve Tissue Proteins, RNA-Binding Proteins, Risk Factors, Trinucleotide Repeat Expansion, Whites
Added December 10, 2013
0 Communities
1 Members
0 Resources
18 MeSH Terms
FMR1 and the fragile X syndrome: human genome epidemiology review.
Crawford DC, Acuña JM, Sherman SL
(2001) Genet Med 3: 359-71
MeSH Terms: Female, Fragile X Mental Retardation Protein, Fragile X Syndrome, Gene Frequency, Genetic Testing, Genome, Human, Heterozygote, Humans, Male, Mutation, Nerve Tissue Proteins, RNA-Binding Proteins, Trinucleotide Repeats, Whites
Added December 10, 2013
0 Communities
1 Members
0 Resources
14 MeSH Terms
Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability.
Crawford DC, Zhang F, Wilson B, Warren ST, Sherman SL
(2000) Hum Mol Genet 9: 1759-69
MeSH Terms: 5' Untranslated Regions, African Americans, Alleles, Blacks, Female, Fragile X Mental Retardation Protein, Fragile X Syndrome, Genetic Markers, Humans, Male, Nerve Tissue Proteins, Pedigree, RNA Stability, RNA-Binding Proteins, Terminal Repeat Sequences, Trinucleotide Repeats
Added December 10, 2013
0 Communities
1 Members
0 Resources
16 MeSH Terms
Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function.
Paradee W, Melikian HE, Rasmussen DL, Kenneson A, Conn PJ, Warren ST
(1999) Neuroscience 94: 185-92
MeSH Terms: Amygdala, Animals, Conditioning, Psychological, Electrophysiology, Fear, Female, Fragile X Mental Retardation Protein, Fragile X Syndrome, Genotype, Hippocampus, Long-Term Potentiation, Male, Maze Learning, Mice, Mice, Inbred C57BL, Mice, Knockout, Nerve Tissue Proteins, Phenotype, RNA-Binding Proteins, Spatial Behavior
Added February 19, 2015
0 Communities
1 Members
0 Resources
20 MeSH Terms
Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.
Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST
(1998) Hum Mol Genet 7: 1935-46
MeSH Terms: Adenine Nucleotides, Alleles, Animals, Fragile X Mental Retardation Protein, Fragile X Syndrome, Gene Frequency, Genetic Markers, Guanine Nucleotides, Haplotypes, Humans, Introns, Linkage Disequilibrium, Male, Microsatellite Repeats, Nerve Tissue Proteins, Pan troglodytes, Polymorphism, Genetic, Polymorphism, Single-Stranded Conformational, RNA-Binding Proteins, Trinucleotide Repeats
Added December 10, 2013
0 Communities
1 Members
0 Resources
20 MeSH Terms
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.
Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M
(1993) Nat Genet 3: 36-43
MeSH Terms: Adult, Animals, Base Sequence, Blotting, Northern, Brain, DNA, Single-Stranded, Fetus, Fragile X Mental Retardation Protein, Fragile X Syndrome, Gene Expression, Humans, In Situ Hybridization, Male, Mice, Molecular Sequence Data, Nerve Tissue Proteins, Organ Specificity, RNA-Binding Proteins, Testis
Added February 20, 2014
0 Communities
1 Members
0 Resources
19 MeSH Terms
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome.
Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP
(1991) Cell 65: 905-14
MeSH Terms: Alleles, Amino Acid Sequence, Base Sequence, Blotting, Northern, Brain, Cosmids, DNA, Exons, Fragile X Mental Retardation Protein, Fragile X Syndrome, Gene Library, Gene Rearrangement, Genetic Variation, Humans, Molecular Sequence Data, Nerve Tissue Proteins, Oligonucleotide Probes, Polymerase Chain Reaction, RNA, RNA-Binding Proteins, Recombination, Genetic, Repetitive Sequences, Nucleic Acid, Restriction Mapping, Translocation, Genetic, X Chromosome
Added February 20, 2014
0 Communities
1 Members
0 Resources
25 MeSH Terms