Fragile X Syndrome Concept

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A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation Journal Articles
A TaqI RFLP in Xq26–qter detected by pX301b [DXS311] Journal Articles
A rapid, reliable, and inexpensive method for detection of di- and trinucleotide repeat markers and disease loci from dried blood spots Journal Articles
Abnormal neural precursor cell regulation in the early postnatal Fragile X mouse hippocampus Journal Articles
An assessment of the use of flanking DNA markers for fra(X) syndrome carrier detection and prenatal diagnosis Journal Articles
Astrocyte-mediated disruption of ROS homeostasis in Fragile X mouse model Journal Articles
Astrocyte-secreted thrombospondin-1 modulates synapse and spine defects in the fragile X mouse model Journal Articles
Astrocytes Prevent Abnormal Neuronal Development in the Fragile X Mouse Journal Articles
Astrocytes and Developmental Plasticity in Fragile X Journal Articles
Astrocyte‐mediated purinergic signaling is upregulated in a mouse model of Fragile X syndrome Journal Articles
Autism Spectrum Disorders and Epigenetics Journal Articles
Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array Journal Articles
Converging purinergic and immune signaling pathways drive IL-6 secretion by Fragile X cortical astrocytes via STAT3 Journal Articles
Cranial and hand skeleton in fragile X syndrome Journal Articles
Developmental expression of FMRP in the astrocyte lineage: Implications for fragile X syndrome Journal Articles
Developmental expression of the neuroligins and neurexins in fragile X mice Journal Articles
Dysregulated Purinergic Signalling in Fragile X Syndrome Cortical Astrocytes. Journal Articles
Fragile X astrocytes induce developmental delays in dendrite maturation and synaptic protein expression Journal Articles
Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3. Journal Articles
Glial-mediated dysregulation of neurodevelopment in Fragile X Syndrome Chapters
HELP for behaviours that challenge in adults with intellectual and developmental disabilities. Journal Articles
Hippocampal neuronal subtypes develop abnormal dendritic arbors in the presence of Fragile X astrocytes Journal Articles
Isolation and mapping of a polymorphic DNA sequence, DXS312, to Xq27–Xq28 Journal Articles
Mitochondrial bioenergetics of astrocytes in Fragile X syndrome: new perspectives on culture conditions and sex effects Journal Articles
P2X7 expression patterns in the developing Fmr1-knockout mouse hippocampus. Journal Articles
Possible Similarities Between the Fragile X and Asperger's Syndromes Journal Articles
Prenatal diagnosis of fragile X syndrome: Management of the male fetus with a premutation Journal Articles
Probing Astrocyte Function in Fragile X Syndrome Journal Articles
Purinergic Signalling Mediates Aberrant Excitability of Developing Neuronal Circuits in the Fmr1 Knockout Mouse Model Journal Articles
Recombination between the factor VIII gene and the DXS52 locus gives the most probable genetic order as centromere‐FRA(X)‐DXS15‐DXS52‐F8C‐telomere Journal Articles
Regional brain volumes changes in adult male FMR1-KO mouse on the FVB strain Journal Articles
Sex Identification of Elk (Cervus elaphus canadensis), Moose (Alces alces), and White-Tailed Deer (Odocoileus virginianus) Using the Polymerase Chain Reaction Journal Articles
Sex and genes, part 2: A biopsychosocial approach to assess and treat challenging sexual behavior in persons with intellectual disabilities including fragile X syndrome and 22q11.2 deletion syndrome Journal Articles
Social Cognition in Adolescent Girls With Fragile X Syndrome Journal Articles
Specific EEG resting state biomarkers in FXS and ASD. Journal Articles
Temporal and spectral differences in the ultrasonic vocalizations of fragile X knock out mice during postnatal development Journal Articles
The Genetic Distance between the Coagulation Factor IX Gene and the Locus for the Fragile X Syndrome: Clinical Implications Journal Articles
The fragile‐X syndrome, IV. Progress towards the identification of linked restriction fragment length variants (RFLVs) Journal Articles