Pages that link to "Q28509068"
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The following pages link to Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval (Q28509068):
Displaying 50 items.
- Frizzled class receptor 9 (Q21981591) (← links)
- Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice (Q24602261) (← links)
- Frizzled Receptors in Development and Disease (Q28071320) (← links)
- A human neurodevelopmental model for Williams syndrome (Q28119037) (← links)
- Smad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formation (Q28509903) (← links)
- Loss of Wnt8b has no overt effect on hippocampus development but leads to altered Wnt gene expression levels in dorsomedial telencephalon (Q28512461) (← links)
- The p53 transcriptional target gene wnt7b contributes to NGF-inducible neurite outgrowth in neuronal PC12 cells (Q28573510) (← links)
- Control of bone formation by the serpentine receptor Frizzled-9 (Q28587080) (← links)
- Frizzled-9 impairs acetylcholine receptor clustering in skeletal muscle cells (Q29347259) (← links)
- Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome (Q30736046) (← links)
- Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour (Q31043640) (← links)
- Neurodevelopmental and behavioral issues in Williams syndrome (Q31107088) (← links)
- Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior (Q31143422) (← links)
- Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice (Q33905573) (← links)
- Wnt2 expression and signaling is increased by different classes of antidepressant treatments (Q34088354) (← links)
- Early natural stimulation through environmental enrichment accelerates neuronal development in the mouse dentate gyrus (Q34147681) (← links)
- Altered microstructure within social-cognitive brain networks during childhood in Williams syndrome (Q34396199) (← links)
- Williams syndrome as a model for elucidation of the pathway genes - the brain - cognitive functions: genetics and epigenetics (Q34417419) (← links)
- Frizzled-8 receptor is activated by the Wnt-2 ligand in non-small cell lung cancer. (Q34788226) (← links)
- Neuropsychological components of intellectual disability: the contributions of immediate, working, and associative memory (Q34939918) (← links)
- Talampanel suppresses the acute and chronic effects of seizures in a rodent neonatal seizure model (Q34946029) (← links)
- Epigenetic regulation of neuronal dendrite and dendritic spine development (Q35018423) (← links)
- Ubiquitin ligase HUWE1 regulates axon branching through the Wnt/β-catenin pathway in a Drosophila model for intellectual disability (Q35058663) (← links)
- Alterations in diffusion properties of white matter in Williams syndrome (Q35421520) (← links)
- Can we safely target the WNT pathway? (Q35591995) (← links)
- WNTs in synapse formation and neuronal circuitry (Q36049572) (← links)
- Sudden death in toddlers associated with developmental abnormalities of the hippocampus: a report of five cases (Q36834310) (← links)
- Genetic regulation of dentate gyrus morphogenesis (Q36926802) (← links)
- A role for WNT/β-catenin signaling in the neural mechanisms of behavior (Q37109722) (← links)
- Failure of neuronal homeostasis results in common neuropsychiatric phenotypes (Q37228150) (← links)
- Generation of Frizzled10-Cre transgenic mouse line: a useful tool for the study of dorsal telencephalic development (Q37304826) (← links)
- Wnt signaling in development and disease (Q37600117) (← links)
- WNT/Frizzled signalling: receptor-ligand selectivity with focus on FZD-G protein signalling and its physiological relevance: IUPHAR Review 3 (Q37635264) (← links)
- Animal models of Williams syndrome (Q37738826) (← links)
- International Union of Basic and Clinical Pharmacology. LXXX. The Class Frizzled Receptors (Q37809668) (← links)
- Wnt signaling during synaptic development and plasticity (Q37829071) (← links)
- A review of the evidence for the canonical Wnt pathway in autism spectrum disorders (Q38053503) (← links)
- Hippocampal Wnt Signaling: Memory Regulation and Hormone Interactions. (Q38365364) (← links)
- Canonical and noncanonical Wnt signaling in neural stem/progenitor cells. (Q38573790) (← links)
- Wnt-5a/Frizzled9 Receptor Signaling through the Gαo-Gβγ Complex Regulates Dendritic Spine Formation (Q38758699) (← links)
- Wnt/β-catenin signaling plays an ever-expanding role in stem cell self-renewal, tumorigenesis and cancer chemoresistance. (Q38807957) (← links)
- Modeling Williams syndrome with induced pluripotent stem cells (Q38947225) (← links)
- Role of G Protein-Coupled Receptors in the Regulation of Structural Plasticity and Cognitive Function (Q39454293) (← links)
- Trans-synaptic transmission of vesicular Wnt signals through Evi/Wntless (Q39753324) (← links)
- Dynamic temporal and cell type-specific expression of Wnt signaling components in the developing midbrain (Q40309993) (← links)
- More than the sum of its parts: new mouse models for dissecting the genetic complexities of Williams-Beuren syndrome (Q42029377) (← links)
- The role of Wnt signaling in neuronal dysfunction in Alzheimer's Disease (Q42390629) (← links)
- Analyses of mental dysfunction-related ACSl4 in Drosophila reveal its requirement for Dpp/BMP production and visual wiring in the brain (Q43614539) (← links)
- Role of Wnt1 and Fzd1 in the spinal cord pathogenesis of amyotrophic lateral sclerosis-transgenic mice (Q43878437) (← links)
- C4ORF48, a gene from the Wolf-Hirschhorn syndrome critical region, encodes a putative neuropeptide and is expressed during neocortex and cerebellar development (Q43932025) (← links)