Pages that link to "Q33790169"
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The following pages link to Molecular Genetics of Neuronal Migration Disorders (Q33790169):
Displaying 50 items.
- Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth (Q24338872) (← links)
- Genes and brain malformations associated with abnormal neuron positioning (Q26779045) (← links)
- Molecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disorders (Q26853035) (← links)
- Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development (Q28081179) (← links)
- Phospho-NHE3 forms membrane patches and interacts with beta-actin to sense and maintain constant direction during cell migration (Q28581438) (← links)
- Doublecortin (DCX) mediates endocytosis of neurofascin independently of microtubule binding (Q30273658) (← links)
- Different Doublecortin (DCX) Patient Alleles Show Distinct Phenotypes in Cultured Neurons: EVIDENCE FOR DIVERGENT LOSS-OF-FUNCTION AND "OFF-PATHWAY" CELLULAR MECHANISMS. (Q30275553) (← links)
- Ctip2-, Satb2-, Prox1-, and GAD65-Expressing Neurons in Rat Cultures: Preponderance of Single- and Double-Positive Cells, and Cell Type-Specific Expression of Neuron-Specific Gene Family Members, Nsg-1 (NEEP21) and Nsg-2 (P19) (Q30278528) (← links)
- Adapting for endocytosis: roles for endocytic sorting adaptors in directing neural development (Q30300136) (← links)
- Heterozygous Disruption of Autism susceptibility candidate 2 Causes Impaired Emotional Control and Cognitive Memory (Q30393988) (← links)
- A behavioral evaluation of sex differences in a mouse model of severe neuronal migration disorder (Q30449377) (← links)
- The genetics of reading disabilities: from phenotypes to candidate genes (Q30459192) (← links)
- Macrophage mesenchymal migration requires podosome stabilization by filamin A (Q30513877) (← links)
- A diagnostic approach for cerebral palsy in the genomic era. (Q30857266) (← links)
- Neuronal Polarity in the Embryonic Mammalian Cerebral Cortex (Q33804436) (← links)
- Transcriptional dysregulation of neocortical circuit assembly in ASD (Q33931065) (← links)
- CNS involvement in OFD1 syndrome: a clinical, molecular, and neuroimaging study (Q33960375) (← links)
- Whole-exome sequencing identifies a de novo TUBA1A mutation in a patient with sporadic malformations of cortical development: a case report (Q33988618) (← links)
- Influence of sex and genetic variability on expression of X-linked genes in human monocytes. (Q34200936) (← links)
- Human Ntera2 cells as a predictive in vitro test system for developmental neurotoxicity (Q34361985) (← links)
- Position of neocortical neurons transfected at different gestational ages with shRNA targeted against candidate dyslexia susceptibility genes (Q34750026) (← links)
- Somatic mutations in cerebral cortical malformations (Q34763259) (← links)
- In vivo clonal overexpression of neuroligin 3 and neuroligin 2 in neurons of the rat cerebral cortex: Differential effects on GABAergic synapses and neuronal migration (Q35547559) (← links)
- Increased Blood-Reelin-Levels in First Episode Schizophrenia (Q35754509) (← links)
- Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex (Q35866505) (← links)
- Differentially expressed proteins underlying childhood cortical dysplasia with epilepsy identified by iTRAQ proteomic profiling (Q36286208) (← links)
- Dicer is required for proliferation, viability, migration and differentiation in corticoneurogenesis (Q36320541) (← links)
- Kinesin-1 acts with netrin and DCC to maintain sensory neuron position in Caenorhabditis elegans (Q36784741) (← links)
- Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A. (Q36809682) (← links)
- Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment (Q37010437) (← links)
- Efficient Generation of Corticofugal Projection Neurons from Human Embryonic Stem Cells (Q37040072) (← links)
- Non-invasive neural stem cells become invasive in vitro by combined FGF2 and BMP4 signaling (Q37096486) (← links)
- N-acetylcysteine attenuates lipopolysaccharide-induced impairment in lamination of Ctip2-and Tbr1- expressing cortical neurons in the developing rat fetal brain (Q37219991) (← links)
- Emerging roles of sumoylation in the regulation of actin, microtubules, intermediate filaments, and septins (Q37308644) (← links)
- A patient with lissencephaly, developmental delay, and infantile spasms, due to de novo heterozygous mutation of KIF2A. (Q37427210) (← links)
- The Caenorhabditis elegans microtubule minus-end binding homolog PTRN-1 stabilizes synapses and neurites (Q37596039) (← links)
- Location of periventricular nodular heterotopia is related to the malformation phenotype on MRI. (Q37632709) (← links)
- Past and present definitions of epileptogenesis and its biomarkers (Q37717423) (← links)
- Neural stem cells: are they the hope of a better life for patients with fetal-onset hydrocephalus? (Q37727816) (← links)
- Recent advances in the genetic etiology of brain malformations (Q38116442) (← links)
- New innovations: therapeutic opportunities for intellectual disabilities (Q38137883) (← links)
- Cellular and molecular introduction to brain development (Q38549130) (← links)
- Rab, Arf, and Arl-Regulated Membrane Traffic in Cortical Neuron Migration (Q38640098) (← links)
- Loss of Elp3 Impairs the Acetylation and Distribution of Connexin-43 in the Developing Cerebral Cortex (Q38703396) (← links)
- An Overview of the Mechanisms of Abnormal GABAergic Interneuronal Cortical Migration Associated with Prenatal Ethanol Exposure (Q39119147) (← links)
- Peptide regulation of cofilin activity in the CNS: A novel therapeutic approach for treatment of multiple neurological disorders (Q39148389) (← links)
- Psychiatric behaviors associated with cytoskeletal defects in radial neuronal migration (Q39314105) (← links)
- Cleave but not leave: Astrotactin proteins in development and disease. (Q39314525) (← links)
- From genetics to genomics of epilepsy. (Q39611303) (← links)
- Commissural axonal corridors instruct neuronal migration in the mouse spinal cord. (Q40954377) (← links)