Pages that link to "Q58417213"
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The following pages link to Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development (Q58417213):
Displaying 50 items.
- A meckelin-filamin A interaction mediates ciliogenesis (Q24298551) (← links)
- Genomic structure of a novel chloride channel gene, CLIC2, in Xq28 (Q24319769) (← links)
- Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22 (Q24517924) (← links)
- The integrin-actin connection, an eternal love affair (Q24676735) (← links)
- Structural and functional aspects of filamins (Q28187219) (← links)
- Filamin A-interacting protein (FILIP) regulates cortical cell migration out of the ventricular zone (Q28203585) (← links)
- Reelin deficiency and displacement of mature neurons, but not neurogenesis, underlie the formation of granule cell dispersion in the epileptic hippocampus (Q28236724) (← links)
- Genetic malformations of cortical development (Q28242257) (← links)
- Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein (Q28263735) (← links)
- Effect of developmental exposure to chlorpyrifos on the expression of neurotrophin growth factors and cell-specific markers in neonatal rat brain (Q28566150) (← links)
- A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A (Q28569688) (← links)
- Thyroid hormone regulates reelin and dab1 expression during brain development (Q28579030) (← links)
- Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis (Q28591363) (← links)
- Mechanical dynamics in live cells and fluorescence-based force/tension sensors (Q28834419) (← links)
- Distribution and initiation of seizure activity in a rat brain with subcortical band heterotopia (Q30305641) (← links)
- Normotopic and heterotopic cortical representations of mystacial vibrissae in rats with subcortical band heterotopia (Q30308345) (← links)
- A Genetic Animal Model of Human Neocortical Heterotopia Associated with Seizures (Q30470784) (← links)
- Heterotopic neurogenesis in a rat with cortical heterotopia. (Q30472774) (← links)
- Peritrigonal and temporo-occipital heterotopia with corpus callosum and cerebellar dysgenesis (Q30558796) (← links)
- Periventricular nodular heterotopia and childhood absence epilepsy (Q30577250) (← links)
- Clinical spectrum of cortical dysplasia in childhood: diagnosis and treatment issues (Q30585938) (← links)
- Malformations of cortical development and epilepsy (Q30635675) (← links)
- Magnetic resonance imaging: role in the understanding of cerebral malformations (Q30667222) (← links)
- Neuronal migration, cerebral cortical development, and cerebral cortical anomalies (Q30671553) (← links)
- Periventricular nodular heterotopia: report of a pediatric series (Q30700496) (← links)
- Mapping form and function in the human brain: the emerging field of functional neuroimaging in cortical malformations (Q30886913) (← links)
- Cortical malformations and epilepsy: Role of MR imaging (Q31075837) (← links)
- FLNA p.V528M substitution is neither associated with bilateral periventricular nodular heterotopia nor with macrothrombocytopenia (Q33391893) (← links)
- FlnA-null megakaryocytes prematurely release large and fragile platelets that circulate poorly (Q33395689) (← links)
- Germline mosaicism in X-linked periventricular nodular heterotopia (Q33415773) (← links)
- Periventricular heterotopia and the genetics of neuronal migration in the cerebral cortex (Q33655121) (← links)
- Genetic malformations of the human cerebral cortex (Q33685187) (← links)
- Cortical malformations and epilepsy: new insights from animal models (Q33685947) (← links)
- Neuronal migration disorders in humans and in mouse models--an overview (Q33748765) (← links)
- Recent advances in the genetics of epilepsy: insights from human and animal studies (Q33755692) (← links)
- Central nervous system malformations: locations of known human mutations (Q33793036) (← links)
- A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition (Q33808422) (← links)
- How to construct a neural tube (Q33850885) (← links)
- Neocortical malformation as consequence of nonadaptive regulation of neuronogenetic sequence (Q33971556) (← links)
- Genetics of neuronal migration in the cerebral cortex (Q33971562) (← links)
- Neuronal migration disorders: from genetic diseases to developmental mechanisms (Q33976255) (← links)
- Drosophila Ten-m and filamin affect motor neuron growth cone guidance. (Q33999066) (← links)
- Neuronal migration defects of the cerebral cortex: a destination debacle (Q34005927) (← links)
- Cortical malformations and epilepsy (Q34099221) (← links)
- Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans. (Q34180628) (← links)
- Cell migration and cerebral cortical development (Q34216765) (← links)
- Filamin A regulates focal adhesion disassembly and suppresses breast cancer cell migration and invasion (Q34243424) (← links)
- MEK-ERK1/2-dependent FLNA overexpression promotes abnormal dendritic patterning in tuberous sclerosis independent of mTOR. (Q34288834) (← links)
- X-linked malformations of cortical development (Q34306145) (← links)
- Epilepsy and brain abnormalities in mice lacking the Otx1 gene (Q34400653) (← links)