Pages that link to "Q33787239"
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The following pages link to Septin 14 is involved in cortical neuronal migration via interaction with Septin 4. (Q33787239):
Displaying 33 items.
- Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development (Q27320880) (← links)
- LIN7A depletion disrupts cerebral cortex development, contributing to intellectual disability in 12q21-deletion syndrome (Q28541331) (← links)
- Septins promote stress fiber-mediated maturation of focal adhesions and renal epithelial motility (Q30405644) (← links)
- Septin-driven coordination of actin and microtubule remodeling regulates the collateral branching of axons. (Q30517924) (← links)
- Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex (Q30670360) (← links)
- The step-wise pathway of septin hetero-octamer assembly in budding yeast (Q33769772) (← links)
- During tangential migration, SDF1 lends the cytoskeleton a guiding hand (Q34123777) (← links)
- The emerging functions of septins in metazoans (Q34224017) (← links)
- Transcriptome analysis of amoeboid and ramified microglia isolated from the corpus callosum of rat brain (Q34304022) (← links)
- Spatial guidance of cell asymmetry: septin GTPases show the way. (Q35633465) (← links)
- Septin functions in organ system physiology and pathology (Q35673813) (← links)
- Partial Functional Diversification of Drosophila melanogaster Septin Genes Sep2 and Sep5. (Q37079550) (← links)
- Proteome rearrangements after auditory learning: high-resolution profiling of synapse-enriched protein fractions from mouse brain. (Q37384800) (← links)
- SIL1, a causative cochaperone gene of Marinesco-Söjgren syndrome, plays an essential role in establishing the architecture of the developing cerebral cortex (Q37644393) (← links)
- Role of a circadian-relevant gene NR1D1 in brain development: possible involvement in the pathophysiology of autism spectrum disorders (Q37682094) (← links)
- Septin roles in tumorigenesis. (Q37899208) (← links)
- Application of in utero electroporation and live imaging in the analyses of neuronal migration during mouse brain development (Q37995117) (← links)
- Comparative expression analysis of Septin 14 in testes of infertile men with normal spermatogenesis and spermatogenic failure (Q39207616) (← links)
- SEPT4 is regulated by the Notch signaling pathway (Q39469997) (← links)
- SEPT9 occupies the terminal positions in septin octamers and mediates polymerization-dependent functions in abscission (Q40376256) (← links)
- A population study of binocular function. (Q41222620) (← links)
- De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features (Q41551222) (← links)
- MUNC18-1 gene abnormalities are involved in neurodevelopmental disorders through defective cortical architecture during brain development. (Q47108329) (← links)
- Septin C-terminal domain interactions: implications for filament stability and assembly (Q48035444) (← links)
- Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability (Q48455908) (← links)
- Role of an adaptor protein Lin-7B in brain development: possible involvement in autism spectrum disorders (Q48559316) (← links)
- SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain (Q48793033) (← links)
- Characterization of presynaptic septin complexes in mammalian hippocampal neurons (Q49036967) (← links)
- [Functional Characterization of Septin Complexes]. (Q55385052) (← links)
- A Rare EGFR-SEPT14 Fusion in a Patient with Colorectal Adenocarcinoma Responding to Erlotinib (Q90257574) (← links)
- Cytoskeletal makeup of the synapse: Shaft versus spine (Q91424732) (← links)
- A homozygous genome-edited Sept2-EGFP fibroblast cell line (Q92693934) (← links)
- SEPT14 Mutations and Teratozoospermia: Genetic Effects on Sperm Head Morphology and DNA Integrity (Q92876774) (← links)