Pages that link to "Q33851469"
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The following pages link to Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects (Q33851469):
Displaying 28 items.
- Conserved roles for cytoskeletal components in determining laterality (Q27334688) (← links)
- p600 regulates spindle orientation in apical neural progenitors and contributes to neurogenesis in the developing neocortex. (Q33757246) (← links)
- A point mutation in translation initiation factor eIF2B leads to function--and time-specific changes in brain gene expression (Q34071458) (← links)
- Kinesin-12 influences axonal growth during zebrafish neural development (Q34536271) (← links)
- Transcriptomic changes in brain development (Q36325687) (← links)
- Cytoskeleton in action: lissencephaly, a neuronal migration disorder (Q36672834) (← links)
- LIS1 deficiency promotes dysfunctional synaptic integration of granule cells generated in the developing and adult dentate gyrus (Q37117356) (← links)
- Integrative mechanisms of oriented neuronal migration in the developing brain (Q37596072) (← links)
- LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules. (Q38166377) (← links)
- p600/UBR4 in the central nervous system (Q38271411) (← links)
- Regulation of neuronal migration, an emerging topic in autism spectrum disorders (Q38612196) (← links)
- Targeting protein for xenopus kinesin-like protein 2 (TPX2) regulates γ-histone 2AX (γ-H2AX) levels upon ionizing radiation (Q39263901) (← links)
- Identification of novel radiation-induced p53-dependent transcripts extensively regulated during mouse brain development (Q41436986) (← links)
- fosB-null mice display impaired adult hippocampal neurogenesis and spontaneous epilepsy with depressive behavior (Q41495316) (← links)
- Cell cycle networks link gene expression dysregulation, mutation, and brain maldevelopment in autistic toddlers (Q41869289) (← links)
- 14-3-3 Proteins in Brain Development: Neurogenesis, Neuronal Migration and Neuromorphogenesis (Q42694677) (← links)
- Transcriptome analysis reveals rod/cone photoreceptor specific signatures across mammalian retinas (Q46421739) (← links)
- Genetic associations with reflexive visual attention in infancy and childhood (Q48097226) (← links)
- Early born neurons are abnormally positioned in the doublecortin knockout hippocampus (Q48385619) (← links)
- Developmental dynamics of PAFAH1B subunits during mouse brain development (Q48556279) (← links)
- Tau's role in the developing brain: implications for intellectual disability (Q48756991) (← links)
- CHCHD2 is down-regulated in neuronal cells differentiated from iPS cells derived from patients with lissencephaly. (Q52151878) (← links)
- Neurodevelopmental Genetic Diseases Associated With Microdeletions and Microduplications of Chromosome 17p13.3. (Q52431395) (← links)
- Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girl. (Q53151683) (← links)
- CRISPR/Cas9-mediated kif15 mutations accelerate axonal outgrowth during neuronal development and regeneration in zebrafish (Q58590795) (← links)
- C2H2-Type Zinc Finger Proteins in Brain Development, Neurodevelopmental, and Other Neuropsychiatric Disorders: Systematic Literature-Based Analysis (Q89964981) (← links)
- Nervous NDRGs: the N-myc downstream-regulated gene family in the central and peripheral nervous system (Q93111949) (← links)
- Postnatal Role of the Cytoskeleton in Adult Epileptogenesis (Q99631302) (← links)