Pages that link to "Q24336051"
Jump to navigation
Jump to search
The following pages link to Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome (Q24336051):
Displaying 50 items.
- Platelet activating factor acetylhydrolase 1b regulatory subunit 1 (Q1982330) (← links)
- DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX) (Q22008801) (← links)
- Genomic structure, chromosomal mapping, and expression pattern of human DCAMKL1 (KIAA0369), a homologue of DCX (XLIS) (Q22008834) (← links)
- Hippocampal abnormalities and enhanced excitability in a murine model of human lissencephaly (Q22253373) (← links)
- A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function (Q24290458) (← links)
- LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome (Q24290783) (← links)
- A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome (Q24314944) (← links)
- The human ROX gene: genomic structure and mutation analysis in human breast tumors (Q24318677) (← links)
- Ndel1 palmitoylation: a new mean to regulate cytoplasmic dynein activity. (Q24318793) (← links)
- Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3 (Q24532106) (← links)
- Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit. (Q24532866) (← links)
- Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human region (Q24628667) (← links)
- Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE (Q26690426) (← links)
- DISC1: a key lead in studying cortical development and associated brain disorders (Q26851318) (← links)
- Cross-Species Integrative Functional Genomics in GeneWeaver Reveals a Role for Pafah1b1 in Altered Response to Alcohol. (Q27321572) (← links)
- Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain development (Q28139341) (← links)
- A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system (Q28143518) (← links)
- 14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome (Q28178021) (← links)
- Genetic malformations of cortical development (Q28242257) (← links)
- Variants in CUL4B are associated with cerebral malformations (Q28251358) (← links)
- The DISC locus in psychiatric illness (Q28251868) (← links)
- The lissencephaly gene product Lis1, a protein involved in neuronal migration, interacts with a nuclear movement protein, NudC (Q28271880) (← links)
- Lis1 controls dynamics of neuronal filopodia and spines to impact synaptogenesis and social behaviour (Q28509621) (← links)
- Regulation of microtubule dynamics and myogenic differentiation by MURF, a striated muscle RING-finger protein (Q28513866) (← links)
- Regulation of cytoplasmic dynein behaviour and microtubule organization by mammalian Lis1 (Q28565028) (← links)
- LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages (Q28574389) (← links)
- Inactivation of a testis-specific Lis1 transcript in mice prevents spermatid differentiation and causes male infertility (Q28589208) (← links)
- Multiple dose-dependent effects of Lis1 on cerebral cortical development (Q28589891) (← links)
- NudE-L, a novel Lis1-interacting protein, belongs to a family of vertebrate coiled-coil proteins (Q28590012) (← links)
- Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality (Q28592982) (← links)
- Human iPSC-Derived Cerebral Organoids Model Cellular Features of Lissencephaly and Reveal Prolonged Mitosis of Outer Radial Glia (Q28595116) (← links)
- Roles of NUDE and NUDF proteins of Aspergillus nidulans: insights from intracellular localization and overexpression effects (Q30477649) (← links)
- Advanced microscopic imaging methods to investigate cortical development and the etiology of mental retardation (Q30487112) (← links)
- Distinct dose-dependent cortical neuronal migration and neurite extension defects in Lis1 and Ndel1 mutant mice (Q30493243) (← links)
- Novel embryonic neuronal migration and proliferation defects in Dcx mutant mice are exacerbated by Lis1 reduction (Q30494259) (← links)
- Brain development and the genetics of brain development (Q30773677) (← links)
- The genetics of lissencephaly (Q30826834) (← links)
- Characterization and chromosomal mapping of two pseudogenes of the mouse Pafaha/Lis1 gene: retrointegration hotspots in the mouse genome (Q32026644) (← links)
- Neuroprotection and enhancement of neurite outgrowth with small molecular weight compounds from screens of chemical libraries (Q33267049) (← links)
- Isolation of BAC clones spanning the Xq22.3 translocation breakpoint in a lissencephaly patient with a de novo X;2 translocation (Q33681389) (← links)
- Genetic malformations of the human cerebral cortex (Q33685187) (← links)
- miR-139-5p modulates cortical neuronal migration by targeting Lis1 in a rat model of focal cortical dysplasia (Q33748429) (← links)
- Genes that regulate neuronal migration in the cerebral cortex (Q33748771) (← links)
- Preferential Association of Lissencephaly-1 Gene Expression with CD133 Glioblastoma Cells. (Q33776755) (← links)
- Molecular mechanisms for CMT1A duplication and HNPP deletion (Q33787286) (← links)
- Molecular Genetics of Neuronal Migration Disorders (Q33790169) (← links)
- Central nervous system malformations: locations of known human mutations (Q33793036) (← links)
- Lis1 reduction causes tangential migratory errors in mouse spinal cord (Q33835930) (← links)
- How to construct a neural tube (Q33850885) (← links)
- Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects (Q33851469) (← links)