אורלי ריינר פרופסור ישראלית לגנטיקה מולקולרית ולמדעי המוח המולקולריים
Reiner, Orly
Reiner, O.
ריינר, אורלי
VIAF ID: 58145304382378570974 (Personal)
Permalink: http://viaf.org/viaf/58145304382378570974
Preferred Forms
- 100 1 _ ‡a Reiner, O.
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- 100 0 _ ‡a אורלי ריינר ‡c פרופסור ישראלית לגנטיקה מולקולרית ולמדעי המוח המולקולריים
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4xx's: Alternate Name Forms (5)
Works
Title | Sources |
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Abnormal cortical development; towards elucidation of the LIS1 gene product function (review). | |
Alternative splice variants of doublecortin-like kinase are differentially expressed and have different kinase activities | |
Analysis of lissencephaly-causingLIS1mutations | |
Antagonistic effects of doublecortin and MARK2/Par-1 in the developing cerebral cortex. | |
Brain Organoids-A Bottom-Up Approach for Studying Human Neurodevelopment | |
Cdk5 checks p27kip1 in neuronal migration | |
Characterization of mutations in Gaucher patients by cDNA cloning | |
Cleavage of doublecortin-like kinase by calpain releases an active kinase fragment from a microtubule anchorage domain | |
Common and divergent roles for members of the mouse DCX superfamily. | |
Constitutive activation of canonical Wnt signaling disrupts choroid plexus epithelial fate | |
DCX in PC12 cells: CREB-mediated transcription and neurite outgrowth | |
DCX's phosphorylation by not just another kinase (JNK). | |
Developmental activities of the complement pathway in migrating neurons | |
Doublecortin-like kinase controls neurogenesis by regulating mitotic spindles and M phase progression. | |
Doublecortin-like kinase is associated with microtubules in neuronal growth cones. | |
Doublecortin mutations cluster in evolutionarily conserved functional domains | |
Doublecortin supports the development of dendritic arbors in primary hippocampal neurons. | |
Dynamics of cortical progenitors and production of subcerebral neurons are altered in embryos of a maternal inflammation model for autism | |
Efficient in vitro and in vivo expression of human glucocerebrosidase cDNA. | |
Evidence for the involvement of the hippocampus in the pathophysiology of schizophrenia | |
The evolving doublecortin (DCX) superfamily | |
Expression of chLIS1, a chicken homolog of LIS1. | |
Folding of proteins with WD-repeats: comparison of six members of the WD-repeat superfamily to the G protein beta subunit. | |
Gene trapping: an antibody-dependent approach for verifying integration in your favorite gene | |
Generation of topically transgenic rats by in utero electroporation and in vivo bioluminescence screening. | |
Human Brain Organoids on a Chip Reveal the Physics of Folding | |
The human glucocerebrosidase gene and pseudogene: structure and evolution | |
Human sphingolipid activator protein-1 and sphingolipid activator protein-2 are encoded by the same gene | |
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome | |
Interkinetic nuclear movement in the ventricular zone of the cortex. | |
International consensus recommendations on the diagnostic work-up for malformations of cortical development | |
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats | |
KIAA0369, doublecortin-like kinase, is expressed during brain development | |
Linking cytoplasmic dynein and transport of Rab8 vesicles to the midbody during cytokinesis by the doublecortin domain-containing 5 protein | |
LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules. | |
LIS1, CLIP-170's key to the dynein/dynactin pathway | |
LIS1 is a microtubule-associated phosphoprotein | |
LIS1. let's interact sometimes... (part 1). | |
LIS1-no more no less | |
LIS2, gene and pseudogene, homologous to LIS1 (lissencephaly 1), located on the short and long arms of chromosome 2 | |
Lissencephaly 1 linking to multiple diseases: mental retardation, neurodegeneration, schizophrenia, male sterility, and more | |
Lissencephaly. A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. | |
The lissencephaly gene product Lis1, a protein involved in neuronal migration, interacts with a nuclear movement protein, NudC | |
Loss of PAFAH1B2 reduces amyloid-β generation by promoting the degradation of amyloid precursor protein C-terminal fragments. | |
Mark/Par-1 marking the polarity of migrating neurons. | |
Microtubule dynamics alter the interphase nucleus | |
Migration cues induce chromatin alterations. | |
Missense mutations resulting in type 1 lissencephaly. | |
Modeling the autistic cell: iPSCs recapitulate developmental principles of syndromic and nonsyndromic ASD. | |
Ndel1-derived peptides modulate bidirectional transport of injected beads in the squid giant axon | |
Ndel1 palmitoylation: a new mean to regulate cytoplasmic dynein activity. | |
Neuronal migration and neurodegeneration: 2 sides of the same coin. | |
Non-cell autonomous and non-catalytic activities of ATX in the developing brain | |
Notch Activation by Shootin1 Opposing Activities on 2 Ubiquitin Ligases. | |
Novel functional features of the Lis-H domain: role in protein dimerization, half-life and cellular localization. | |
Nucleokinesis | |
PAF-AH Catalytic Subunits Modulate the Wnt Pathway in Developing GABAergic Neurons | |
Passage number is a major contributor to genomic structural variations in mouse iPSCs | |
Physical mapping of the gene for juvenile nephronophthisis (NPH1) by construction of a complete YAC contig of 7 Mb on chromosome 2q13. | |
Postnatal alterations of the inhibitory synaptic responses recorded from cortical pyramidal neurons in the Lis1/sLis1 mutant mouse | |
Proteomics insights into infantile neuronal ceroid lipofuscinosis (CLN1) point to the involvement of cilia pathology in the disease | |
Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit. | |
Regulation of neuronal migration, an emerging topic in autism spectrum disorders | |
Reversible Cysteine Acylation Regulates the Activity of Human Palmitoyl-Protein Thioesterase 1 (PPT1). | |
Shootin1 acts in concert with KIF20B to promote polarization of migrating neurons | |
Similarities and differences between the Wnt and reelin pathways in the forming brain. | |
Site-specific dephosphorylation of doublecortin (DCX) by protein phosphatase 1 (PP1). | |
The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanism. | |
Stress-activated protein kinase MKK7 regulates axon elongation in the developing cerebral cortex. | |
The structure of the N-terminal domain of the product of the lissencephaly gene Lis1 and its functional implications | |
Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization | |
Tau's role in the developing brain: implications for intellectual disability. | |
The unfolding story of two lissencephaly genes and brain development. | |
Use of RNA interference by in utero electroporation to study cortical development: the example of the doublecortin superfamily | |
Using multi-organ culture systems to study Parkinson's disease | |
Variations in genes regulating neuronal migration predict reduced prefrontal cognition in schizophrenia and bipolar subjects from mediterranean Spain: A preliminary study | |
הכרה ומשיכה בחיידק AZOSPITILLIUM BRASILENSE. |