about
The requirement of pax6 for postnatal eye development: evidence from experimental mouse chimerasVAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P(2) in yeast and mouse.PolymiRTS Database: linking polymorphisms in microRNA target sites with complex traitsConsensus paper: pathological role of the cerebellum in autismDab2IP GTPase activating protein regulates dendrite development and synapse number in cerebellumScrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in miceDevelopmental expression of the GIRK family of inward rectifying potassium channels: implications for abnormalities in the weaver mutant mouseDisrupted retinal development in the embryonic belly spot and tail mutant mouseFoxn3 is essential for craniofacial development in mice and a putative candidate involved in human congenital craniofacial defectsCellular localization and development of neuronal intranuclear inclusions in striatal and cortical neurons in R6/2 transgenic miceHuntingtin inhibits caspase-3 activationAnalysis of cerebellar development in math1 null embryos and chimerasA Novel and Multivalent Role of Pax6 in Cerebellar Development.Wls provides a new compartmental view of the rhombic lip in mouse cerebellar development.Genome-wide microarray comparison reveals downstream genes of Pax6 in the developing mouse cerebellum.A transgenic mouse class-III beta tubulin reporter using yellow fluorescent protein.Phenotype screening for genetically determined age-onset disorders and increased longevity in ENU-mutagenized miceENU induced single mutation locus on chr 16 leads to high-frequency hearing loss in miceHigh-throughput behavioral phenotyping in the expanded panel of BXD recombinant inbred strains.Identification of a set of genes showing regionally enriched expression in the mouse brainPreliminary analysis of the mouse cerebellum proteome.Non-coding-regulatory regions of human brain genes delineated by bacterial artificial chromosome knock-in mice.Studies on the hippocampal formation: From basic development to clinical applications: Studies on schizophreniaRepetitive behavior and increased activity in mice with Purkinje cell loss: a model for understanding the role of cerebellar pathology in autismGlutamate dysfunction associated with developmental cerebellar damage: relevance to autism spectrum disordersMolecular pathways underpinning ethanol-induced neurodegeneration.Sequence interpretation. Functional annotation of mouse genome sequences.Standards for the publication of mouse mutant studies.Behavioral flexibility in a mouse model of developmental cerebellar Purkinje cell lossA regulatory toolbox of MiniPromoters to drive selective expression in the brainPhenotypic and genetic analysis of the cerebellar mutant tmgc26, a new ENU-induced ROR-alpha alleleA promoter-level mammalian expression atlasInherited neuroaxonal dystrophy in dogs causing lethal, fetal-onset motor system dysfunction and cerebellar hypoplasia.Wild-type cells rescue genotypically Math1-null hair cells in the inner ears of chimeric mice.The cells and molecules that make a cerebellum.Dopamine dynamics associated with, and resulting from, schedule-induced alcohol self-administration: analyses in dopamine transporter knockout mice.Identification of genetic loci that modulate cell proliferation in the adult rostral migratory stream using the expanded panel of BXD mice.Conserved and differential gene interactions in dynamical biological systems.CAGE-defined promoter regions of the genes implicated in Rett Syndrome.Wild-type huntingtin plays a role in brain development and neuronal survival.
P50
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P50
description
hulumtues
@sq
onderzoeker
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researcher
@en
հետազոտող
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name
Daniel Goldowitz
@ast
Daniel Goldowitz
@en
Daniel Goldowitz
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Daniel Goldowitz
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Daniel Goldowitz
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type
label
Daniel Goldowitz
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Daniel Goldowitz
@en
Daniel Goldowitz
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Daniel Goldowitz
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Daniel Goldowitz
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D Goldowitz
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prefLabel
Daniel Goldowitz
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Daniel Goldowitz
@en
Daniel Goldowitz
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Daniel Goldowitz
@nl
Daniel Goldowitz
@sl
P106
P1153
7006144166
P21
P2456
P31
P4012
P496
0000-0003-4756-4017