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Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyriaImpaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficitsMutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypesClusters of iron-rich cells in the upper beak of pigeons are macrophages not magnetosensitive neuronsNew semidominant mutations that affect mouse developmentUner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stabilityMutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalities.Disease-associated mutations in TUBA1A result in a spectrum of defects in the tubulin folding and heterodimer assembly pathway.A gene-driven ENU-based approach to generating an allelic series in any gene.Determining sequences and post-translational modifications of novel conotoxins in Conus victoriae using cDNA sequencing and mass spectrometry.Therapeutic applications of conotoxins that target the neuronal nicotinic acetylcholine receptor.Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A).No evidence for intracellular magnetite in putative vertebrate magnetoreceptors identified by magnetic screening.N-ethyl-N-nitrosourea mouse mutants in the dissection of behavioural and psychiatric disorders.Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze TypeA pachygyria-causing alpha-tubulin mutation results in inefficient cycling with CCT and a deficient interaction with TBCB.Neuronal migration: unraveling the molecular pathway with humans, mice, and a fungus.Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia.Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation.Microtubules and neurodevelopmental disease: the movers and the makers.Scalable Technology for the Extraction of Pharmaceutics (STEP): the transition from academic knowhow to industrial reality.Brain-specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition.Mutations in the murine homologue of TUBB5 cause microcephaly by perturbing cell cycle progression and inducing p53-associated apoptosis.The Expression of Tubb2b Undergoes a Developmental Transition in Murine Cortical Neurons.Is magnetogenetics the new optogenetics?Tuba8 is expressed at low levels in the developing mouse and human brainCorrection: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes.Scalable technology for the extraction of pharmaceutics: outcomes from a 3 year collaborative industry/academia research programme.Magnetoreception-A sense without a receptor.An iron-rich organelle in the cuticular plate of avian hair cells.Exome sequencing can detect pathogenic mosaic mutations present at low allele frequencies.Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens.Subcellular analysis of pigeon hair cells implicates vesicular trafficking in cuticulosome formation and maintenance.Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.Behavioural characterisation of the robotic mouse mutant.Feasibility of scaling from pilot to process scale.Estimating the number of coding mutations in genotypic and phenotypic driven N-ethyl-N-nitrosourea (ENU) screens: revisited.Comment on "Magnetosensitive neurons mediate geomagnetic orientation in Caenorhabditis elegans".Cryptochrome: The magnetosensor with a sinister side?
P50
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P50
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Australian neuroscientist
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研究者
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David Anthony Keays
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David Keays
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David Keays
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David Anthony Keays
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David Keays
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David Keays
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David Anthony Keays
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0000-0002-8343-8002
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1976-01-01T00:00:00Z