GIFtS: annotation landscape analysis with GeneCardsInitial sequencing and analysis of the human genomeLoss of olfactory receptor genes coincides with the acquisition of full trichromatic vision in primatesGenetic elucidation of human hyperosmia to isovaleric acidAncient genomic architecture for mammalian olfactory receptor clustersQuasispecies in population of compositional assembliesIn-silico human genomics with GeneCardsOrganization and evolution of olfactory receptor genes on human chromosome 11Human specific loss of olfactory receptor genesThe genome of a songbirdGenome analysis of the platypus reveals unique signatures of evolutionWhy do young women smoke? V. Role of direct and interactive effects of nicotinic cholinergic receptor gene variation on neurocognitive functionThe UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergenceOlfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoireSequence analysis in the olfactory receptor gene cluster on human chromosome 17: recombinatorial events affecting receptor diversityNatural selection on the olfactory receptor gene family in humans and chimpanzeesMalaCards: an integrated compendium for diseases and their annotationGeneCards Version 3: the human gene integratorCongenital dyserythropoietic anemia type I is caused by mutations in codanin-1MOPED: Model Organism Protein Expression DatabaseThe H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcriptsHuman Gene-Centric Databases at the Weizmann Institute of Science: GeneCards, UDB, CroW 21 and HORDEGeneTide--Terra Incognita Discovery Endeavor: a new transcriptome focused member of the GeneCards/GeneNote suite of databasesConservation anchors in the vertebrate genomeA missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from IsraelMucolipidosis type IV: novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish populationThe UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathyAHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophreniaThe trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured searchORDB, HORDE, ODORactor and other on-line knowledge resources of olfactory receptor-odorant interactionsToward more transparent and reproducible omics studies through a common metadata checklist and data publicationsCoevolution of compositional protocells and their environmentA probabilistic classifier for olfactory receptor pseudogenesFrom subgenome analysis to protein structure.Systems medicine and integrated care to combat chronic noncommunicable diseases.Genome sequence of the pattern forming Paenibacillus vortex bacterium reveals potential for thriving in complex environments.Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy.The olfactory receptor gene superfamily: data mining, classification, and nomenclature.MOPED enables discoveries through consistently processed proteomics data.
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P50
description
Israeli life sciences researcher
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investigador israelí
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investigador israelín
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onderzoeker uit Israël
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name
Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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type
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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prefLabel
Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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Doron Lancet
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P101
P1960
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