דורון לנצט גנטיקאי ואימונולוג ישראלי
לנצט, דורון, 1948-
Lancet, Doron, 1948-
VIAF ID: 942169084883490310003 (Personal)
Permalink: http://viaf.org/viaf/942169084883490310003
Preferred Forms
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100 1 _ ‡a Lancet, Doron, ‡d 1948-
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100 0 _
‡a
דורון לנצט
‡c
גנטיקאי ואימונולוג ישראלי
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100 1 _ ‡a לנצט, דורון, ‡d 1948-
4xx's: Alternate Name Forms (6)
Works
| Title | Sources |
|---|---|
| Genotype phenotype correlations in Israeli colorectal cancer patients |
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| GESTALT: a workbench for automatic integration and visualization of large-scale genomic sequence analyses. |
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| GIFtS: annotation landscape analysis with GeneCards |
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| Glutathione S-transferases in rat olfactory epithelium: purification, molecular properties and odorant biotransformation |
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| Graded Autocatalysis Replication Domain |
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| The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts |
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| Harvesting the human genome: the Israeli perspective. |
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| High-resolution copy-number variation map reflects human olfactory receptor diversity and evolution |
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| HORDE: comprehensive resource for olfactory receptor genomics |
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| Human Gene-Centric Databases at the Weizmann Institute of Science: GeneCards, UDB, CroW 21 and HORDE |
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| Human olfaction: from genomic variation to phenotypic diversity |
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| The human olfactory transcriptome |
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| Identification and characterization of coding single-nucleotide polymorphisms within a human olfactory receptor gene cluster |
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| Identification of a Functional Risk Variant for Pemphigus Vulgaris in the ST18 Gene |
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| Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family-based, Arab-Israeli sample |
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| Identification of the gene causing mucolipidosis type IV. |
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| In-silico human genomics with GeneCards |
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| Initial sequencing and analysis of the human genome |
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| Introducing PIONEER: a project to harness big data in prostate cancer research |
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| Is the G72/G30 locus associated with schizophrenia? single nucleotide polymorphisms, haplotypes, and gene expression analysis |
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| LEMD3: the gene responsible for bone density disorders (osteopoikilosis). |
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| Lymphoblast and brain expression of AHI1 and the novel primate-specific gene, C6orf217, in schizophrenia and bipolar disorder |
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| MalaCards: A Comprehensive Automatically-Mined Database of Human Diseases. |
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| MalaCards: an integrated compendium for diseases and their annotation |
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| A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel |
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| Modular genes with metazoan-specific domains have increased tissue specificity. |
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| Molecular disease presentation in diabetic nephropathy. |
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| Molecular transduction in smell and taste |
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| Monoclonal antibodies to ciliary glycoproteins of frog olfactory neurons |
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| MOPED enables discoveries through consistently processed proteomics data |
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| MOPED: Model Organism Protein Expression Database |
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| Mucolipidosis type IV: novel MCOLN1 mutations in Jewish and non-Jewish patients and the frequency of the disease in the Ashkenazi Jewish population |
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| Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis |
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| Mutations and lethality in simulated prebiotic networks |
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| Mutations in AIFM1 cause an X-linked childhood cerebellar ataxia partially responsive to riboflavin. |
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| Mutations in olfactory signal transduction genes are not a major cause of human congenital general anosmia |
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| A new gene for the Charcot-Marie-Tooth disorder. |
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| Next-generation sequencing of patients with congenital anosmia |
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| NIPBL gene responsible for Cornelia de Lange syndrome, a severe developmental disorder. |
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| Non-redundant compendium of human ncRNA genes in GeneCards |
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| Noncoding deletions reveal a gene that is critical for intestinal function |
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| Novel definition files for human GeneChips based on GeneAnnot |
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| Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoire |
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| The olfactory receptor universe--from whole genome analysis to structure and evolution. |
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| Omics data management and annotation |
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| ORDB, HORDE, ODORactor and other on-line knowledge resources of olfactory receptor-odorant interactions |
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| PathCards: multi-source consolidation of human biological pathways |
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| Personal receptor repertoires: olfaction as a model. |
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| Pharmacogenetics of glatiramer acetate therapy for multiple sclerosis reveals drug-response markers. |
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| Polypeptide gp95. A unique glycoprotein of olfactory cilia with transmembrane receptor properties |
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| Population differences in the human functional olfactory repertoire |
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| Prediction of the odorant binding site of olfactory receptor proteins by human-mouse comparisons |
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| Primate evolution of an olfactory receptor cluster: diversification by gene conversion and recent emergence of pseudogenes |
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| Prospects of a computational origin of life endeavor |
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| Protobiotic Systems Chemistry Analyzed by Molecular Dynamics |
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| Quasispecies in population of compositional assemblies |
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| Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene |
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| Rational confederation of genes and diseases: NGS interpretation via GeneCards, MalaCards and VarElect |
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| Reproducibility: In praise of open research measures |
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| The RUNX3 gene--sequence, structure and regulated expression |
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| Search for hand osteoarthritis susceptibility locus on chromosome 6p12.3-p12.1. |
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| Self-Replication and Evolution in Primordial Mutually Catalytic Sets |
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| SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum |
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| Synthetic lethal hubs associated with vincristine resistant neuroblastoma |
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| Systematic inference of copy-number genotypes from personal genome sequencing data reveals extensive olfactory receptor gene content diversity |
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| Systems medicine and integrated care to combat chronic noncommunicable diseases |
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| Systems protobiology: origin of life in lipid catalytic networks |
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| TECPR2: a new autophagy link for neurodegeneration |
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| TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability |
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| Toward a comprehensive molecular analysis of olfactory transduction |
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| Toward More Transparent and Reproducible Omics Studies Through a Common Metadata Checklist and Data Publications |
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| The trace amine receptor 4 gene is not associated with schizophrenia in a sample linked to chromosome 6q23 |
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| The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence |
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| The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy |
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| A unified nomenclature for vertebrate olfactory receptors |
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| Update on the olfactory receptor (OR) gene superfamily |
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| USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses |
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| VarElect: the phenotype-based variation prioritizer of the GeneCards Suite |
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| Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios |
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| Why do young women smoke? V. Role of direct and interactive effects of nicotinic cholinergic receptor gene variation on neurocognitive function |
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| Widespread ectopic expression of olfactory receptor genes |
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