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2.
Fisc Stud ; 41(2): 321-336, 2020 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-32836540

RESUMO

The COVID-19 emergency has had a dramatic impact on market incomes and income-support policies. The lack of timely available data constrains the estimation of the scale and direction of recent changes in the income distribution, which in turn constrains policymakers seeking to monitor such developments. We overcome the lack of data by proposing a dynamic calibrated microsimulation approach to generate counterfactual income distributions as a function of more timely external data than are available in dated income surveys. We combine nowcasting methods using publicly available data and a household income generation model to perform the first calibrated simulation based upon actual data, aiming to assess the distributional implications of the COVID-19 crisis in Ireland. Overall, we find that the crisis had an equalizing real-time effect for both gross and disposable incomes, notwithstanding the significant hardship experienced by many households.

4.
Eur J Hum Genet ; 10(12): 865-9, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12461695

RESUMO

A consanguineous Arab pedigree in which recessive amelogenesis imperfecta (AI) and cone-rod dystrophy cosegregate, was screened for linkage to known retinal dystrophy and tooth abnormality loci by genotyping neighbouring microsatellite markers. This analysis resulted in linkage with a maximum lod score of 7.03 to the marker D2S2187 at the achromatopsia locus on chromosome 2q11, and haplotype analysis placed the gene(s) involved in a 2 cM/5 Mb interval between markers D2S2209 and D2S373. The CNGA3 gene, known to be involved in achromatopsia, lies in this interval but thorough analysis of its coding sequence revealed no mutation. Furthermore, affected individuals in four consanguineous recessive pedigrees with AI but without CRD were heterozygous at this locus, excluding it as a common cause of non-syndromic recessive AI. It remains to be established whether this pedigree is segregating two closely linked mutations causing disparate phenotypes or whether a single defect is causing pathology in both teeth and eyes.


Assuntos
Amelogênese Imperfeita/genética , Cromossomos Humanos Par 2/genética , Genes Recessivos/genética , Retinose Pigmentar/genética , Sequência de Bases , Mapeamento Cromossômico , Canais de Cátion Regulados por Nucleotídeos Cíclicos , Análise Mutacional de DNA , Feminino , Humanos , Canais Iônicos/genética , Escore Lod , Masculino , Dados de Sequência Molecular , Linhagem
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