Cargando…

Large-scale frequent testing and tracing to supplement control of Covid-19 and vaccination rollout constrained by supply

Non-pharmaceutical interventions (NPI) were implemented all around the world in the fight against COVID-19: Social distancing, shelter-in-place, mask wearing, etc. to mitigate transmission, together with testing and contact-tracing to identify, isolate and treat the infected. The majority of countri...

Descripción completa

Detalles Bibliográficos
Autores principales:	Humphrey, Lia, Thommes, Edward W., Fields, Roie, Coudeville, Laurent, Hakim, Naseem, Chit, Ayman, Wu, Jianhong, Cojocaru, Monica G.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	KeAi Publishing 2021
Materias:	Vaccination and Mutation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8302824/ https://www.ncbi.nlm.nih.gov/pubmed/34337194 http://dx.doi.org/10.1016/j.idm.2021.06.008

Ejemplares similares

Evaluating the sensitivity of SARS-CoV-2 infection rates on college campuses to wastewater surveillance
por: Wong, Tony E., et al.
Publicado: (2021)

Mathematical models for assessing vaccination scenarios in several provinces in Indonesia
por: Nuraini, N., et al.
Publicado: (2021)

Switched forced SEIRDV compartmental models to monitor COVID-19 spread and immunization in Italy
por: Antonelli, Erminia, et al.
Publicado: (2021)

Will vaccine-derived protective immunity curtail COVID-19 variants in the US?
por: Mancuso, Marina, et al.
Publicado: (2021)

Multi-generational SIR modeling: Determination of parameters, epidemiological forecasting and age-dependent vaccination policies
por: Campos, Eduardo Lima, et al.
Publicado: (2021)

Dynamics of COVID-19 pandemic in India and Pakistan: A metapopulation modelling approach
por: Brozak, Samantha J., et al.
Publicado: (2021)

Implementation of a real-time, data-driven online Epidemic Calculator for tracking the spread of COVID-19 in Singapore and other countries
por: Yap, Fook Fah, et al.
Publicado: (2021)

Vaccine efficacy and SARS-CoV-2 control in California and U.S. during the session 2020–2026: A modeling study
por: Mahmud, Md Shahriar, et al.
Publicado: (2021)

Optimizing COVID-19 vaccination programs during vaccine shortages
por: Liu, Kaihui, et al.
Publicado: (2022)

Identification of an unknown frameshift variant of NOG in a Han Chinese family with proximal symphalangism
por: Yuan, Zhuang-Zhuang, et al.
Publicado: (2020)

Identification of a frame shift mutation in the CCDC151 gene in a Han-Chinese family with Kartagener syndrome
por: Deng, Sheng, et al.
Publicado: (2020)

The association between Interleukin-6 rs1800795/rs1800797 polymorphisms and risk of rotator cuff tear in a Chinese population
por: Li, Jin, et al.
Publicado: (2020)

Reply to comments on: “Obesity associated with a novel mitochondrial tRNA(Cys) 5802A>G mutation in a Chinese family”
por: Wang, Jinling, et al.
Publicado: (2020)

Role of matrix metalloproteases 1/3 gene polymorphisms in patients with rotator cuff tear
por: Miao, Kaisong, et al.
Publicado: (2019)

Mitochondrial tRNA mutations in Chinese children with tic disorders
por: Jiang, Peifang, et al.
Publicado: (2020)

Characterization of functionally deficient SIM2 variants found in patients with neurological phenotypes
por: Button, Emily L., et al.
Publicado: (2022)

Genetic variants and haplotypes in fibulin-5 (FBLN5) are associated with pseudoexfoliation glaucoma but not with pseudoexfoliation syndrome
por: Kapuganti, Ramani Shyam, et al.
Publicado: (2023)

Molecular Spectrum of Autosomal Dominant Hypercholesterolemia in France
por: Marduel, Marie, et al.
Publicado: (2010)

A Rare Novel Deletion of the Tyrosine Hydroxylase Gene in Parkinson Disease
por: Bademci, Güney, et al.
Publicado: (2010)

Evaluation of Germline BMP4 Mutation as a Cause of Colorectal Cancer
por: Lubbe, Steven J, et al.
Publicado: (2011)

Plectin Deficiency Leads to Both Muscular Dystrophy and Pyloric Atresia in Epidermolysis Bullosa Simplex
por: Natsuga, Ken, et al.
Publicado: (2010)

Mutations and Deletions in PCDH19 Account for Various Familial or Isolated Epilepsies in Females
por: Depienne, Christel, et al.
Publicado: (2011)

Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome
por: Maselli, R A, et al.
Publicado: (2009)

A Novel Mutation in CRYBB1 Associated with Congenital Cataract-Microcornea Syndrome: The p.Ser129Arg Mutation Destabilizes the βB1/βA3-crystallin Heteromer But Not the βB1-crystallin Homomer
por: Wang, Kai Jie, et al.
Publicado: (2011)

Clinical and genetic spectrum of Birt–Hogg–Dubé syndrome patients in whom pneumothorax and/or multiple lung cysts are the presenting feature
por: Kunogi, Makiko, et al.
Publicado: (2010)

Lynch Syndrome-associated Mutations in MSH2 Alter DNA Repair and Checkpoint Response Functions In Vivo
por: Mastrocola, Adam S, et al.
Publicado: (2010)

Genetic Etiology of Parkinson Disease Associated with Mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 Genes: A Mutation Update
por: Nuytemans, Karen, et al.
Publicado: (2010)

Cerebral Arterial Stenoses and Stroke: Novel Features of Aicardi-Goutières Syndrome Caused by the Arg164X Mutation in SAMHD1 Are Associated with Altered Cytokine Expression
por: Thiele, Holger, et al.
Publicado: (2010)

Identification of FOXP1 Deletions in Three Unrelated Patients with Mental Retardation and Significant Speech and Language Deficits
por: Horn, Denise, et al.
Publicado: (2010)

A Novel CRYGD Mutation (p.Trp43Arg) Causing Autosomal Dominant Congenital Cataract in a Chinese Family
por: Wang, Binbin, et al.
Publicado: (2011)

Mutation Spectrum of EYS in Spanish Patients with Autosomal Recessive Retinitis Pigmentosa
por: Barragán, Isabel, et al.
Publicado: (2010)

A Novel Germline CDKN1B Mutation Causing Multiple Endocrine Tumors: Clinical, Genetic and Functional Characterization
por: Molatore, Sara, et al.
Publicado: (2010)

Adenine DNA Glycosylase Activity of 14 Human MutY Homolog (MUTYH) Variant Proteins Found in Patients with Colorectal Polyposis and Cancer
por: Goto, Masanori, et al.
Publicado: (2010)

Evaluating Self-declared Ancestry of U.S. Americans with Autosomal, Y-chromosomal and Mitochondrial DNA
por: Lao, Oscar, et al.
Publicado: (2010)

Legius Syndrome in Fourteen Families
por: Denayer, Ellen, et al.
Publicado: (2011)

The Clinical Spectrum of Missense Mutations of the First Aspartic Acid of cbEGF-like Domains in Fibrillin-1 Including a Recessive Family
por: Hilhorst-Hofstee, Yvonne, et al.
Publicado: (2010)

Identification and Characterization of 15 Novel GALC Gene Mutations Causing Krabbe Disease
por: Tappino, Barbara, et al.
Publicado: (2010)

Genetic Screening of LCA in Belgium: Predominance of CEP290 and Identification of Potential Modifier Alleles in AHI1 of CEP290-related Phenotypes
por: Coppieters, Frauke, et al.
Publicado: (2010)

Congenital Insensitivity to Pain: Novel SCN9A Missense and In-Frame Deletion Mutations
por: Cox, James J, et al.
Publicado: (2010)

Transcriptional and Translational Effects of Intronic CAPN3 Gene Mutations
por: Nascimbeni, Anna Chiara, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_01b77o10r5frhb53gbv0keeol7