Results 31 to 40 of about 2,797,849 (300)

Functional Deletion/Insertion Promoter Variants in SCARB1 Associated With Increased Susceptibility to Lipid Profile Abnormalities and Coronary Heart Disease

Frontiers in Cardiovascular Medicine, 2022
Background: Genetic variants in Scavenger receptor Class B Type 1 (SCARB1) influencing high-density lipoprotein cholesterol (HDL-C) and coronary heart disease (CHD) risk were identified by recent genome-wide association studies.
Senlin Hu, Senlin Hu, Dong Hu, Dong Hu, Haoran Wei, Haoran Wei, Shi-yang Li, Shi-yang Li, Dong Wang, Dong Wang, Chen-ze Li, Chen-ze Li, Jiangang Jiang, Jiangang Jiang, Daowen Wang, Daowen Wang, Guanglin Cui, Guanglin Cui, Daowu Wang   +18 more
doaj   +1 more source

Further Discussion on the Oath of the Rus… (Responding to D.V. Puzanov)

Ученые записки Казанского университета: Серия Гуманитарные науки
This article is a response to the criticism by D.V. Puzanov. The main arguments and counterarguments are summarized. New evidence is provided in favor of the hypothesis that the oaths taken by the pagan Rus and the Greeks to ratify the agreements between
О. L. Gubarev
doaj   +1 more source

The V5A13.1 envelope glycoprotein deletion mutant of mouse hepatitis virus type-4 is neuroattenuated by its reduced rate of spread in the central nervous system. [PDF]

, 1992
Following intracerebral inoculation of adult Balb/c Byj mice, the MHV-4 strain of mouse hepatitis virus (MHV) had an LD50 of less than 0.1 PFU, whereas its monoclonal antibody resistant variant V5A13.1 had an LD50 of 10(4.2) PFU.
Bloom, F, Buchmeier, MJ, Fazakerley, JK, Parker, SE   +3 more
core   +1 more source

Far-Field Tunable Nano-focusing Based on Metallic Slits Surrounded with Nonlinear-Variant Widths and Linear-Variant Depths of Circular Dielectric Grating

, 2013
In this work, we design a new tunable nanofocusing lens by the linear-variant depths and nonlinear-variant widths of circular grating for far field practical applications.
Cao, Peng-Fei, Cheng, Ling, Kong, Wei-Jie, Liang, Xue-Wu, Lu, Wei-Ping, Zhang, Xiao-Ping, 会议   +6 more
core   +1 more source

Mid-pass whole-genome sequencing in a Malagasy cohort uncovers body composition associations

HGG Advances
Summary: The majority of human genomic research studies have been conducted in European-ancestry cohorts, reducing the likelihood of detecting potentially novel and globally impactful findings. Here, we present mid-pass whole-genome sequencing data and a
Iman Hamid, Séverine Nantenaina Stéphie Raveloson, Germain Jules Spiral, Soanorolalao Ravelonjanahary, Brigitte Marie Raharivololona, José Mahenina Randria, Mosa Zafimaro, Tsiorimanitra Aimée Randriambola, Rota Mamimbahiny Andriantsoa, Tojo Julio Andriamahefa, Bodonomena Fitahiana Laza Rafidison, Mehreen Mughal, Anne-Katrin Emde, Melissa Hendershott, Sarah LeBaron von Baeyer, Kaja A. Wasik, Jean Freddy Ranaivoarisoa, Laura Yerges-Armstrong, Stephane E. Castel, Rindra Rakotoarivony   +19 more
doaj   +1 more source

New biothreat of JN.1 variant SARS CoV-2: viral genome, mutations and comparison with Delta and Omicron variants – a brief commentary [PDF]

Infectious Diseases and Tropical Medicine
SARS-CoV-2, the etiologic agent of COVID-19, is susceptible to mutations and emerged into many variants. This study aims to investigate a new variant called JN.1 with a remarkable number of mutations reported from many countries.
S. Kannan, U. Zeba, F. Razana, A. Huda, L. Punya, A. Sheeza, S. Salajegheh Tazerji, P. Magalhães Duarte   +7 more
doaj   +1 more source

SMaSH: A Benchmarking Toolkit for Human Genome Variant Calling

, 2014
Motivation: Computational methods are essential to extract actionable information from raw sequencing data, and to thus fulfill the promise of next-generation sequencing technology. Unfortunately, computational tools developed to call variants from human
Bresler, Ma'ayan, Curtis, Kristal, Hartl, Christopher, Jordan, Michael I., Liptrap, Jesse, Newcomb, Julie, Patterson, David, Song, Yun S., Talwalkar, Ameet, Terhorst, Jonathan   +9 more
core   +1 more source

Analysis of Archived Residual Newborn Screening Blood Spots After Whole Genome Amplification [PDF]

, 2015
Deidentified newborn screening bloodspot samples (NBS) represent a valuable potential resource for genomic research if impediments to whole exome sequencing of NBS deoxyribonucleic acid (DNA), including the small amount of genomic DNA in NBS material ...
Benstead-Hume, Graeme, Cantarel, Brandi L., Farrell, Andrew, Finnell, Richard H., Lei, Yunping, Reese, Justin, Weaver, Daniel, Zhu, Huiping   +7 more
core   +3 more sources

Folding variant narrowing and optimal variant termination [PDF]

The Journal of Logic and Algebraic Programming, 2010
S. Escobar has been partially supported by the EU (FEDER) and the Spanish MEC/MICINN under Grant TIN 2010-21062-C02-02, and by Generalitat Valenciana PROMETEO2011/052. R. Sasse and J. Meseguer have been partially supported by NSF Grants CNS 07-16638, CNS 08-31064, CNS 09-04749, and CCF 09-05584.
Escobar, Santiago, Sasse, Ralf, Meseguer, José   +2 more
openaire   +4 more sources

Why and When Are Evidence‐Based Interventions Adopted in Paediatric Supportive Care? A Qualitative Exploration of the Determinants of Photobiomodulation Implementation

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Oral mucositis is a common and debilitating side effect of childhood cancer and stem cell transplant treatments. It affects the quality of life of children and young people (CYP) and places a strain on services. Photobiomodulation is recommended for oral mucositis prevention in international guidance but is poorly implemented in UK ...
Claudia Heggie, Kara A. Gray‐Burrows, Peter F. Day, Bob Phillips, Carl A. Thompson   +4 more
wiley   +1 more source