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Complex Congenital Heart Diseases
Complex congenital heart disease (CHD) includes a wide spectrum of anatomical anomalies. Most of complex CHDs are usually diagnosed with... -
Novel insights into the METTL3-METTL14 complex in musculoskeletal diseases
N6-methyladenosine (m 6 A) modification, catalyzed by methyltransferase complexes (MTCs), plays many roles in multifaceted biological activities. As...
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Exploring complex links: inflammatory rheumatic diseases and men's health
This article examines the complex interactions between inflammatory rheumatic diseases (IRDs) and men's health. It delves into the effects of IRDs on...
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Complex Forest Tree Diseases – Diagnostics Beyond Koch’s Postulates
Purpose of ReviewForest tree diseases are a major contributor to forest degradation and loss of productivity. They are often quite complex in their...
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Leveraging molecular quantitative trait loci to comprehend complex diseases/traits from the omics perspective
Comprehending the molecular basis of quantitative genetic variation is a principal goal for complex diseases or traits. Molecular quantitative trait...
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DGH-GO: dissecting the genetic heterogeneity of complex diseases using gene ontology
BackgroundComplex diseases such as neurodevelopmental disorders (NDDs) exhibit multiple etiologies. The multi-etiological nature of complex-diseases...
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An interactive atlas of genomic, proteomic, and metabolomic biomarkers promotes the potential of proteins to predict complex diseases
Multiomics analyses have identified multiple potential biomarkers of the incidence and prevalence of complex diseases. However, it is not known which...
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Deep migration learning-based recognition of diseases and insect pests in Yunnan tea under complex environments
BackgroundThe occurrence, development, and outbreak of tea diseases and pests pose a significant challenge to the quality and yield of tea,...
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Unravelling the complex causal effects of substance use behaviours on common diseases
BackgroundSubstance use behaviours (SUB) including smoking, alcohol consumption, and coffee intake are associated with many health outcomes. However,...
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Genetic regulation of m6A RNA methylation and its contribution in human complex diseases
N 6 -methyladenosine (m 6 A) has been established as the most prevalent chemical modification in message RNA (mRNA), playing an essential role in...
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Leveraging polygenic enrichments of gene features to predict genes underlying complex traits and diseases
Genome-wide association studies (GWASs) are a valuable tool for understanding the biology of complex human traits and diseases, but associated...
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MODILM: towards better complex diseases classification using a novel multi-omics data integration learning model
BackgroundAccurately classifying complex diseases is crucial for diagnosis and personalized treatment. Integrating multi-omics data has been...
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The emerging role of the piRNA/PIWI complex in respiratory tract diseases
PIWI-interacting RNA (piRNA) is a class of recently discovered small non-coding RNA molecules with a length of 18–33 nt that interacts with the PIWI...
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Identifying critical transitions in complex diseases
Mortality and the burden of diseases worldwide continue to reach substantial numbers with societal development and urbanization. In the face of...
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Consanguinity, complex diseases and congenital disabilities in the Souss population (Southern Morocco): a cross-sectional survey
BackgroundSeveral studies showed that the perpetuation of consanguinity increases homozygosity and homogenizes the population's gene pool. This...
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Early infectious diseases identification based on complex probabilistic hesitant fuzzy N-soft information
This paper aims to assess and deal with the challenges experienced by medical professionals caring for infectious diseases. In Pakistan, public...
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Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
A ~ 1 Mb inversion polymorphism exists within the 17q21.31 locus of the human genome as direct (H1) and inverted (H2) haplotype clades. This...
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Objectivizing issues in the diagnosis of complex rare diseases: lessons learned from testing existing diagnosis support systems on ciliopathies
BackgroundThere are approximately 8,000 different rare diseases that affect roughly 400 million people worldwide. Many of them suffer from delayed...
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Immune-response 3′UTR alternative polyadenylation quantitative trait loci contribute to variation in human complex traits and diseases
Genome-wide association studies (GWASs) have identified thousands of non-coding variants that are associated with human complex traits and diseases....
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Association between exposure to air pollutants and allergic diseases among residents near the Gwangyang industrial complex in Korea
ObjectiveThe purpose of this study is to characterize the levels of particulate matter (PM 10 ) and heavy metals (HMs) such as Cd and Pb, compare...