Results 251 to 260 of about 12,100,252 (298)
CRHR1 Gene Copy Number Variations, Chronic Viral Infections, and Age as Correlates of Cognitive Impairment in Adults After SARS-CoV-2 Infection. [PDF]
Curr Issues Mol BiolHovhannisyan Y +4 more
europepmc +1 more source
Unraveling the missing heritability of amyotrophic lateral sclerosis: Should we focus more on copy number variations? [PDF]
Neural Regen ResGuarnaccia M +4 more
europepmc +1 more source
Genome-Wide Analysis of Copy Number Variations in Three Populations of Nanyang Cattle Using Whole-Genome Resequencing. [PDF]
Genes (Basel)Dang D +5 more
europepmc +1 more source
In Situ Inference of Copy Number Variations in Image-Based Spatial Transcriptomics
Jensen AEV +7 more
europepmc +1 more source
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Nature Reviews Microbiology, 2020
This study reports that extensive copy number variations occur in the presence of azole antifungal drugs in Candida albicans, which might cause phenotypic and population-level heterogeneity observed in clinical isolates.
Andrea du Toit
exaly +4 more sources
This study reports that extensive copy number variations occur in the presence of azole antifungal drugs in Candida albicans, which might cause phenotypic and population-level heterogeneity observed in clinical isolates.
Andrea du Toit
exaly +4 more sources
2018
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversions and copy number variants (CNVs, gain or loss of DNA). The latter can range from sub-microscopic events to complete chromosomal aneuploidies. Small CNVs are often benign but those larger than 250 kb are strongly associated with morbid consequences ...
Macé, Aurélien +2 more
openaire +5 more sources
Differences between genomes can be due to single nucleotide variants (SNPs), translocations, inversions and copy number variants (CNVs, gain or loss of DNA). The latter can range from sub-microscopic events to complete chromosomal aneuploidies. Small CNVs are often benign but those larger than 250 kb are strongly associated with morbid consequences ...
Macé, Aurélien +2 more
openaire +5 more sources
2010
Recent genetic epidemiology studies have been dominated by genome-wide association (GWA) studies using single nucleotide polymorphisms (SNPs). However, a form of structural genomic variation, termed copy number variation (CNV), is also widespread throughout the human genome, and can be highly polymorphic between individuals.
Wain, LV, Tobin, MD
openaire +3 more sources
Recent genetic epidemiology studies have been dominated by genome-wide association (GWA) studies using single nucleotide polymorphisms (SNPs). However, a form of structural genomic variation, termed copy number variation (CNV), is also widespread throughout the human genome, and can be highly polymorphic between individuals.
Wain, LV, Tobin, MD
openaire +3 more sources
Copy number variation and mosaicism
Cytogenetic and Genome Research, 2008Mosaicism is the presence of cells within an organism that have a different genetic composition despite deriving from a single zygote. The consequence of this depends on the number and type of cells that are affected as well as the specific DNA involved.
A J, Notini, J M, Craig, S J, White
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Copy number variations and cancer susceptibility
Current Opinion in Oncology, 2010DNA copy number variations (CNVs) comprise a recently discovered element of genetic variation that affects a greater cumulative fraction of the genome than single-nucleotide polymorphisms (SNPs). This review discusses current understanding of the characteristics of CNVs in the human genome and explores the emerging discoveries of both constitutional ...
Adam, Shlien, David, Malkin
openaire +2 more sources