Changes in DNA copy number, whether confined to specific genes or affecting whole chromosomes, have been identified as causes of diseases and developmental abnormalities and as sources of adaptive potential. Here, we discuss the costs and benefits of DNA copy-number alterations. Changes in DNA copy number are largely detrimental. Amplifications or deletions of specific genes can elicit discrete defects. Large-scale changes in DNA copy number can also cause detrimental phenotypes that are due to the cumulative effects of copy-number alterations of many genes simultaneously. On the other hand, studies in microorganisms show that DNA copy-number alterations can be beneficial, increasing survival under selective pressure. As DNA copy-number alt...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
<div><b>Human genes in pathogenic CNVs are dosage-sensitive and have constrained evolutionary copy n...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Changes in DNA copy number, whether confined to specific genes or affecting whole chromosomes, have ...
Abstract For a subset of genes in our genome a change in gene dosage, by duplication or deletion, ca...
Copy number variants (CNVs) overlap over 7000 genes, many of which are pivotal in biological pathway...
Contains fulltext : 88483.pdf (publisher's version ) (Closed access)The human geno...
Despite the long recognised effects of chromosomal structural abnormalities and completion of the Hu...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
Both endogenous and exogenous factors may damage DNA. DNA damage response genes work together in dif...
ABSTR ACT: Copy number variations (CNVs) are gains and losses of genomic sequence between two indivi...
Contains fulltext : 71198.pdf (publisher's version ) (Open Access)Copy number vari...
Copy number variants (CNVs) were the subject of extensive research in the past years. They are commo...
Copy number changes, the gains and losses of chromosome segments, are a common type of genetic varia...
Recent studies have unveiled copy number variants (CNVs) as an important source of genetic variation...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
<div><b>Human genes in pathogenic CNVs are dosage-sensitive and have constrained evolutionary copy n...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Changes in DNA copy number, whether confined to specific genes or affecting whole chromosomes, have ...
Abstract For a subset of genes in our genome a change in gene dosage, by duplication or deletion, ca...
Copy number variants (CNVs) overlap over 7000 genes, many of which are pivotal in biological pathway...
Contains fulltext : 88483.pdf (publisher's version ) (Closed access)The human geno...
Despite the long recognised effects of chromosomal structural abnormalities and completion of the Hu...
Genomic differences (mutations) in humans are profoundly influenced by their distinction as either g...
Both endogenous and exogenous factors may damage DNA. DNA damage response genes work together in dif...
ABSTR ACT: Copy number variations (CNVs) are gains and losses of genomic sequence between two indivi...
Contains fulltext : 71198.pdf (publisher's version ) (Open Access)Copy number vari...
Copy number variants (CNVs) were the subject of extensive research in the past years. They are commo...
Copy number changes, the gains and losses of chromosome segments, are a common type of genetic varia...
Recent studies have unveiled copy number variants (CNVs) as an important source of genetic variation...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
<div><b>Human genes in pathogenic CNVs are dosage-sensitive and have constrained evolutionary copy n...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...