The CNVs in (A) DNASE1L3 and (B) DNASE2. The genomic structures of each DNase gene were based upon the NCBI Reference Sequence: NG_032070.1 and NC_000019.10, respectively. All the CNVs in each gene were registered in the Database of Genomic Variants (http://dgv.tcag.ca/gb2/gbrowse/dgv2_hg38/). The black and gray bars indicate gain and loss of copy, respectively, in the CNVs. The regions of the gene shown by the dashed lines are the target regions used for Q-PCR analysis of each gene.</p
Genetic variations within the human genome can take many forms, including single-nucleotide polymorp...
Copy Number Variation (CNV) refers to duplication or deletion in the DNA sequence. Studying the patt...
Genomic copy number variants (CNVs) are a common, heritable source of inter-individual differences i...
Deoxyribonucleases (DNases) might play a role in prevention of autoimmune conditions such as systemi...
Deoxyribonucleases (DNases) might play a role in prevention of autoimmune conditions such as systemi...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variants (CNVs) were the subject of extensive research in the past years. They are commo...
A reduction of deoxyribonuclease I (DNase I) activity levels in the serum of patients with autoimmun...
Copy number variants (CNVs) overlap over 7000 genes, many of which are pivotal in biological pathway...
The human genome is rich in genomic regions that are repeated several times. These regions are known...
Copy number variants (CNVs) account for a major proportion of human genetic polymorphism and have be...
Structural variations of DNA greater than 1 kilobase in size account for most bases that vary among ...
<p><b>Objective</b>: To continue our previous investigations, we have extensively investigated the f...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Genomic copy number variants (CNVs) are a common, heritable source of inter-individual differences i...
Genetic variations within the human genome can take many forms, including single-nucleotide polymorp...
Copy Number Variation (CNV) refers to duplication or deletion in the DNA sequence. Studying the patt...
Genomic copy number variants (CNVs) are a common, heritable source of inter-individual differences i...
Deoxyribonucleases (DNases) might play a role in prevention of autoimmune conditions such as systemi...
Deoxyribonucleases (DNases) might play a role in prevention of autoimmune conditions such as systemi...
Copy number variations (CNVs) are universal genetic variations, and their association with disease h...
Copy number variants (CNVs) were the subject of extensive research in the past years. They are commo...
A reduction of deoxyribonuclease I (DNase I) activity levels in the serum of patients with autoimmun...
Copy number variants (CNVs) overlap over 7000 genes, many of which are pivotal in biological pathway...
The human genome is rich in genomic regions that are repeated several times. These regions are known...
Copy number variants (CNVs) account for a major proportion of human genetic polymorphism and have be...
Structural variations of DNA greater than 1 kilobase in size account for most bases that vary among ...
<p><b>Objective</b>: To continue our previous investigations, we have extensively investigated the f...
Copy number variation (CNV) of DNA sequences is functionally significant but has yet to be fully asc...
Genomic copy number variants (CNVs) are a common, heritable source of inter-individual differences i...
Genetic variations within the human genome can take many forms, including single-nucleotide polymorp...
Copy Number Variation (CNV) refers to duplication or deletion in the DNA sequence. Studying the patt...
Genomic copy number variants (CNVs) are a common, heritable source of inter-individual differences i...