The cause of sporadic Alzheimer's disease (AD) remains unclear. Given the growing evidence that protein aggregates can spread in a "prion-like" fashion, we reasoned that a small population of brain cells producing such "prion-like" particles due to a postzygotic acquired mutation would be sufficient to trigger the disease. Deep DNA sequencing technology should in principle allow the detection of such mosaics.status: publishe
Background: Mutations in amyloid precursor protein (APP), presenilin 1 (PSEN1) and presenilin 2 (PSE...
Somatic mutations during stem cell division are responsible for several cancers. In principle, a sim...
Next-generation genetic sequencing (NGS) technologies facilitate the screening of multiple genes lin...
The cause of sporadic Alzheimer's disease (AD) remains unclear. Given the growing evidence that prot...
Germline mutations ofAPP,PSEN1, andPSEN2 genes cause autosomal dominant Alzheimer disease (AD). Soma...
Three decades of genetic research in Alzheimer disease (AD) have substantially broadened our underst...
The human cerebral cortex makes up approximately 82% of the total brain mass, has 52 distinct Brodma...
Three decades of genetic research in Alzheimer disease (AD) have substantially broadened our underst...
Alzheimer’s disease (AD) is the commonest neurodegenerative disease worldwide. Rare familial cases m...
Alzheimer’s disease (AD) is a clinically heterogeneous neurodegenerative disease with a strong genet...
Next-generation sequencing techniques and genome-wide association study analyses have provided a hug...
Alzheimer’s disease (AD) is the most common cause of dementia worldwide and a leading cause of death...
The possible role of somatic copy number variations (CNVs) in Alzheimer's disease (AD) aetiology has...
Mutations in the Presenilin 1 (PSEN1) gene are the most common cause of autosomal dominant familial ...
Mosaicism, the presence of genomic differences between cells due to post-zygotic somatic mutations, ...
Background: Mutations in amyloid precursor protein (APP), presenilin 1 (PSEN1) and presenilin 2 (PSE...
Somatic mutations during stem cell division are responsible for several cancers. In principle, a sim...
Next-generation genetic sequencing (NGS) technologies facilitate the screening of multiple genes lin...
The cause of sporadic Alzheimer's disease (AD) remains unclear. Given the growing evidence that prot...
Germline mutations ofAPP,PSEN1, andPSEN2 genes cause autosomal dominant Alzheimer disease (AD). Soma...
Three decades of genetic research in Alzheimer disease (AD) have substantially broadened our underst...
The human cerebral cortex makes up approximately 82% of the total brain mass, has 52 distinct Brodma...
Three decades of genetic research in Alzheimer disease (AD) have substantially broadened our underst...
Alzheimer’s disease (AD) is the commonest neurodegenerative disease worldwide. Rare familial cases m...
Alzheimer’s disease (AD) is a clinically heterogeneous neurodegenerative disease with a strong genet...
Next-generation sequencing techniques and genome-wide association study analyses have provided a hug...
Alzheimer’s disease (AD) is the most common cause of dementia worldwide and a leading cause of death...
The possible role of somatic copy number variations (CNVs) in Alzheimer's disease (AD) aetiology has...
Mutations in the Presenilin 1 (PSEN1) gene are the most common cause of autosomal dominant familial ...
Mosaicism, the presence of genomic differences between cells due to post-zygotic somatic mutations, ...
Background: Mutations in amyloid precursor protein (APP), presenilin 1 (PSEN1) and presenilin 2 (PSE...
Somatic mutations during stem cell division are responsible for several cancers. In principle, a sim...
Next-generation genetic sequencing (NGS) technologies facilitate the screening of multiple genes lin...