Down syndrome (DS, trisomy 21), is the most common viable chromosomal disorder, with an incidence of 1 in 800 live births. Its phenotypic characteristics include intellectual impairment and several other developmental abnormalities, for the majority of which the pathogenetic mechanisms remain unknown. Several models have been used to investigate the mechanisms by which the extra copy of chromosome 21 leads to the DS phenotype. In the last five years, several laboratories have been successful in reprogramming patient cells carrying the trisomy 21 anomaly into induced pluripotent stem cells, i.e., T21-iPSCs. In this review, we summarize the different T21-iPSCs that have been generated with a particular interest in the technical procedures and...
Trisomy of chromosome 21, the genetic cause of Down syndrome, has the potential to alter expression ...
Due to their underlying genetic complexity, chromosomal disorders such as Down syndrome (DS), which ...
Trisomy 21 is the most common chromosomal abnormality and is associated primarily with cardiovascula...
Down syndrome (DS) is a complex developmental disorder with diverse pathologies that affect multiple...
Down Syndrome (DS), or Trisomy 21 Syndrome, is one of the most common genetic diseases. It is a chro...
SummaryHuman trisomies can alter cellular phenotypes and produce congenital abnormalities such as Do...
Trisomy 21 (T21), Down Syndrome (DS) is the most common genetic cause of dementia and intellectual d...
Trisomy 21 (T21), Down Syndrome (DS) is the most common genetic cause of dementia and intellectual d...
Down syndrome (DS) is the most frequent cause of human congenital mental retardation. Cognitive defi...
Down syndrome is a genetic anomaly that manifests when there is a mistake during cell division, resu...
Down syndrome (trisomy 21) is the most common viable chromosomal disorder with intellectual impairme...
permits unrestricted use, distribution, and reproduction in any medium, provided the original work i...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...
Human induced pluripotent stem cells (iPSCs) have opened new possibilities to recapitulate disease m...
<div><p>Trisomy of chromosome 21, the genetic cause of Down syndrome, has the potential to alter exp...
Trisomy of chromosome 21, the genetic cause of Down syndrome, has the potential to alter expression ...
Due to their underlying genetic complexity, chromosomal disorders such as Down syndrome (DS), which ...
Trisomy 21 is the most common chromosomal abnormality and is associated primarily with cardiovascula...
Down syndrome (DS) is a complex developmental disorder with diverse pathologies that affect multiple...
Down Syndrome (DS), or Trisomy 21 Syndrome, is one of the most common genetic diseases. It is a chro...
SummaryHuman trisomies can alter cellular phenotypes and produce congenital abnormalities such as Do...
Trisomy 21 (T21), Down Syndrome (DS) is the most common genetic cause of dementia and intellectual d...
Trisomy 21 (T21), Down Syndrome (DS) is the most common genetic cause of dementia and intellectual d...
Down syndrome (DS) is the most frequent cause of human congenital mental retardation. Cognitive defi...
Down syndrome is a genetic anomaly that manifests when there is a mistake during cell division, resu...
Down syndrome (trisomy 21) is the most common viable chromosomal disorder with intellectual impairme...
permits unrestricted use, distribution, and reproduction in any medium, provided the original work i...
Down syndrome is the most common genetic cause of intellectual disability worldwide and affects more...
Human induced pluripotent stem cells (iPSCs) have opened new possibilities to recapitulate disease m...
<div><p>Trisomy of chromosome 21, the genetic cause of Down syndrome, has the potential to alter exp...
Trisomy of chromosome 21, the genetic cause of Down syndrome, has the potential to alter expression ...
Due to their underlying genetic complexity, chromosomal disorders such as Down syndrome (DS), which ...
Trisomy 21 is the most common chromosomal abnormality and is associated primarily with cardiovascula...