Individuals with partial HSA21 trisomies and mice with partial MMU16 trisomies containing an extra copy of the DYRK1A gene present various alterations in brain morphogenesis. They present also learning impairments modeling those encountered in Down syndrome. Previous MRI and histological analyses of a transgenic mice generated using a human YAC construct that contains five genes including DYRK1A reveal that DYRK1A is involved, during development, in the control of brain volume and cell density of specific brain regions. Gene dosage correction induces a rescue of the brain volume alterations. DYRK1A is also involved in the control of synaptic plasticity and memory consolidation. Increased gene dosage results in brain morphogenesis defects, l...
CDKL5 deficiency disorder (CDD) is a rare X-linked neurodevelopmental disorder that is characterised...
CDKL5 deficiency disorder (CDD) is a rare X-linked neurodevelopmental disorder that is characterised...
CDKL5 deficiency disorder (CDD) is a rare X-linked neurodevelopmental disorder that is characterised...
Individuals with partial HSA21 trisomies and mice with partial MMU16 trisomies containing an extra c...
Individuals with partial HSA21 trisomies and mice with partial MMU16 trisomies containing an extra c...
Down syndrome (DS), caused by trisomy of chromosome 21, is the most common genetic cause of intellec...
Down syndrome (DS) is a genetic disorder caused by trisomy of chromosome 21 that leads to cognitive ...
Down syndrome (DS) is a genetic disorder caused by trisomy of chromosome 21 that leads to cognitive ...
Epigallocatechin gallate (EGCG) is an inhibitor of DYRK1A, a serine/threonine kinase considered to b...
International audienceEpigallocatechin gallate (EGCG) is an inhibitor of DYRK1A, a serine/threonine ...
International audienceDown syndrome is a common genetic disorder caused by trisomy of chromosome 21....
International audienceDown syndrome is a common genetic disorder caused by trisomy of chromosome 21....
International audienceDown syndrome is a common genetic disorder caused by trisomy of chromosome 21....
Down syndrome (DS) is caused by three copies of human chromosome 21 (Hsa21) and results in an array ...
Down Syndrome (DS), a genetic disorder that affects ~1 in 700 live births, is caused by trisomy of h...
CDKL5 deficiency disorder (CDD) is a rare X-linked neurodevelopmental disorder that is characterised...
CDKL5 deficiency disorder (CDD) is a rare X-linked neurodevelopmental disorder that is characterised...
CDKL5 deficiency disorder (CDD) is a rare X-linked neurodevelopmental disorder that is characterised...
Individuals with partial HSA21 trisomies and mice with partial MMU16 trisomies containing an extra c...
Individuals with partial HSA21 trisomies and mice with partial MMU16 trisomies containing an extra c...
Down syndrome (DS), caused by trisomy of chromosome 21, is the most common genetic cause of intellec...
Down syndrome (DS) is a genetic disorder caused by trisomy of chromosome 21 that leads to cognitive ...
Down syndrome (DS) is a genetic disorder caused by trisomy of chromosome 21 that leads to cognitive ...
Epigallocatechin gallate (EGCG) is an inhibitor of DYRK1A, a serine/threonine kinase considered to b...
International audienceEpigallocatechin gallate (EGCG) is an inhibitor of DYRK1A, a serine/threonine ...
International audienceDown syndrome is a common genetic disorder caused by trisomy of chromosome 21....
International audienceDown syndrome is a common genetic disorder caused by trisomy of chromosome 21....
International audienceDown syndrome is a common genetic disorder caused by trisomy of chromosome 21....
Down syndrome (DS) is caused by three copies of human chromosome 21 (Hsa21) and results in an array ...
Down Syndrome (DS), a genetic disorder that affects ~1 in 700 live births, is caused by trisomy of h...
CDKL5 deficiency disorder (CDD) is a rare X-linked neurodevelopmental disorder that is characterised...
CDKL5 deficiency disorder (CDD) is a rare X-linked neurodevelopmental disorder that is characterised...
CDKL5 deficiency disorder (CDD) is a rare X-linked neurodevelopmental disorder that is characterised...