Robin J Kleiman
Dados Biográficos
| ID | 7953915 |
|---|---|
| NOME | Robin J Kleiman |
| PRENOMES | Robin J |
| SOBRENOME | Kleiman |
| ASSINATURA | KLEIMAN R J |
| AFILIAÇÕES | Boston Children's Hospital |
| ORCID | 0000-0002-9415-7433 |
| VERIFICADO | Sim |
| TOTAL DE OBRAS | 1 |
| TOTAL DE CITAÇÕES | 0 |
| OBRAS COMO AUTOR | 1 |
| OBRAS COMO EDITOR | 0 |
| PRIMEIRO ANO DE PUBLICAÇÃO | 2022 |
| ANO MAIS RECENTE DE PUBLICAÇÃO | 2022 |
| ÍNDICE H | 0 |
P13.11 Deletion Variants Associated With Neuropsychiatric Disorders Cause Morphological and Synaptic Changes in Induced Pluripotent Stem Cell-Derived Neurons
16p13.11 copy number variants (CNVs) have been associated with autism, schizophrenia, psychosis, intellectual disability, and epilepsy. The majority of 16p13.11 deletions or duplications occur within three well-defined intervals, and despite growing knowledge of the functions of individual genes within these intervals, the molecular mechanisms that underlie commonly observed clinical phenotypes remain largely unknown. Patient-derived, induced plu…
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P13.11 Deletion Variants Associated With Neuropsychiatric Disorders Cause Morphological and Synaptic Changes in Induced Pluripotent Stem Cell-Derived Neurons
16p13.11 copy number variants (CNVs) have been associated with autism, schizophrenia, psychosis, intellectual disability, and epilepsy. The majority of 16p13.11 deletions or duplications occur within three well-defined intervals, and despite growing knowledge of the functions of individual genes within these intervals, the molecular mechanisms that underlie commonly observed clinical phenotypes remain largely unknown. Patient-derived, induced plu…
Biology (1 obra) · Congenital heart defects research (1 obra) · Copy-number variation (1 obra) · Embryonic stem cell (1 obra) · Gene (1 obra) · Gene expression (1 obra) · Genetics (1 obra) · Genetics and Neurodevelopmental Disorders (1 obra) · Genome (1 obra) · Genomic variations and chromosomal abnormalities (1 obra)