官方服务:
资源简介:
LEOPARD Syndrome iPS, BJ iPS and Fibroblasts
应用场景:
创建时间:
2010-06-24
相关数据集
X-CGD iPS cells before and after genome editing by designer nucleases
X-CGD (X-linked chronic granulomatous disease) patient derived CD34+ cells were reprogrammed into two X-CGD iPSC clones (7 and 25) and subsequently corrected using ZFN (clone 7) and TALEN (clone 25) b
NIAID Data Ecosystem100
Genetic Neuroscience: How Human Genes and Alleles Shape Neuronal Phenotypes
The goal of this collaborative, interdisciplinary project is to develop powerful, generalizable approaches for discovering how risk variants for psychiatric disorders shape neurobiological processes a
NIAID Data Ecosystem30
Genome-wide analysis of base editing specificity in human iPSCs. Homo sapiens
Targeting specificity of genome editing tools is crucial for their applications in research and medicine. This project studies the specificity of cytosine base editor in human induced pluripotent stem
NIAID Data Ecosystem10
Impaired Telomere Maintenance and Decreased Canonical WNT Signaling but Normal Ribosome Biogenesis in Induced Pluripotent Stem Cells from X-Linked Dyskeratosis Congenita Patients
Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome characterized by the presence of short telomeres at presentation. Mutations in ten different genes, whose products are involved
NIAID Data Ecosystem70
Gene expression programs between genetically matched PEF and porcine iPSCs
Somatic cells gain pluripotency after transfection of Oct4, Sox2, Klf4, and cMyc (OSKM), and chromatin remodeling has been proved to be involved in this process. To date, chromatin accessibility in po
NIAID Data Ecosystem10



