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Identification of Vulnerable Interneuron Subtypes in 15q13.3 Microdeletion Syndrome Using Single-Cell Transcriptomics
🌐 90 Days
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- Molecular cascades and cell type-specific signatures in ASD revealed by single-cell genomics
- Molecular cascades and cell type-specific signatures in ASD revealed by single-cell genomics
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- A single-cell and spatial RNA-seq database for Alzheimer's disease (ssREAD)
- Clinically unfavorable transcriptome subtypes of non-WNT/non-SHH medulloblastomas are associated with a predominance in proliferating and progenitor-like cell subpopulations
- Clinically unfavorable transcriptome subtypes of non-WNT/non-SHH medulloblastomas are associated with a predominance in proliferating and progenitor-like cell subpopulations
- Hofbauer cells and fetal brain microglia share transcriptional profiles and responses to maternal diet-induced obesity
- Hofbauer cells and fetal brain microglia share transcriptional profiles and responses to maternal diet-induced obesity
- Clinical and molecular genetic analysis of a child with comorbid 16p11.2 microdeletion syndrome and Rett syndrome
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- Single-cell genomics and regulatory networks for 388 human brains
- Single-cell genomics and regulatory networks for 388 human brains
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- Transcriptomics of Human Brain Tissue in Parkinson's Disease: a Comparison of Bulk and Single-cell RNA Sequencing
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- Artificial Intelligence-Based Non-invasive Differentiation of Distinct Histologic Subtypes of Renal Tumors With Multiphasic Multidetector Computed Tomography
- Developmental trajectories of GABAergic cortical interneurons are sequentially modulated by dynamic FoxG1 expression levels
- Selective vulnerability of the ventral hippocampus-prelimbic cortex axis parvalbumin interneuron network underlies learning deficits of fragile X mice
- Single-nucleus transcriptomics uncovers a geroprotective role of YAP in primate gingival aging
- Characterisation of premature cell senescence in Alzheimer's disease using single nuclear transcriptomics
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Identification of Vulnerable Interneuron Subtypes in 15q13.3 Microdeletion Syndrome Using Single-Cell Transcriptomics
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Identification of Vulnerable Interneuron Subtypes in 15q13.3 Microdeletion Syndrome Using Single-Cell Transcriptomics
🌐 365 Days
AI Virtual Reality Related Evidence Matrix
- MNMST: topology of cell networks leverages identification of spatial domains from spatial transcriptomics data
- Single-cell brain organoid screening identifies developmental defects in autism
- hdWGCNA identifies co-expression networks in high-dimensional transcriptomics data
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- Clinically unfavorable transcriptome subtypes of non-WNT/non-SHH medulloblastomas are associated with a predominance in proliferating and progenitor-like cell subpopulations
- Clinically unfavorable transcriptome subtypes of non-WNT/non-SHH medulloblastomas are associated with a predominance in proliferating and progenitor-like cell subpopulations
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- Hofbauer cells and fetal brain microglia share transcriptional profiles and responses to maternal diet-induced obesity
- Hofbauer cells and fetal brain microglia share transcriptional profiles and responses to maternal diet-induced obesity
- Single-cell mapping identifies MSI+ cells as a common origin for diverse subtypes of pancreatic cancer
- Clinical and molecular genetic analysis of a child with comorbid 16p11.2 microdeletion syndrome and Rett syndrome
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- Hypertension with hidden causes: the cognitive and behavioral profile of an adult female with chronic stress and 16p11.2 microdeletion
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- Single-cell genomics and regulatory networks for 388 human brains
- Single-cell genomics and regulatory networks for 388 human brains
- Single-cell genomics and regulatory networks for 388 human brains
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- Transcriptional changes in specific subsets of Drosophila neurons following inhibition of the serotonin transporter
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- Patient Brain Organoids Identify a Link between the 16p11.2 Copy Number Variant and the RBFOX1 Gene