Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
Por um escritor misterioso
Last updated 04 setembro 2024
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PDF) Relevance of BET Family Proteins in SARS-CoV-2 Infection
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://iiif.elifesciences.org/lax:77848%2Felife-77848-fig2-v2.tif/full/,1500/0/default.jpg)
STAG2 promotes the myelination transcriptional program in oligodendrocytes
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://www.researchgate.net/publication/5585260/figure/fig2/AS:394662952095776@1471106388699/Rescue-of-Axon-Pruning-and-Proliferation-Defect-by-SMC1-transgene-A-B-SMC1--MB.png)
Rescue of Axon Pruning and Proliferation Defect by SMC1 transgene (A-B)
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://onlinelibrary.wiley.com/cms/asset/37590899-b17c-4395-816d-e8307cfcd73f/cge13674-fig-0001-m.jpg)
Chromatinopathies: A focus on Cornelia de Lange syndrome - Avagliano - 2020 - Clinical Genetics - Wiley Online Library
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://www.science.org/cms/10.1126/sciadv.abf7346/asset/eae172e3-a7c5-4fbb-817b-db9fc3f838cb/assets/graphic/abf7346-f1.jpeg)
Functional coordination of BET family proteins underlies altered transcription associated with memory impairment in fragile X syndrome
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41467-021-23141-9/MediaObjects/41467_2021_23141_Fig3_HTML.png)
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://www.cdls.org.uk/media/images/CdLS%20Figure%204.png)
What causes Cornelia de Lange Syndrome - CdLS Foundation UK and Ireland
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://wires.onlinelibrary.wiley.com/cms/asset/d8f11441-36c5-4763-98e4-75b055ea6feb/wrna1734-fig-0003-m.jpg)
Emerging roles of BET proteins in transcription and co‐transcriptional RNA processing - Eischer - 2023 - WIREs RNA - Wiley Online Library
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://www.mdpi.com/pharmaceuticals/pharmaceuticals-14-00765/article_deploy/html/images/pharmaceuticals-14-00765-g001.png)
Pharmaceuticals, Free Full-Text
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://www.researchgate.net/publication/353523238/figure/fig1/AS:1050565199003648@1627485670140/The-cohesin-complex-and-associated-proteins-A-Relevant-proteins-of-the-cohesin_Q320.jpg)
PDF) BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://d16qt3wv6xm098.cloudfront.net/2P9wJtK9QEu9ksG_4N5ad6XRQwmmhmcs/_.png)
Cornelia de Lange Syndrome: What Is It, Causes, Signs, Symptoms, and More
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41467-021-23141-9/MediaObjects/41467_2021_23141_Fig2_HTML.png)
Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://www.frontiersin.org/files/Articles/709232/fmolb-08-709232-HTML/image_m/fmolb-08-709232-t001.jpg)
Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome
![Frontiers BETting on a Transcriptional Deficit as the Main Cause for Cornelia de Lange Syndrome](https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41419-019-1792-x/MediaObjects/41419_2019_1792_Fig3_HTML.png)
The Cornelia de Lange Syndrome-associated factor NIPBL interacts with BRD4 ET domain for transcription control of a common set of genes
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