Loss of Fnip1 alters kidney developmental transcriptional program and synergizes with TSC1 loss to promote mTORC1 activation and renal cyst formation.
Birt-Hogg-Dube' Syndrome (BHDS) is a rare genetic disorder in humans characterized by skin hamartomas, lung cysts, pneumothorax, and increased risk of renal tumors. BHDS is caused by mutations in the BHD gene, which encodes for Folliculin, a cytoplasmic adapter protein that binds to Folliculin...
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Bibliographic Details
| Main Authors: |
Ryan Centini,
Mark Tsang,
Terri Iwata,
Heon Park,
Jeffrey Delrow,
Daciana Margineantu,
Brandon M Iritani,
Haiwei Gu,
H Denny Liggitt,
Janella Kang,
Lim Kang,
David M Hockenbery,
Daniel Raftery,
Brian M Iritani |
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| Format: | Article
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| Language: | English |
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| Published: |
Public Library of Science (PLoS)
2018-01-01
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| Series: | PLoS ONE
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| Online Access: | https://storage.googleapis.com/plos-corpus-prod/10.1371/journal.pone.0197973/1/pone.0197973.pdf?X-Goog-Algorithm=GOOG4-RSA-SHA256&X-Goog-Credential=wombat-sa%40plos-prod.iam.gserviceaccount.com%2F20210218%2Fauto%2Fstorage%2Fgoog4_request&X-Goog-Date=20210218T051530Z&X-Goog-Expires=3600&X-Goog-SignedHeaders=host&X-Goog-Signature=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