Ciliopathy is differentially distributed in the brain of a Bardet-Biedl syndrome mouse model.
Bardet-Biedl syndrome (BBS) is a genetically heterogeneous inherited human disorder displaying a pleotropic phenotype. Many of the symptoms characterized in the human disease have been reproduced in animal models carrying deletions or knock-in mutations of genes causal for the disorder. Thinning of...
Saved in:
| Main Authors: | Khristofor Agassandian, Milan Patel, Marianna Agassandian, Karina E Steren, Kamal Rahmouni, Val C Sheffield, J Patrick Card |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2014-01-01
|
| Series: | PLoS ONE |
| Online Access: | https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0093484&type=printable |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Recurrent Nasal Polyposis and Bifid Epiglottis in a Child with Bardet–Biedl Syndrome Ciliopathy
by: Natalia Fourla, et al.
Published: (2024-11-01) -
Bardet–Biedl syndrome
by: Shrinkhal, et al.
Published: (2025-07-01) -
Manifestations of Bardet-Biedl syndrome
by: Kristine T. Lo, MD, et al.
Published: (2004-06-01) -
Sudden acquired retinal degeneration syndrome may be an acquired primary ciliopathy, phenotypically similar to human Alström and Bardet-Biedl syndromes
by: Steven Toler, et al.
Published: (2025-06-01) -
Bangladeshi Case Series of Bardet–Biedl Syndrome
by: Fariah Osman, et al.
Published: (2023-01-01)