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- The Bardet–Biedl Syndrome Protein Complex Is an Adapter Expanding
- (PKD2), Eccentric (XNTA), and Meckelin (MKS3) in the Ciliated Model Organism Paramecium Tetraurelia Megan Smith Valentine University of Vermont
- Moving Proteins Along in the Cilium
- Biedl Syndrome
- Characterization of CCDC28B Reveals Its Role in Ciliogenesis and Provides Insight to Understand Its Modifier Effect on Bardet–Biedl Syndrome
- Recurrence Risks for Bardet-Biedl Syndrome: Implications of Locus Heterogeneity Julie C
- Analysis of Six BBS Genes in a Bardet–Biedl Syndrome Family Cohort
- Further Support for Digenic Inheritance in Bardet-Biedl Syndrome S Fauser, M Munz, D Besch
- Mechanistic Insights Into Bardet-Biedl Syndrome, a Model Ciliopathy
- Structure and Activation Mechanism of the Bbsome Membrane-Protein Trafficking Complex Sandeep Singh1, Miao Gui1, Fujiet Koh1,2, Matthew C.J
- BBS1 Gene Bardet-Biedl Syndrome 1
- 0901219106SI.Pdf
- The Nonmotile Ciliopathies Jonathan L
- A Knockin Mouse Model of the Bardet–Biedl Syndrome 1 M390R Mutation Has Cilia Defects, Ventriculomegaly, Retinopathy, and Obesity
- Functional Analysis of New Human Bardet-Biedl Syndrome Loci Specific
- Intraflagellar Transport Protein RABL5/IFT22 Recruits the Bbsome to the Basal Body Through the Gtpase ARL6/BBS3
- Next-Generation Sequencing in the Diagnosis of Patients with Bardet–Biedl Syndrome—New Variants and Relationship with Hyperglycemia and Insulin Resistance
- Direct Evidence for Bbsome-Associated Intraflagellar