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- Bardet-Biedl Syndrome
- 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
- Cilium-Generated Signaling and Cilia-Related Disorders
- Structure and Activation Mechanism of the Bbsome Membrane-Protein Trafficking Complex Sandeep Singh1, Miao Gui1, Fujiet Koh1,2, Matthew C.J
- The Nonmotile Ciliopathies Jonathan L
- A Knockin Mouse Model of the Bardet–Biedl Syndrome 1 M390R Mutation Has Cilia Defects, Ventriculomegaly, Retinopathy, and Obesity
- STORM Imaging Reveals the Spatial Arrangement of Transition Zone Components and IFT Particles at the Ciliary Base in Tetrahymena Khodor S
- 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
- Getting to the Heart of Intraflagellar Transport Using Trypanosoma and Chlamydomonas Models: the Strength Is in Their Differences Morga and Bastin
- Next-Generation Sequencing in the Diagnosis of Patients with Bardet–Biedl Syndrome—New Variants and Relationship with Hyperglycemia and Insulin Resistance
- Bardet Biedl Syndrome
- Intraflagellar Transport Protein RABL5/IFT22 Recruits the Bbsome to the Basal Body Through the Gtpase ARL6/BBS3
- Homozygosity Mapping with SNP Arrays Identifies TRIM32, an E3 Ubiquitin Ligase, As a Bardet–Biedl Syndrome Gene (BBS11)
- EGL Test Description
- Intraflagellar Transport at a Glance Limin Hao and Jonathan M
- Developmental Disruptions Underlying Brain Abnormalities in Ciliopathies