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The Bbsome Assembly Is Spatially Controlled by BBS1 and BBS4 in Human Cells
Near-Atomic Structures of the Bbsome Reveal a Novel Mechanism For
Ciliary Dyneins and Dynein Related Ciliopathies
Polycystin-2 Takes Different Routes to the Somatic and Ciliary Plasma Membrane
MKKS Is a Centrosome-Shuttling Protein Degraded by Disease
BBS7 Is Required for Bbsome Formation and Its Absence in Mice
Cilia and Polycystic Kidney Disease, Kith and Kin Liwei Huang* and Joshua H
BBS6, BBS10, and BBS12 Form a Complex with CCT/Tric Family Chaperonins and Mediate Bbsome Assembly
The Intraflagellar Transport Protein IFT27 Promotes Bbsome Exit
A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the Eye
Loss of the Bbsome Perturbs Endocytic Trafficking and Disrupts Virulence of Trypanosoma Brucei
Ciliary Genes in Renal Cystic Diseases
The E3 Ligase TRIM32 Is an Effector of the RAS Family Gtpase RAP2
Lysine63-Linked Ubiquitin Chains Earmark Gpcrs for Bbsome
Bardet-Biedl Syndrome: a Study of the Renal and Cardiovascular Phenotypes in a French Cohort
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
Top View
Intraflagellar Transport 27 Is Essential for Hedgehog Signaling But
Ubiquitin Chains Earmark Gpcrs for Bbsome-Mediated Removal from Cilia
Ttc8 (NM 198311) Mouse Recombinant Protein Product Data
Nuclear Roles for Cilia-Associated Proteins
Structure and Activation Mechanism of the Bbsome Membrane-Protein Trafficking Complex Sandeep Singh1, Miao Gui1, Fujiet Koh1,2, Matthew C.J
Disorders of Cilia UU
A Novel Role for Polycystin-2 (Pkd2) in P. Tetraurelia As a Probable Mg2+ Channel Necessary for Mg2+-Induced Behavior
Direct Evidence for Bbsome-Associated Intraflagellar
Intrinsic Protein-Protein Interaction-Mediated And
Developmental Disruptions Underlying Brain Abnormalities in Ciliopathies
Deletion in the Bardet–Biedl Syndrome Gene TTC8 Results in a Syndromic Retinal Degeneration in Dogs
Structure of the Human Bbsome Core Complex Bjo¨ Rn Udo Klink1, Christos Gatsogiannis1, Oliver Hofnagel1, Alfred Wittinghofer2, Stefan Raunser1*
BBS4 Regulates the Expression and Secretion of FSTL1, a Protein That
Structure of the Human Bbsome Core Complex in the Open Conformation
Altered Hematopoietic System and Self-Tolerance in Bardet-Biedl Syndrome
The Bbsome in POMC and Agrp Neurons Is Necessary for Body Weight Regulation and Sorting of Metabolic Receptors
Bardet-Biedl Syndrome Proteins Regulate Intracellular Signaling and Neuronal Function in Patient-Specific Ipsc-Derived Neurons
Biedl Syndrome
Transition Fibre Protein FBF1 Is Required for the Ciliary Entry Of
Structural Insights Into the Architecture and Assembly of Eukaryotic Flagella
Bardet–Biedl Syndrome—Multiple Kaleidoscope Images: Insight Into Mechanisms of Genotype–Phenotype Correlations