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BBS9
Near-Atomic Structures of the Bbsome Reveal the Basis for Bbsome
Ciliopathiesneuromuscularciliopathies Disorders Disorders Ciliopathiesciliopathies
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity Received: 11 November 2016 Audrey E
Ciliopathies Gene Panel
BBS1 Is Involved in Retrograde Trafficking of Ciliary Gpcrs in the Context of the Bbsome Complex
Myopia in African Americans Is Significantly Linked to Chromosome 7P15.2-14.2
Nonsyndromic Craniosynostosis
BBS6, BBS10, and BBS12 Form a Complex with CCT/Tric Family Chaperonins and Mediate Bbsome Assembly
Whole-Exome Sequencing Identifies Causative Mutations in Families
BBS6, BBS10, and BBS12 Form a Complex with CCT/Tric Family Chaperonins and Mediate Bbsome Assembly
Ciliary Genes in Renal Cystic Diseases
Identification of a Novel Homozygous Missense (C. 443A> T: P. N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome
Panel-Based Next Generation Sequencing As a Reliable and Efficient Technique to Detect Mutations in Unselected Patients With
Next Generation Sequencing Identifies Five Novel Mutations In
(PKD2), Eccentric (XNTA), and Meckelin (MKS3) in the Ciliated Model Organism Paramecium Tetraurelia Megan Smith Valentine University of Vermont
Ciliopathies
UCSC Hg19 Coordinate Chromosome Start End Gene Chr1 94458393
Evolution of Modular Intraflagellar Transport from a Coatomer-Like
Top View
Bardet–Biedl Syndrome: Beyond the Cilium
Of the BBS9 Gene in a Consanguineous Paki
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Ftm Is a Novel Basal Body Protein of Cilia Involved in Shh Signalling
Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani Families
Chapter 4: Role of Modifier Effects on Retinal Phenotypes In
From Sequence to Phenotype: the Impact of Deleterious Variation in Livestock
Structure and Activation Mechanism of the Bbsome Membrane-Protein Trafficking Complex Sandeep Singh1, Miao Gui1, Fujiet Koh1,2, Matthew C.J
Structure of the Yeast Swi/Snf Complex in a Nucleosome Free State
STORM Imaging Reveals the Spatial Arrangement of Transition Zone Components and IFT Particles at the Ciliary Base in Tetrahymena Khodor S
Ciliopathies Gene Panel
Weighted Gene Coexpression Network Analysis Strategies Applied to Mouse Weight
Next-Generation Sequencing in the Diagnosis of Patients with Bardet–Biedl Syndrome—New Variants and Relationship with Hyperglycemia and Insulin Resistance
June 2013 Preventiongenetics Newsletter
Bardet Biedl Syndrome
Intrinsic Protein-Protein Interaction-Mediated And
Requirement of IFT-B–Bbsome Complex Interaction in Export of GPR161 from Cilia Shohei Nozaki, Roiner Francisco Castro Araya, Yohei Katoh* and Kazuhisa Nakayama*
Cone Rod Dystrophy Precision Panel Overview Indications Clinical Utility