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BBS7
Invited Review: Genetic and Genomic Mouse Models for Livestock Research
Supporting Information
Knockdown of the BBS10 Gene Product
Transmission Distortion and Genetic Incompatibilities Between Alleles in A
BBS7 Is Required for Bbsome Formation and Its Absence in Mice
BBS6, BBS10, and BBS12 Form a Complex with CCT/Tric Family Chaperonins and Mediate Bbsome Assembly
UC San Francisco Previously Published Works
Microrna-124-3P Suppresses Mouse Lip Mesenchymal Cell Proliferation
Defects and Compromised Intraflagellar Transport BBS-7 and BBS-8 Protein Function Results in Cilia C. Elegans Loss Of
BBS6, BBS10, and BBS12 Form a Complex with CCT/Tric Family Chaperonins and Mediate Bbsome Assembly
Ciliary Genes in Renal Cystic Diseases
Targeted High-Throughput Sequencing for Diagnosis of Genetically Heterogeneous Diseases: Efficient Mutation Detection in Bardet
Next Generation Sequencing Identifies Five Novel Mutations In
Bardet-Biedl Syndrome: a Study of the Renal and Cardiovascular Phenotypes in a French Cohort
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
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
BBS7 Rabbit Pab
Top View
Gnomad Lof Supplement
Genetic Testing for Developmental Disabilities, Intellectual Disability, and Autism Spectrum Disorder Technical Brief Number 23
Carrier Frequency of Two BBS2 Mutations in the Ashkenazi Population
Further Support for Digenic Inheritance in Bardet-Biedl Syndrome S Fauser, M Munz, D Besch
Cilium-Generated Signaling and Cilia-Related Disorders
Locus Heterogeneity Disease Genes Encode Proteins with High Interconnectivity in the Human Protein Interaction Network
Next-Generation Sequencing in the Diagnosis of Patients with Bardet–Biedl Syndrome—New Variants and Relationship with Hyperglycemia and Insulin Resistance
Genotype-Phenotype Correlations in Bardet-Biedl Syndrome
Gene Expression Atlas of Energy Balance Brain Regions
Intrinsic Protein-Protein Interaction-Mediated And
1 Gene Expression Atlas of Energy Balance Brain Regions Maria
Developmental Disruptions Underlying Brain Abnormalities in Ciliopathies
PDF Hosted at the Radboud Repository of the Radboud University Nijmegen
Downloaded from Placed in a Duplication Node More Closely Related to the the Gene Ontology’S Archive of MGI Gafs [52]
Structure of the Human Bbsome Core Complex in the Open Conformation
Defining the Molecular Mechanisms of Cep290 Disease Pathogenesis
Direct Role of Bardet–Biedl Syndrome Proteins in Transcriptional Regulation
Bardet-Biedl Syndrome Proteins Regulate Intracellular Signaling and Neuronal Function in Patient-Specific Ipsc-Derived Neurons