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IFT80
Educational Paper Ciliopathies
Ciliopathiesneuromuscularciliopathies Disorders Disorders Ciliopathiesciliopathies
Ciliopathies Gene Panel
20140826 Supplementary Material FINAL
Cldn19 Clic2 Clmp Cln3
Composition and Function of the C1b/C1f Region in the Ciliary Central
Cilia-Related Protein SPEF2 Regulates Osteoblast Differentiation
Whole-Exome Sequencing Identifies Causative Mutations in Families
Targeted Sequence Capture and Ultra High Throughput Sequencing for Gene Discovery in Inherited Diseases
Cystic Kidney Diseases and During Vertebrate Gastrulation
Genetic Basis for Congenital Heart Disease: Revisited a Scientific Statement from the American Heart Association Endorsed by the American Academy of Pediatrics
IFT80 Gene Intraflagellar Transport 80
Bardet-Biedl Syndrome
Dampened Hedgehog Signaling but Normal Wnt Signaling in Zebrafish Without Cilia Peng Huang* and Alexander F
EGL Test Description
Mutations in CCDC39 and CCDC40 Are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Asphyxiating Thoracic Dystrophy
Top View
IFT80 Improves Invasion Ability in Gastric Cancer Cell Line Via Ift80/P75ngfr/MMP9 Signaling
Supplementary Tables 1-18 Contain the Predictive Signatures Determined for Each AML Subgroup Using Prediction Analysis for Microarrays (PAM)
Ciliopathies
Table S1. Candidate Genes for the Phenotypes Polydactyly, Syndactyly and Polysyndactyly in Domestic Animals According to NCBI and OMIA
Clinical and Genetic Aspects of Primary Ciliary Dyskinesia/Kartagener Syndrome Margaret W
A Systems-Biology Approach to Understanding the Ciliopathy Disorders Ji Eun Lee and Joseph G Gleeson*
The Importance of Genomic Profiling for Differential Diagnosis of Pediatric
Kidneyseq™ V4 – 312 Genes CAKUT Branchiooculofacial Syndrome AD
Crystal Structure of Intraflagellar Transport Protein 80 Reveals a Homo
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
Primary Cilia Control Hedgehog Signaling During Muscle Differentiation and Are Deregulated in Rhabdomyosarcoma
Regulation of Ciliary Retrograde Protein Trafficking by the Joubert Syndrome
0901219106SI.Pdf
An Overview of in Vivo and in Vitro Models for Autosomal Dominant Polycystic Kidney Disease: a Journey from 3D-Cysts to Mini-Pigs
Ciliary IFT80 Balances Canonical Versus Non-Canonical Hedgehog Signalling for Osteoblast Differentiation
Supplemental Data
Ciliary IFT80 Balances Canonical Versus Non-Canonical Hedgehog Signalling for Osteoblast Differentiation
Arl13b Regulates Breast Cancer Cell Migration and Invasion by Controlling Integrin-Mediated Signaling
Ciliopathies Gene Panel
NIH Public Access Author Manuscript Hum Mutat
EGL Test Description
Newborndxtm Advanced Sequencing Evaluation Disorders List
Requirement of IFT-B–Bbsome Complex Interaction in Export of GPR161 from Cilia Shohei Nozaki, Roiner Francisco Castro Araya, Yohei Katoh* and Kazuhisa Nakayama*
Retinal Disease in Ciliopathies: Recent Advances with a Focus on Stem Cell-Based Therapies
Developmental Disruptions Underlying Brain Abnormalities in Ciliopathies
Downloaded from Placed in a Duplication Node More Closely Related to the the Gene Ontology’S Archive of MGI Gafs [52]
Co-Occurrence of Joubert Syndrome and Jeune Asphyxiating Thoracic Dystrophy A.M
ABSTRACT Gene Expression Profiling to Understand the Alterations In
The Intraflagellar Transport Machinery
Truncation of IFT80 Causes Early Embryonic Loss in Cattle
STAT Autism and Intellectual Disability Panel
The Intraflagellar Transport Protein IFT57 Is Required for Cilia Maintenance and Regulates IFT-Particle– Kinesin-II Dissociation in Vertebrate Photoreceptors
Modeling Microcephaly Caused by Inactivation of the Minor
Synergistic Genetic Interactions Between Pkhd1 and Pkd1 Result in an ARPKD-Like Phenotype in Murine Models
Cilia Interactome with Predicted Protein–Protein Interactions Reveals Connections to Alzheimer’S Disease, Aging and Other Neuropsychiatric Processes Kalyani B
Snapshot: Intraflagellar Transport Douglas G
Intraflagellar Transport Proteins 172, 80, 57, 54, 38, 
Biedl Syndrome (BBS) in CEP76