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INPP5E
Regulation of Phosphoinositide Levels in the Retina by Protein Tyrosine Phosphatase 1B and Growth Factor Receptor-Bound Protein 14
The Role of Genetic Variation in Predisposition to Alcohol-Related Chronic Pancreatitis
Whole Exome Sequencing Analyses Reveal Gene–Microbiota Interactions
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Epigenomic Signatures in Liver and Blood of Wilson Disease Patients Include Hypermethylation of Liver‑Specifc Enhancers Charles E
A Transient Role of the Ciliary Gene Inpp5e in Controlling Direct Versus
The Dual Roles of Betacellulin and the ERBB Receptors in Acute Pancreatitis & Pancreatic Ductal Adenocarcinoma – a Mouse Study
ARL13B, PDE6D, and CEP164 Form a Functional Network for INPP5E Ciliary Targeting
Downloaded October, 2015) 83
Live-Cell Imaging Rnai Screen Identifies PP2A–B55α and Importin-Β1 As Key Mitotic Exit Regulators in Human Cells
Mediated Sorting of INPP5E Into the Cilium Is Determined by Cargo-Carrier Affinity
Phosphatases Page 1
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
Supplemental Figures 04 12 2017
Roles in Axon Regeneration and Synaptogenesis
INPP5E Interacts with AURKA, Linking Phosphoinositide Signaling To
INPP5E Controls Ciliary Localization of Phospholipids and the Odor
Heterozygous Inactivation of the Na/Ca Exchanger Increases
Top View
Synovial Fluid Proteome in Rheumatoid Arthritis
Generate Metabolic Map Poster
Regulation of Ciliary Retrograde Protein Trafficking by the Joubert Syndrome
The Joubert Syndrome Protein Inpp5e Controls Ciliogenesis by Regulating Phosphoinositides at the Apical Membrane
1 Imipramine Treatment and Resiliency Exhibit Similar
Differentially Expressed Mirnas Influence Metabolic Processes In
DEVELOPMENTAL BIOLOGY 2 Antibodies for Developmental Biology
Somatic Mutations
Inositol Polyphosphate 5-Phosphatases; New Players in the Regulation of Cilia and Ciliopathies ⇑ Sarah E
The Ciliary Phosphatidylinositol Phosphatase Inpp5e Plays Positive and Negative Regulatory Roles in Shh Signaling Sandii Constable*,1, Alyssa B
Phenotypic Spectrum and Prevalence of INPP5E Mutations in Joubert Syndrome and Related Disorders
A Phosphoinositide Conversion Mechanism for Exit from Endosomes
Binding to SLP65 Mediated − 2 Via C2 Domain Γ Phospholipase C Cutting Edge: Feed-Forward Activation Of
Metabolske Sykdommer V02
Generated by SRI International Pathway Tools Version 25.0 on Mon
A Structure of Substrate-Bound Synaptojanin1 Provides New Insights in Its Mechanism and the Effect of Disease Mutations
TFEB Regulates Lysosomal Positioning by Modulating TMEM55B Expression and JIP4 Recruitment to Lysosomes
Anti-INPP5E (Full Length) Polyclonal Antibody (CABT-BL4927) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
1 Identification of Protein-Protected Mrna Fragments and Structured
The Ciliary Gene INPP5E Confers Dorsal Telencephalic Identity to Human Cortical Organoids by Negatively Regulating Sonic Hedgehog Signalling
Supplementary Table 1; List of Analyzed Genes
Identification of Protein-Protected Mrna Fragments and Structured
Cell Signalling Pathways 2 1
Early Onset Non-Syndromic Retinal Degeneration Due to Variants in INPP5E: Phenotypic
Supplemental Material
Cell Signalling Pathways 2 1
The Major Ciliary Isoforms of RPGR Build Different Interaction Complexes with INPP5E and RPGRIP1L
Mutant Plasticity Related Gene 1 (PRG1) Acts As a Potential Modifier in SCN1A Related Epilepsy
Generated by SRI International Pathway Tools Version 24.0 on Thu