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ANK1
Human Periprostatic Adipose Tissue: Secretome from Patients With
Heterotrimeric Go Protein Links Wnt-Frizzled Signaling with Ankyrins to Regulate the Neuronal Microtubule Cytoskeleton Anne-Marie Lüchtenborg1,2, Gonzalo P
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A De Novo ANK1 Mutation Associated to Hereditary Spherocytosis: a Case Report
Review Article Mouse Homologues of Human Hereditary Disease
A Knowledge-Guided Mechanistic Model of Synthetic Lethality in The
Genetic Cardiomyopathies: the Lesson Learned from Hipscs
Cadherins As Targets for Genetic Diseases
Methylomic Profiling Implicates Cortical Deregulation of ANK1 in Alzheimer’S Disease
Human CD Marker Chart Reviewed by HLDA1 Bdbiosciences.Com/Cdmarkers
Alzheimer's Disease Risk Gene BIN1 Induces Tau-Dependent Network
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The Use of Genetic Analyses and Functional Assays for the Interpretation of Rare Variants in Pediatric Heart Disease
Clinical, Molecular, and Immune Analysis of Dabrafenib-Trametinib
Obscurin Mediates Ankyrin Complex Formation in the Heart
Defects in Cytoskeletal Signaling Pathways, Arrhythmia, and Sudden Cardiac Death
Structural Basis of Diverse Membrane Target Recognitions by Ankyrins
ANK1 Gene Ankyrin 1
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Molecular Physiology of Ankyrin-G in the Heart
ANK1 Is Up-Regulated in Laser Captured Microglia in Alzheimer’S Brain; the Importance of Addressing Cellular Heterogeneity
Alzheimer's Disease Associated Genes Ankyrin and Tau Cause
Network-Based Stratification of Tumor Mutations
There Are 1393 Genes Significant by SAM with 90Th Percentile Confidence, the False Discovery Rate Among the 1393 Significant Genes Is 0.09968
Membranes of Human Neutrophils Secretory Vesicle Membranes And
ANK1 Is Differentially Expressed in the Brains of Patients with Parkinson's Disease-PDF 080320
Alzheimer's Disease Associated Genes Ankyrin and Tau
Supporting Information
Original Article a Novel Mutation in the ANK1 Gene Causes Hereditary Spherocytosis in a Chinese Patient
Membrane Domains Based on Ankyrin and Spectrin Associated with Cell–Cell Interactions
A Cross-Brain Regions Study of ANK1 DNA Methylation in Different Neurodegenerative Diseases
Somatic Mutations
Novel Hereditary Spherocytosis-Associated Splice Site Mutation in the ANK1 Gene Caused by Parental Gonosomal Mosaicism
Novel Nonsense Mutation P. Gln264ter in the ANK1 Confirms Causative Role for Hereditary Spherocytosis: a Case Report
Significant Genes List
Diagnostic Genetic Testing Requisition
Β-III-Spectrin Spinocerebellar Ataxia Type 5 Mutation Reveals
Assembly and Dynamics of Proteins of the Longitudinal and Junctional Sarcoplasmic Reticulum in Skeletal Muscle Cells
Article Concentration (A), Mode Sizes (B) and Size Distribution Curves (C) Were Assessed by Nanoparticle Tracking Analysis
Supplement Figure 1. RAGE Impairs Regression of Non-Diabetic Atherosclerosis
The Sarcomeric Cytoskeleton: from Molecules to Motion Mathias Gautel1,* and Kristina Djinović-Carugo2,3
Insights Into the Genetics of Dilated Cardiomyopathy and Blood Cell Traits
Investigating the Biological and Molecular Consequences of Mir-9 Dysregulation In
High-Throughput Analysis of WNT Signaling Pathway in Osteoblasts
Allelic Loss and Tumor Pathology in Head and Neck Squamous Cell Carcinoma Benjamin A
Ankyrin-Based Trafficking and Scaffolding of Membrane Proteins
Regulation of Cardiac Conduction and Arrhythmias by Ankyrin/Spectrin-Based Macromolecular Complexes
Β-Catenin-Mediated Immune Evasion Pathway Frequently Operates In
NIH Public Access Author Manuscript Circulation
Argudo(2019).Pdf
Β-III-Spectrin Spinocerebellar Ataxia Type 5 Mutation Reveals a Dominant
Ankyrin-G in Skeletal Muscle: Tissue-Specific Alternative Splicing Contributes to the Complexity of the Sarcolemmal Cytoskeleton
Role of Ankyrin-B in Cardiac Function
Mis-Expression of the Alzheimer's Disease Associated Gene Ankyrin
Supplementary Table 2
Overexpression of Ankyrin1 Promotes Pancreatic Cancer Cell Growth
Genetic Diagnostics Test(S)/Gene(S)/Panel(S)