Cerebral Cavernous Malformations (CCM) Methods and Protocols /

書目詳細資料
企業作者: SpringerLink (Online service)
其他作者: Trabalzini, Lorenza (Editor), Finetti, Federica (Editor), Retta, Saverio Francesco (Editor)
總結:XV, 496 p. 86 illus., 62 illus. in color.
text
語言:英语
出版: New York, NY : Springer US : Imprint: Humana, 2020.
版:1st ed. 2020.
叢編:Methods in Molecular Biology, 2152
主題:
在線閱讀:https://doi.org/10.1007/978-1-0716-0640-7
格式: 電子 電子書
書本目錄:
  • From Genes and Mechanisms to Molecular-targeted Therapies: the Long Climb to the Cure of Cerebral Cavernous Malformation (CCM) Disease
  • Incidence, Prevalence, and Clinical Presentation of Cerebral Cavernous Malformations
  • Natural History, Clinical, and Surgical Management of Cavernous Malformations
  • Molecular Genetics Screening of CCM patients, An Overview
  • Next Generation Sequecing (NGS) Strategies for Genetic Testing and Diagnosis of Cerebral Cavernous Malformation (CCM) Disease
  • Genome-wide Genotyping of Cerebral Cavernous Malformation Type 1 Individuals to Identify Genetic Modifiers of Disease Severity
  • Clinical Imaging of Cerebral Cavernous Malformations: Computed Tomography and Magnetic Resonance Imaging
  • Neuroradiology: Differential Diagnosis, Follow-Up, and Reporting
  • Surgical Management of Brain Cavernous Malformations
  • Generation of CCM Phenotype by a Human Microvascular Endothelial Model
  • Isolation and Purification of Mouse Brain Endothelial Cells to Study Cerebral Cavernous Malformation Disease
  • Production of KRIT1-knockout and KRIT1-knockin Mouse Embryonic Fibroblasts as Cellular Models of CCM Disease
  • CRISPR/Cas9-mediated Generation of Human Endothelial Cell Knockout Models of CCM Disease
  • Dissection of the Role of CCM Genes in Tubulogenesis using the Drosophila Tracheal System as a Model
  • Generation and Analysis of CCM Phenotypes in C. elegans
  • Generation of Transgenic Lines of Zebrafish Expressing Fluorescently-tagged CCM Proteins to Study Their Function and Subcellular Localization within the Vasculature
  • Vertebrate Models to Investigate CCM Pathogenesis: The Zebrafish and Mouse Model
  • Generation of Cerebral Cavernous Malformation in Neonatal Mouse Models using Inducible Cre-LoxP Strategy
  • Isolation of Cerebral Endothelial Cells from CCM1/KRIT1 Null Mouse Brain
  • Identification of the KRIT1 Protein by LexA-based Yeast Two-Hybrid System
  • Crystallographic Studies of the Cerebral Cavernous Malformations Proteins
  • Microscopy Techniques to Investigate CCM Pathogenesis
  • Preparation and Analysis of Protein Extracts to Investigate CCM Pathogenesis
  • Systems Wide Analysis of CCM Signaling Complex (CSC) Alterations in CCM Deficient Models using Omics Approaches
  • Study of Molecular Interactions of CCM Proteins by using a GAL4-based Yeast Two-hybrid Screening
  • Study of CCM Microvascular Endothelial Phenotype by an in vitro Tubule Differentiation Model
  • Bidimentional in vitro Angiogenic Assays to Study CCM Pathogenesis: Endothelial Cell Proliferation and Migration
  • Measurement of Endothelial Barrier Function in Mouse Models of Cerebral Cavernous Malformations using Intravital Microscopy
  • Immunofluorescence of Cell-Cell and Cell-Extracellular Matrix Adhesive Defects in in vitro Endothelial CCM Model. Juxtacrine Role of Mutant Extracellular Matrix on Wild-Type Endothelial Cells
  • Detection of p62/SQSTM1Aggregates in Cellular Models of CCM Disease by Immunofluorescence
  • Notch Signaling in Familial Cerebral Cavernous Malformations and Immunohistochemical Detection of cleaved Notch1 Intracellular Domain
  • Measuring the Kinase Activity of GCKIII Proteins in vitro
  • Spectrophotometric Method for Determining Glyoxalase 1 Activity in Cerebral Cavernous Malformation (CCM) Disease
  • Fluorescence Analysis of Reactive Oxygen Species (ROS) in Cellular Models of Cerebral Cavernous Malformation Disease
  • Small RNA Library Preparation for Profiling Small Non-coding RNAs in Patients Affected by Cavernous Malformations
  • Affinity Purification and Preparation of Peptides for Mass Spectrometry from C. elegans. .