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Cyclin-Dependent Kinase (CDK) Inhibitors

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Cover of 'Cyclin-Dependent Kinase (CDK) Inhibitors'

Table of Contents

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    Book Overview
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    Chapter 1 Cyclin-Dependent Kinase (CDK) Inhibitors
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    Chapter 2 Expression and Purification of Recombinant Cyclins and CDKs for Activity Evaluation
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    Chapter 3 Expression and Purification of Recombinant CDKs: CDK7, CDK8, and CDK9
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    Chapter 4 Preparation of CDK/Cyclin Inhibitor Complexes for Structural Determination
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    Chapter 5 Fragment-Based De Novo Design of Cyclin-Dependent Kinase 2 Inhibitors
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    Chapter 6 Protein-Protein Interaction for the De Novo Design of Cyclin-Dependent Kinase Peptide Inhibitors
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    Chapter 7 Identification of Cyclin A Binders with a Fluorescent Peptide Sensor
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    Chapter 8 Cyclin-Dependent Kinase (CDK) Inhibitors
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    Chapter 9 Analysis of CDK Inhibitor Action on Mitochondria-Mediated Apoptosis
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    Chapter 10 Evaluating the Effects of CDK Inhibitors in Ischemia–Reperfusion Injury Models
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    Chapter 11 Assessing Cell Cycle Independent Function of the CDK Inhibitor p21(CDKN1A) in DNA Repair.
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    Chapter 12 Drug Delivery Strategies of Chemical CDK Inhibitors
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    Chapter 13 Animal Models for Studying the In Vivo Functions of Cell Cycle CDKs.
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    Chapter 14 Evaluating Chemical CDK Inhibitors as Cell Death Inducers
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    Chapter 15 Models for the Study of the Cross Talk Between Inflammation and Cell Cycle
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    Chapter 16 Metabolomic Applications to the Characterization of the Mode-of-Action of CDK Inhibitors
Attention for Chapter 10: Evaluating the Effects of CDK Inhibitors in Ischemia–Reperfusion Injury Models
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Chapter title
Evaluating the Effects of CDK Inhibitors in Ischemia–Reperfusion Injury Models
Chapter number 10
Book title
Cyclin-Dependent Kinase (CDK) Inhibitors
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-2926-9_10
Pubmed ID
Book ISBNs
978-1-4939-2925-2, 978-1-4939-2926-9
Authors

Tatiana Guevara

Abstract

CDK inhibitors have been used to induce protection in various experimental models. Kidney ischemia-reperfusion (I/R) is a form of acute kidney injury resulting in a cascade of cellular events prompting rapid cellular damage and suppression of kidney function. I/R injury, an inevitable impairment during renal transplant surgery, remains one of the major causes of acute kidney injury and represents the most prominent factor leading to delayed graft function after transplantation. Understanding the molecular events responsible for tubule damage and recovery would help to develop new strategies for organ preservation. This chapter describes procedures to study the effect of CDK inhibitors in the cellular I/R model developed from an epithelial cell line deriving from pig kidney proximal tubule cells (LLC-PK1). We briefly describe methods for determining the protective effect of CDK inhibitors such as activation of caspase 3/7, western blot analysis, gene silencing, and immunoprecipitation.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 1 20%
Student > Ph. D. Student 1 20%
Researcher 1 20%
Unknown 2 40%
Readers by discipline Count As %
Unspecified 1 20%
Pharmacology, Toxicology and Pharmaceutical Science 1 20%
Engineering 1 20%
Unknown 2 40%