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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 2: Expression and Purification of Recombinant Cyclins and CDKs for Activity Evaluation
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Chapter title
Expression and Purification of Recombinant Cyclins and CDKs for Activity Evaluation
Chapter number 2
Book title
Cyclin-Dependent Kinase (CDK) Inhibitors
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-2926-9_2
Pubmed ID
Book ISBNs
978-1-4939-2925-2, 978-1-4939-2926-9
Authors

Edurne Gallastegui, Oriol Bachs

Abstract

Cyclin-dependent kinases (Cdks) belong to a family of key regulators of cell division cycle and transcription. Their activity is mainly regulated by association with regulatory subunits named cyclins but their activities are also regulated by phosphorylation, acetylation, and the association with specific inhibitory proteins (CKIs). The activity of different Cdks is deregulated in many different type of tumors, and thus, Cdks are considered targets for antitumoral therapy. For large screenings of inhibitors the use of purified recombinant Cdks and cyclins is recommended. We report here the current methods to determine their in vitro activity for large screenings of inhibitors.

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Mendeley readers

The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Unspecified 1 33%
Student > Ph. D. Student 1 33%
Unknown 1 33%
Readers by discipline Count As %
Unspecified 1 33%
Biochemistry, Genetics and Molecular Biology 1 33%
Unknown 1 33%