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NF-κB-Related Genetic Diseases
~
Ursini, Matilde Valeria.
NF-κB-Related Genetic Diseases
Record Type:
Language materials, printed : Monograph/item
Title/Author:
NF-κB-Related Genetic Diseases/ by Gilles Courtois, Alessandra Pescatore, Jérémie Gautheron, Francesca Fusco, Matilde Valeria Ursini, Anna Senegas.
Author:
Courtois, Gilles.
other author:
Pescatore, Alessandra.
Description:
XII, 70 p. 17 illus.online resource. :
Contained By:
Springer Nature eBook
Subject:
Human genetics. -
Online resource:
https://doi.org/10.1007/978-3-319-25850-8
ISBN:
9783319258508
NF-κB-Related Genetic Diseases
Courtois, Gilles.
NF-κB-Related Genetic Diseases
[electronic resource] /by Gilles Courtois, Alessandra Pescatore, Jérémie Gautheron, Francesca Fusco, Matilde Valeria Ursini, Anna Senegas. - 1st ed. 2016. - XII, 70 p. 17 illus.online resource. - SpringerBriefs in Biochemistry and Molecular Biology,2211-9353. - SpringerBriefs in Biochemistry and Molecular Biology,.
1) The NF-kB signaling pathways: players and Functions -- 2) Genetic Diseases Affecting the Canonical Pathway of NF-kB Activation -- 3) Genetic Diseases Affecting hte Non-Camonical Pathway of NF-kB Activation -- 4) Genetic Diseases Affecting Ubiquitination Processes in NF-kB Signaling -- 5)Lessons Learned from Studying NF-kB Related Genetic Diseases.
This book presents the diverse clinical, cellular and molecular manifestations of NF-KB-related genetic diseases. It shows that studying patient-related pathologies affecting the components of the NF-KB signaling pathway offers the opportunity to understand the various functions of NF-KB in humans, complementing studies performed with mouse models. In addition, people treating those patients acquire a deeper understanding of the molecular basis of the pathophysiological processes.
ISBN: 9783319258508
Standard No.: 10.1007/978-3-319-25850-8doiSubjects--Topical Terms:
596505
Human genetics.
LC Class. No.: QH506
Dewey Class. No.: 611.01816
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This book presents the diverse clinical, cellular and molecular manifestations of NF-KB-related genetic diseases. It shows that studying patient-related pathologies affecting the components of the NF-KB signaling pathway offers the opportunity to understand the various functions of NF-KB in humans, complementing studies performed with mouse models. In addition, people treating those patients acquire a deeper understanding of the molecular basis of the pathophysiological processes.
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