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Artikel: Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage

Angulo, Ivan / Alain Fischer / Alison Condliffe / Andrew J. Cant / Anita Chandra / Anna Kielkowska / Anne Durandy / Capucine Picard / Changxin Wu / Christine Fiddler / Deborah Smyth / Deirdre Cilliers / Dinakantha Kumararatne / Edward Banham-Hall / Edwin R. Chilvers / Fabien Garçon / Gašper Markelj / Gabriela Barcenas-Morales / George Farmer /
Helen Baxendale / Isabelle Pellier / James A. Morris / James Curtis / Jatinder Juss / Jeffrey C. Barrett / Jonathan Clark / Katherine Blake-Palmer / Klaus Okkenhaug / Len Stephens / Mailis Maes / Marianne Debré / Mario Abinun / Menna Clatworthy / Nada Jabado / Olga Perisic / Oscar Vadas / Phillip Hawkins / Rainer Doffinger / Roger L. Williams / Sergey Nejentsev / Sven Kracker / Tanya Coulter / Timothy R. Leahy / Vincent Plagnol

Science. 2013 Nov. 15, v. 342, no. 6160

2013  

Abstract: Answers from Exomes Exome sequencing, which targets only the protein-coding regions of the genome, has the potential to identify the underlying genetic causes of rare inherited diseases. Angulo et al. (p. 866, published online 17 October; see Perspective ...

Abstract Answers from Exomes Exome sequencing, which targets only the protein-coding regions of the genome, has the potential to identify the underlying genetic causes of rare inherited diseases. Angulo et al. (p. 866, published online 17 October; see Perspective by Conley and Fruman) performed exome sequencing of individuals from seven unrelated families with severe, recurrent respiratory infections. The patients carried the same mutation in the gene coding for the catalytic subunit of phosphoinositide 3-kinase δ (PI3Kδ). The mutation caused aberrant activation of this kinase, which plays a key role in immune cell signaling. Drugs inhibiting PI3Kδ are already in clinical trials for other disorders.
Schlagwörter clinical trials ; drugs ; genes ; inheritance (genetics) ; mutation ; patients ; phosphatidylinositol 3-kinase ; protein subunits ; respiratory tract diseases ; sequence analysis
Sprache Englisch
Erscheinungsverlauf 2013-1115
Umfang p. 866-871.
Erscheinungsort American Association for the Advancement of Science
Dokumenttyp Artikel
ZDB-ID 128410-1
ISSN 1095-9203 ; 0036-8075
ISSN (online) 1095-9203
ISSN 0036-8075
DOI 10.1126/science.1243292
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Z 4' 46/137: Hefte anzeigen
+ C 27: Hefte anzeigen
Z50.00 SC01: Hefte anzeigen
Z 8.9: Hefte anzeigen
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