Functional Characterization of Mutations in Inherited Human cPLA2 Deficiency-Reference-Cited by-同舟云学术

Functional Characterization of Mutations in Inherited Human cPLA2 Deficiency

Published:2011-02-09 Issue:10 Volume:50 Page:1731-1738
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Reed Kathleen A.¹,Tucker Dawn E.²,Aloulou Ahmed³,Adler David¹,Ghomashchi Farideh³,Gelb Michael H.³,Leslie Christina C.²⁴,Oates John A.¹⁵,Boutaud Olivier⁵

Affiliation:

1. Department of Medicine

2. Department of Pediatrics, National Jewish Health, Denver, Colorado 80206, United States

3. Departments of Chemistry and Biochemistry, University of Washington, Seattle, Washington 98195, United States

4. Departments of Pathology and Pharmacology, University of Colorado Denver, Aurora, Colorado 80045, United States

5. Department of Pharmacology

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi101877n

Reference21 articles.

1. Role of cytosolic phospholipase A2 in allergic response and parturition

2. Reduced fertility and postischaemic brain injury in mice deficient in cytosolic phospholipase A2

3. Properties of the Group IV phospholipase A2 family

4. Delineation of two functionally distinct domains of cytosolic phospholipase A2, a regulatory Ca(2+)-dependent lipid-binding domain and a Ca(2+)-independent catalytic domain.

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