Identification of Functional Variants in the FAM13A Chronic Obstructive Pulmonary Disease Genome-Wide Association Study Locus by Massively Parallel Reporter Assays-Reference-Cited by-同舟云学术

Identification of Functional Variants in the FAM13A Chronic Obstructive Pulmonary Disease Genome-Wide Association Study Locus by Massively Parallel Reporter Assays

Published:2019-01 Issue:1 Volume:199 Page:52-61
ISSN:1073-449X
Container-title:American Journal of Respiratory and Critical Care Medicine
language:en
Short-container-title:Am J Respir Crit Care Med

Author:

Castaldi Peter J.¹²,Guo Feng¹,Qiao Dandi¹,Du Fei¹,Naing Zun Zar Chi¹,Li Yan¹,Pham Betty¹,Mikkelsen Tarjei S.³,Cho Michael H.¹²,Silverman Edwin K.¹²,Zhou Xiaobo¹²^ORCID

Affiliation:

1. Channing Division of Network Medicine and

2. Division of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School, Boston, Massachusetts; and

3. Broad Institute, Cambridge, Massachusetts

Publisher

American Thoracic Society

Subject

Critical Care and Intensive Care Medicine,Pulmonary and Respiratory Medicine

Link

https://www.atsjournals.org/doi/pdf/10.1164/rccm.201802-0337OC

Reference28 articles.

1. Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis

2. Identification of a chronic obstructive pulmonary disease genetic determinant that regulates HHIP

3. The G82S Polymorphism Promotes Glycosylation of the Receptor for Advanced Glycation End Products (RAGE) at Asparagine 81

4. Variants in FAM13A are associated with chronic obstructive pulmonary disease

5. Reduced Frizzled Receptor 4 Expression Prevents WNT/β-Catenin–driven Alveolar Lung Repair in Chronic Obstructive Pulmonary Disease

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