Jordan K Abbott
Overview
Explore the profile of Jordan K Abbott including associated specialties, affiliations and a list of published articles.
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24
Citations
652
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Recent Articles
11.
Hui J, Banks M, Nadasdy T, Rovin B, Abbott J
Kidney Int Rep
. 2020 Jun;
5(6):951-954.
PMID: 32518880
No abstract available.
12.
Wang M, Strand M, Lanser B, Santos C, Bendelja K, Fish J, et al.
PLoS One
. 2020 Jun;
15(6):e0233563.
PMID: 32497050
Activation of the steroidogenic enzyme CYP11A1 was shown to be necessary for the development of peanut-induced intestinal anaphylaxis and IL-13 production in allergic mice. We determined if levels of CYP11A1...
13.
Meyer A, Banks M, Nadasdy T, Clark J, Zheng R, Gelfand E, et al.
Front Pediatr
. 2019 Nov;
7:390.
PMID: 31709200
A subset of patients with Ataxia-Telangiectasia (A-T) have dramatically reduced levels of IgG, IgA, and IgE with retained or elevated IgM levels. Several reports suggest that these A-T patients with...
14.
Bosticardo M, Yamazaki Y, Cowan J, Giardino G, Corsino C, Scalia G, et al.
Am J Hum Genet
. 2019 Aug;
105(3):549-561.
PMID: 31447097
FOXN1 is the master regulatory gene of thymic epithelium development. FOXN1 deficiency leads to thymic aplasia, alopecia, and nail dystrophy, accounting for the nude/severe combined immunodeficiency (nu/SCID) phenotype in humans...
15.
Maffucci P, Chavez J, Jurkiw T, OBrien P, Abbott J, Reynolds P, et al.
J Clin Invest
. 2018 Nov;
128(12):5489-5504.
PMID: 30395541
We report the molecular, cellular, and clinical features of 5 patients from 3 kindreds with biallelic mutations in the autosomal LIG1 gene encoding DNA ligase 1. The patients exhibited hypogammaglobulinemia,...
16.
Abbott J, Huoh Y, Reynolds P, Yu L, Rewers M, Reddy M, et al.
J Autoimmun
. 2017 Nov;
88:114-120.
PMID: 29129473
A genetic variant in the SAND domain of autoimmune regulator (AIRE), R247C, was identified in a patient with type I diabetes mellitus (T1DM) and his mother with rheumatoid arthritis. In ...
17.
Ma C, Stinson J, Zhang Y, Abbott J, Weinreich M, Hauk P, et al.
Nat Genet
. 2017 Oct;
49(11):1661.
PMID: 29074947
This corrects the article DOI: 10.1038/ng.3898.
18.
Ma C, Stinson J, Zhang Y, Abbott J, Weinreich M, Hauk P, et al.
Nat Genet
. 2017 Jun;
49(8):1192-1201.
PMID: 28628108
Few monogenic causes for severe manifestations of common allergic diseases have been identified. Through next-generation sequencing on a cohort of patients with severe atopic dermatitis with and without comorbid infections,...
19.
Lamborn I, Jing H, Zhang Y, Drutman S, Abbott J, Munir S, et al.
J Exp Med
. 2017 Jun;
214(7):1949-1972.
PMID: 28606988
MDA5 is a cytosolic sensor of double-stranded RNA (ds)RNA including viral byproducts and intermediates. We studied a child with life-threatening, recurrent respiratory tract infections, caused by viruses including human rhinovirus...
20.
de la Morena M, Leonard D, Torgerson T, Cabral-Marques O, Slatter M, Aghamohammadi A, et al.
J Allergy Clin Immunol
. 2016 Oct;
139(4):1282-1292.
PMID: 27697500
Background: X-linked hyper-IgM syndrome (XHIGM) is a primary immunodeficiency with high morbidity and mortality compared with those seen in healthy subjects. Hematopoietic cell transplantation (HCT) has been considered a curative...