Jason C Collins
Overview
Explore the profile of Jason C Collins including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
546
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0
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Recent Articles
1.
Collins J, Magaziner S, English M, Hassan B, Chen X, Balanda N, et al.
EMBO J
. 2024 Feb;
43(10):1919-1946.
PMID: 38360993
Most cellular ubiquitin signaling is initiated by UBA1, which activates and transfers ubiquitin to tens of E2 enzymes. Clonally acquired UBA1 missense mutations cause an inflammatory-hematologic overlap disease called VEXAS...
2.
Collins J, Magaziner S, English M, Hassan B, Chen X, Balanda N, et al.
bioRxiv
. 2023 Oct;
PMID: 37873213
Most cellular ubiquitin signaling is initiated by UBA1, which activates and transfers ubiquitin to tens of E2 enzymes. Clonally acquired missense mutations cause an inflammatory-hematologic overlap disease called VEXAS (vacuoles,...
3.
Asmar A, Abrams S, Hsin J, Collins J, Yazejian R, Wu Y, et al.
Nat Commun
. 2023 Jul;
14(1):4499.
PMID: 37495603
The molecular mechanisms that coordinate patterning of the embryonic ectoderm into spatially distinct lineages to form the nervous system, epidermis, and neural crest-derived craniofacial structures are unclear. Here, biochemical disease-variant...
4.
Stiburkova B, Pavelcova K, Belickova M, Magaziner S, Collins J, Werner A, et al.
Arthritis Rheumatol
. 2023 Feb;
75(7):1285-1290.
PMID: 36762418
Objective: Somatic mutations in UBA1 have recently been causally linked to a severe adult-onset inflammatory condition referred to as VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome. Ubiquitin-activating enzyme E1...
5.
Ferrada M, Savic S, Ospina Cardona D, Collins J, Alessi H, Gutierrez-Rodrigues F, et al.
Blood
. 2022 Jul;
140(13):1496-1506.
PMID: 35793467
Somatic mutations in UBA1 cause vacuoles, E1 ubiquitin-activating enzyme, X-linked, autoinflammatory somatic (VEXAS) syndrome, an adult-onset inflammatory disease with an overlap of hematologic manifestations. VEXAS syndrome is characterized by a...
6.
Chatrathi H, Collins J, Wolfe L, Markello T, Adams D, Gahl W, et al.
Hypertension
. 2021 Dec;
79(1):60-75.
PMID: 34878901
Familial hyperkalemic hypertension is caused by pathogenic variants in genes of the CUL3 (cullin-3)-KLHL3 (kelch-like-family-member-3)-WNK (with no-lysine [K] kinase) pathway, manifesting clinically as hyperkalemia, metabolic acidosis, and high systolic blood...
7.
Poulter J, Collins J, Cargo C, De Tute R, Evans P, Ospina Cardona D, et al.
Blood
. 2021 Mar;
137(26):3676-3681.
PMID: 33690815
No abstract available.
8.
Beck D, Ferrada M, Sikora K, Ombrello A, Collins J, Pei W, et al.
N Engl J Med
. 2020 Oct;
383(27):2628-2638.
PMID: 33108101
Background: Adult-onset inflammatory syndromes often manifest with overlapping clinical features. Variants in ubiquitin-related genes, previously implicated in autoinflammatory disease, may define new disorders. Methods: We analyzed peripheral-blood exome sequence data...
9.
Parker M, Collins J, Korona B, Ghalei H, Karbstein K
PLoS Biol
. 2020 Oct;
18(10):e3000960.
PMID: 33048931
[This corrects the article DOI: 10.1371/journal.pbio.3000329.].
10.
Parker M, Collins J, Korona B, Ghalei H, Karbstein K
PLoS Biol
. 2019 Dec;
17(12):e3000329.
PMID: 31834877
Premature release of nascent ribosomes into the translating pool must be prevented because these do not support viability and may be prone to mistakes. Here, we show that the kinase...