Kevin P Campbell
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Explore the profile of Kevin P Campbell including associated specialties, affiliations and a list of published articles.
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172
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8805
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Recent Articles
11.
Shelton G, Minor K, Guo L, Friedenberg S, Cullen J, Hord J, et al.
Neuromuscul Disord
. 2021 Oct;
31(11):1169-1178.
PMID: 34654610
Alpha-dystroglycan (αDG) is a highly glycosylated cell surface protein with a significant role in cell-to-extracellular matrix interactions in muscle. αDG interaction with extracellular ligands relies on the activity of the...
12.
Joseph S, Campbell K
Viruses
. 2021 Sep;
13(9).
PMID: 34578260
Lassa fever virus (LASV) can cause life-threatening hemorrhagic fevers for which there are currently no vaccines or targeted treatments. The late Prof. Stefan Kunz, along with others, showed that the...
13.
Walimbe A, Okuma H, Joseph S, Yang T, Yonekawa T, Hord J, et al.
Elife
. 2020 Sep;
9.
PMID: 32975514
Matriglycan [-GlcA-β1,3-Xyl-α1,3-] serves as a scaffold in many tissues for extracellular matrix proteins containing laminin-G domains including laminin, agrin, and perlecan. Like-acetyl-glucosaminyltransferase 1 (LARGE1) synthesizes and extends matriglycan on α-dystroglycan...
14.
Bez Batti Angulski A, Bauer J, Cohen H, Kobuke K, Campbell K, Metzger J
Sci Rep
. 2020 Jul;
10(1):10967.
PMID: 32620803
We sought here to induce the excision of a large intragenic segment within the intact dystrophin gene locus, with the ultimate goal to elucidate dystrophin protein function and stability in...
15.
Sheikh M, Venzke D, Anderson M, Yoshida-Moriguchi T, Glushka J, Nairn A, et al.
Glycobiology
. 2020 Mar;
30(10):817-829.
PMID: 32149355
Mutations in multiple genes required for proper O-mannosylation of α-dystroglycan are causal for congenital/limb-girdle muscular dystrophies and abnormal brain development in mammals. Previously, we and others further elucidated the functional...
16.
Day B, Lathia J, Bruce Z, DSouza R, Baumgartner U, Ensbey K, et al.
Acta Neuropathol
. 2019 Aug;
138(6):1033-1052.
PMID: 31463571
Glioblastomas (GBMs) are malignant central nervous system (CNS) neoplasms with a very poor prognosis. They display cellular hierarchies containing self-renewing tumourigenic glioma stem cells (GSCs) in a complex heterogeneous microenvironment....
17.
Ware B, Sullivan B, LaVergne S, Marro B, Egashira T, Campbell K, et al.
Proc Natl Acad Sci U S A
. 2019 Aug;
116(36):18001-18008.
PMID: 31427525
Lymphocytic choriomeningitis virus (LCMV) WE variant 2.2 (v2.2) generated a high level of the major mouse urinary protein: MUP. Mice infected with LCMV WE v54, which differed from v2.2 by...
18.
de Greef J, Slutter B, Anderson M, Hamlyn R, OCampo Landa R, McNutt E, et al.
Proc Natl Acad Sci U S A
. 2019 May;
116(23):11396-11401.
PMID: 31097590
α-Dystroglycan (α-DG) is a highly glycosylated basement membrane receptor that is cleaved by the proprotein convertase furin, which releases its N-terminal domain (α-DGN). Before cleavage, α-DGN interacts with the glycosyltransferase...
19.
Beltran D, Anderson M, Bharathy N, Settelmeyer T, Svalina M, Bajwa Z, et al.
Skelet Muscle
. 2019 May;
9(1):11.
PMID: 31054580
Background: α-Dystroglycan is the highly glycosylated component of the dystrophin-glycoprotein complex (DGC) that binds with high-affinity to extracellular matrix (ECM) proteins containing laminin-G-like (LG) domains via a unique heteropolysaccharide [-GlcA-beta1,3-Xyl-alpha1,3-]...
20.
Chakravorty S, Berger K, Arafat D, Nallamilli B, Subramanian H, Joseph S, et al.
Muscle Nerve
. 2019 Apr;
60(1):98-103.
PMID: 30990900
Introduction: UDP N-acetylglucosamine2-epimerase/N-acetylmannosamine-kinase (GNE) gene mutations can cause mostly autosomal-recessive myopathy with juvenile-onset known as hereditary inclusion-body myopathy (HIBM). Methods: We describe a family of a patient showing an unusual...