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
Citations
8805
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Recent Articles
21.
Herrador A, Fedeli C, Radulovic E, Campbell K, Moreno H, Gerold G, et al.
mBio
. 2019 Mar;
10(2).
PMID: 30914516
Recognition of functional receptors by viruses is a key determinant for their host range, tissue tropism, and disease potential. The highly pathogenic Lassa virus (LASV) currently represents one of the...
22.
Gonzalez Coraspe J, Weis J, Anderson M, Munchberg U, Lorenz K, Buchkremer S, et al.
Skelet Muscle
. 2018 Aug;
8(1):28.
PMID: 30153853
Background: Caveolin-3 (CAV3) is a muscle-specific protein localized to the sarcolemma. It was suggested that CAV3 is involved in the connection between the extracellular matrix (ECM) and the cytoskeleton. Caveolinopathies...
23.
Brun B, Willer T, Darbro B, Gonorazky H, Naumenko S, Dowling J, et al.
Neuromuscul Disord
. 2018 May;
28(7):592-596.
PMID: 29759639
Mutations in POMT2 are most commonly associated with Walker-Warburg syndrome and Muscle-Eye-Brain disease, but can also cause limb girdle muscular dystrophy (LGMD2N). We report a case of LGMD due to...
24.
Clements R, Turk R, Campbell K, Wright K
J Neurosci
. 2017 Aug;
37(35):8559-8574.
PMID: 28760865
Proper neural circuit formation requires the precise regulation of neuronal migration, axon guidance, and dendritic arborization. Mutations affecting the function of the transmembrane glycoprotein dystroglycan cause a form of congenital...
25.
Cox M, Evans J, Davis A, Guo L, Levy J, Starr-Moss A, et al.
Skelet Muscle
. 2017 Jul;
7(1):15.
PMID: 28697784
Background: Limb-girdle muscular dystrophies (LGMDs) are a heterogeneous group of inherited autosomal myopathies that preferentially affect voluntary muscles of the shoulders and hips. LGMD has been clinically described in several...
26.
Zhu Q, Venzke D, Walimbe A, Anderson M, Fu Q, Kinch L, et al.
Elife
. 2016 Nov;
5.
PMID: 27879205
The 'pseudokinase' SgK196 is a protein O-mannose kinase (POMK) that catalyzes an essential phosphorylation step during biosynthesis of the laminin-binding glycan on α-dystroglycan. However, the catalytic mechanism underlying this activity...
27.
Jerber J, Zaki M, Al-Aama J, Rosti R, Ben-Omran T, Dikoglu E, et al.
Am J Hum Genet
. 2016 Nov;
99(5):1181-1189.
PMID: 27773428
Cobblestone lissencephaly (COB) is a severe brain malformation in which overmigration of neurons and glial cells into the arachnoid space results in the formation of cortical dysplasia. COB occurs in...
28.
Fruh S, Romanos J, Panzanelli P, Burgisser D, Tyagarajan S, Campbell K, et al.
J Neurosci
. 2016 Oct;
36(40):10296-10313.
PMID: 27707967
Significance Statement: Dystroglycan, an extracellular and transmembrane protein of the dystrophin-glycoprotein complex, is at the center of molecular studies of muscular dystrophies. Although its synaptic distribution in cortical brain regions...
29.
Rader E, Turk R, Willer T, Beltran D, Inamori K, Peterson T, et al.
Proc Natl Acad Sci U S A
. 2016 Sep;
113(39):10992-7.
PMID: 27625424
Dystroglycan (DG) is a highly expressed extracellular matrix receptor that is linked to the cytoskeleton in skeletal muscle. DG is critical for the function of skeletal muscle, and muscle with...
30.
Briggs D, Yoshida-Moriguchi T, Zheng T, Venzke D, Anderson M, Strazzulli A, et al.
Nat Chem Biol
. 2016 Aug;
12(10):810-4.
PMID: 27526028
Dystroglycan is a highly glycosylated extracellular matrix receptor with essential functions in skeletal muscle and the nervous system. Reduced matrix binding by α-dystroglycan (α-DG) due to perturbed glycosylation is a...