Kevin P. Campbell, Ph.D, University of Rochester 1976
Affiliations: | Physiology & Biophysics and Neurology | University of Iowa, Iowa City, IA |
Area:
Ion channels, muscle pathologyWebsite:
http://www.physiology.uiowa.edu/campbell/Google:
"Kevin Campbell"Bio:
https://campbell.lab.uiowa.edu/
https://digital.library.unt.edu/ark:/67531/metadc1204525/
Mean distance: 18.18 (cluster 46) | S | N | B | C | P |
Cross-listing: Chemistry Tree
Parents
Sign in to add mentor| Adil E. Shamoo | grad student | 1978 | Rochester (Physiology Academic Tree) | |
| (Biochemical and morphological characterization of light and heavy sarcoplasmic reticulum vesicles.) | ||||
| David H. MacLennan | post-doc | University of Toronto | ||
Children
Sign in to add trainee| Daniel E. Michele | grad student | University of Iowa (Cell & Gene Therapy Tree) | |
| Leland E. Lim | grad student | 2000 | University of Iowa |
| Jyothi Arikkath | grad student | 2003 | University of Iowa |
| Dimple Bansal | grad student | 2003 | University of Iowa |
| Jakob S. Satz | grad student | 2007 | University of Iowa |
| Rachelle H. Crosbie | post-doc | University of Iowa | |
| Michel DeWaard | post-doc | University of Iowa | |
| Renzhi Han | post-doc | University of Iowa | |
| John Lueck | post-doc | University of Iowa | |
| James M. Ervasti | post-doc | 1989-1992 | University of Iowa |
BETA: Related publications
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Publications
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| Shelton GD, Minor KM, Guo LT, et al. (2021) Muscular dystrophy-dystroglycanopathy in a family of Labrador retrievers with a LARGE1 mutation. Neuromuscular Disorders : Nmd |
| Bez Batti Angulski A, Bauer J, Cohen H, et al. (2020) Investigations of an inducible intact dystrophin gene excision system in cardiac and skeletal muscle in vivo. Scientific Reports. 10: 10967 |
| Beltrán D, Anderson ME, Bharathy N, et al. (2019) Exogenous expression of the glycosyltransferase LARGE1 restores α-dystroglycan matriglycan and laminin binding in rhabdomyosarcoma. Skeletal Muscle. 9: 11 |
| González Coraspe JA, Weis J, Anderson ME, et al. (2018) Biochemical and pathological changes result from mutated Caveolin-3 in muscle. Skeletal Muscle. 8: 28 |
| Brun BN, Willer T, Darbro BW, et al. (2018) Uniparental disomy unveils a novel recessive mutation in POMT2. Neuromuscular Disorders : Nmd |
| Clements R, Turk R, Campbell KP, et al. (2017) Dystroglycan Maintains Inner Limiting Membrane Integrity to Coordinate Retinal Development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Cox ML, Evans JM, Davis AG, et al. (2017) Exome sequencing reveals independent SGCD deletions causing limb girdle muscular dystrophy in Boston terriers. Skeletal Muscle. 7: 15 |
| Jerber J, Zaki MS, Al-Aama JY, et al. (2016) Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly. American Journal of Human Genetics |
| Früh S, Romanos J, Panzanelli P, et al. (2016) Neuronal Dystroglycan Is Necessary for Formation and Maintenance of Functional CCK-Positive Basket Cell Terminals on Pyramidal Cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 10296-10313 |
| Rader EP, Turk R, Willer T, et al. (2016) Role of dystroglycan in limiting contraction-induced injury to the sarcomeric cytoskeleton of mature skeletal muscle. Proceedings of the National Academy of Sciences of the United States of America |