Katherine G English
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Explore the profile of Katherine G English including associated specialties, affiliations and a list of published articles.
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6
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26
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Recent Articles
1.
Huang L, Simonian R, Lopez M, Karuppasamy M, Sanders V, English K, et al.
EMBO Mol Med
. 2025 Feb;
PMID: 39994482
X-linked myopathy with excessive autophagy (XMEA), a rare childhood-onset autophagic vacuolar myopathy caused by mutations in VMA21, is characterized by proximal muscle weakness and progressive vacuolation. VMA21 encodes a protein...
2.
Karuppasamy M, English K, Conner J, Rorrer S, Lopez M, Crossman D, et al.
bioRxiv
. 2025 Feb;
PMID: 39975305
Duchenne muscular dystrophy (DMD) patients suffer from skeletal and cardiopulmonary weakness, and interestingly up to one third are diagnosed on the autism spectrum. Dystrophin is an essential protein for regulating...
3.
Karuppasamy M, English K, Henry C, Manzini M, Parant J, Wright M, et al.
Dis Model Mech
. 2024 Jan;
17(1).
PMID: 38235578
Skeletal muscular diseases predominantly affect skeletal and cardiac muscle, resulting in muscle weakness, impaired respiratory function and decreased lifespan. These harmful outcomes lead to poor health-related quality of life and...
4.
Samani A, Karuppasamy M, English K, Siler C, Wang Y, Widrick J, et al.
FASEB J
. 2023 Sep;
37(10):e23198.
PMID: 37742307
DOCK (dedicator of cytokinesis) is an 11-member family of typical guanine nucleotide exchange factors (GEFs) expressed in the brain, spinal cord, and skeletal muscle. Several DOCK proteins have been implicated...
5.
Samani A, Karuppasamy M, English K, Siler C, Wang Y, Widrick J, et al.
bioRxiv
. 2023 Mar;
PMID: 36865261
DOCK (dedicator of cytokinesis) is an 11-member family of typical guanine nucleotide exchange factors (GEFs) expressed in the brain, spinal cord, and skeletal muscle. Several DOCK proteins have been implicated...
6.
English K, Reid A, Samani A, Coulis G, Villalta S, Walker C, et al.
Biomedicines
. 2022 Oct;
10(10).
PMID: 36289662
Duchenne muscular dystrophy (DMD) is a progressive, X-linked childhood neuromuscular disorder that results from loss-of-function mutations in the DYSTROPHIN gene. DMD patients exhibit muscle necrosis, cardiomyopathy, respiratory failure, and loss...
7.
Samani A, English K, Lopez M, Birch C, Brown D, Kaur G, et al.
Hum Mutat
. 2022 May;
43(9):1149-1161.
PMID: 35544951
The Dedicator of Cytokinesis (DOCK) family (DOCK1-11) of genes are essential mediators of cellular migration, growth, and fusion in a variety of cell types and tissues. Recent advances in whole-genome...
8.
Samani A, Hightower R, Reid A, English K, Lopez M, Doyle J, et al.
Life Sci Alliance
. 2022 May;
5(9).
PMID: 35512829
miR-486 is a muscle-enriched microRNA, or "myomiR," that has reduced expression correlated with Duchenne muscular dystrophy (DMD). To determine the function of miR-486 in normal and dystrophin-deficient muscles and elucidate...