Katherine S Fallon
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Explore the profile of Katherine S Fallon including associated specialties, affiliations and a list of published articles.
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7
Citations
143
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Recent Articles
1.
Southern W, Johnson E, Fasbender E, Fallon K, Cavazos C, Lowe D, et al.
J Clin Invest
. 2025 Jan;
135(5).
PMID: 39808494
Eccentric contraction-induced (ECC-induced) force loss is a hallmark of murine dystrophin-deficient (mdx) skeletal muscle that is used to assess efficacy of potential therapies for Duchenne muscular dystrophy. While virtually all...
2.
Demonbreun A, Bogdanovic E, Vaught L, Reiser N, Fallon K, Long A, et al.
JCI Insight
. 2022 Jul;
7(14).
PMID: 35866481
Membrane instability and disruption underlie myriad acute and chronic disorders. Anxa6 encodes the membrane-associated protein annexin A6 and was identified as a genetic modifier of muscle repair and muscular dystrophy....
3.
Demonbreun A, Fallon K, Oosterbaan C, Vaught L, Reiser N, Bogdanovic E, et al.
Sci Transl Med
. 2021 Sep;
13(610):eabf0376.
PMID: 34516828
Duchenne muscular dystrophy, like other muscular dystrophies, is a progressive disorder hallmarked by muscle degeneration, inflammation, and fibrosis. Latent transforming growth factor β (TGFβ) binding protein 4 (LTBP4) is an...
4.
McDade T, McNally E, Zelikovich A, DAquila R, Mustanski B, Miller A, et al.
PLoS One
. 2020 Aug;
15(8):e0237833.
PMID: 32797108
Objective: Serological testing is needed to investigate the extent of transmission of SARS-CoV-2 from front-line essential workers to their household members. However, the requirement for serum/plasma limits serological testing to...
5.
Demonbreun A, Wyatt E, Fallon K, Oosterbaan C, Page P, Hadhazy M, et al.
Dis Model Mech
. 2019 Oct;
13(2).
PMID: 31582396
Limb-girdle muscular dystrophy type 2C is caused by autosomal recessive mutations in the γ-sarcoglycan () gene. The most common mutation is a single nucleotide deletion from a stretch of five...
6.
Demonbreun A, Fallon K, Oosterbaan C, Bogdanovic E, Warner J, Sell J, et al.
J Clin Invest
. 2019 Sep;
129(11):4657-4670.
PMID: 31545299
Membrane repair is essential to cell survival. In skeletal muscle, injury often associates with plasma membrane disruption. Additionally, muscular dystrophy is linked to mutations in genes that produce fragile membranes...
7.
Aubert G, Barefield D, Demonbreun A, Ramratnam M, Fallon K, Warner J, et al.
JACC Basic Transl Sci
. 2019 May;
4(2):251-268.
PMID: 31061927
The adult myocardium relies on oxidative metabolism. In ischemic myocardium, such as the embryonic heart, glycolysis contributes more prominently as a fuel source. The sulfonylurea receptor 2 (SUR2) was previously...
8.
Vo A, Swaggart K, Woo A, Gao Q, Demonbreun A, Fallon K, et al.
Hum Mol Genet
. 2018 Oct;
28(2):279-289.
PMID: 30289454
Like other single-gene disorders, muscular dystrophy displays a range of phenotypic heterogeneity even with the same primary mutation. Identifying genetic modifiers capable of altering the course of muscular dystrophy is...