Daniel E Michele
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Explore the profile of Daniel E Michele including associated specialties, affiliations and a list of published articles.
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55
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2402
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Recent Articles
11.
Garbincius J, Merz L, Cuttitta A, Bayne K, Schrade S, Armstead E, et al.
Am J Physiol Heart Circ Physiol
. 2020 Aug;
319(3):H582-H603.
PMID: 32762558
Duchenne muscular dystrophy (DMD) is an X-linked disease caused by null mutations in dystrophin and characterized by muscle degeneration. Cardiomyopathy is common and often prevalent at similar frequency in female...
12.
Evers S, Kim K, Bozadjieva N, Lewis A, Farris D, Sorensen M, et al.
Mol Metab
. 2020 Feb;
32:148-159.
PMID: 32029224
Objective: Post-bariatric surgery hypoglycemia (PBH) is defined as the presence of neuroglycopenic symptoms accompanied by postprandial hypoglycemia in bariatric surgery patients. Recent clinical studies using continuous glucose monitoring (CGM) technology...
13.
Schwartz A, Converso-Baran K, Michele D, Shah Y
J Biol Chem
. 2019 Aug;
294(41):14991-15002.
PMID: 31416832
Iron is a micronutrient fundamental for life. Iron homeostasis in mammals requires sustained postnatal intestinal iron absorption that maintains intracellular iron concentrations for central and systemic metabolism as well as...
14.
Eisen B, Ben Jehuda R, Cuttitta A, Mekies L, Shemer Y, Baskin P, et al.
J Cell Mol Med
. 2019 Jan;
23(3):2125-2135.
PMID: 30618214
Duchenne muscular dystrophy (DMD) is an X-linked progressive muscle degenerative disease, caused by mutations in the dystrophin gene and resulting in death because of respiratory or cardiac failure. To investigate...
15.
Buras E, Converso-Baran K, Davis C, Akama T, Hikage F, Michele D, et al.
Diabetes
. 2018 Oct;
68(1):45-56.
PMID: 30361289
Respiratory dysfunction is a common complication of obesity, conferring cardiovascular morbidity and increased mortality and often necessitating mechanical ventilatory support. While impaired lung expansion in the setting of increased adipose...
16.
Eisen B, Ben Jehuda R, Cuttitta A, Mekies L, Reiter I, Ramchandren S, et al.
Stem Cell Res
. 2018 Apr;
29:111-114.
PMID: 29653394
Duchenne muscular dystrophy (DMD) is an X-linked progressive muscle degenerative disease caused by mutations in the dystrophin gene. We generated induced pluripotent stem cells (iPSCs) from a 13-year-old male patient...
17.
Sahinoz M, Khairi S, Cuttitta A, Brady G, Rupani A, Meral R, et al.
Clin Diabetes Endocrinol
. 2018 Apr;
4:6.
PMID: 29610677
Background: Juvenile dermatomyositis (JDM) is an auto-immune muscle disease which presents with skin manifestations and muscle weakness. At least 10% of the patients with JDM present with acquired lipodystrophy. Laminopathies...
18.
Campbell M, Witcher M, Gopal A, Michele D
Am J Physiol Heart Circ Physiol
. 2016 Mar;
310(9):H1140-50.
PMID: 26968544
Delta-sarcoglycan is a component of the sarcoglycan subcomplex within the dystrophin-glycoprotein complex located at the plasma membrane of muscle cells. While recessive mutations in δ-sarcoglycan cause limb girdle muscular dystrophy...
19.
Kim E, Galchev V, Kim J, Misek S, Stevenson T, Campbell M, et al.
Proteomics Clin Appl
. 2016 Jan;
10(5):585-96.
PMID: 26756417
Purpose: A goal of this study was to identify and investigate previously unrecognized components of the remodeling process in the progression to heart failure by comparing protein expression in ischemic...
20.
Garbincius J, Michele D
Proc Natl Acad Sci U S A
. 2015 Oct;
112(44):13663-8.
PMID: 26483453
Patients deficient in dystrophin, a protein that links the cytoskeleton to the extracellular matrix via the dystrophin-glycoprotein complex (DGC), exhibit muscular dystrophy, cardiomyopathy, and impaired muscle nitric oxide (NO) production....