Ellyn L Peterson
Overview
Explore the profile of Ellyn L Peterson including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
5
Citations
88
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Potter R, Peterson E, Griffin D, Cooper Olson G, Lewis S, Cochran K, et al.
Mol Ther Methods Clin Dev
. 2024 Feb;
32(1):101195.
PMID: 38327805
Patients with pre-existing immunity to adeno-associated virus (AAV) are currently unable to receive systemic gene transfer therapies. In this nonhuman primate study, we investigated the impact of immunosuppression strategies on...
2.
Seo Y, Baine S, Kempton A, Rogers O, Lewis S, Adegboye K, et al.
Mol Ther Methods Clin Dev
. 2023 Feb;
28:284-299.
PMID: 36816759
Limb-girdle muscular dystrophy (LGMD) type 2C/R5 results from mutations in the γ-sarcoglycan () gene and is characterized by muscle weakness and progressive wasting. Loss of functional γ-sarcoglycan protein in the...
3.
Potter R, Griffin D, Heller K, Peterson E, Clark E, Mendell J, et al.
Hum Gene Ther
. 2021 Jan;
32(7-8):375-389.
PMID: 33397205
Duchenne muscular dystrophy (DMD) is a rare, X-linked, fatal, degenerative neuromuscular disease caused by mutations in the gene. More than 2,000 mutations of the gene are responsible for progressive loss...
4.
Griffin D, Pozsgai E, Heller K, Potter R, Peterson E, Rodino-Klapac L
Hum Gene Ther
. 2020 Dec;
32(7-8):390-404.
PMID: 33349138
Limb-girdle muscular dystrophy type 2D/R3 (LGMD2D/R3) is a progressive muscular dystrophy that manifests with muscle weakness, respiratory abnormalities, and in rare cases cardiomyopathy. LGMD2D/R3 is caused by mutations in the...
5.
Potter R, Griffin D, Sondergaard P, Johnson R, Pozsgai E, Heller K, et al.
Hum Gene Ther
. 2017 Jul;
29(7):749-762.
PMID: 28707952
Dysferlinopathies comprise a family of disorders caused by mutations in the dysferlin (DYSF) gene, leading to a progressive dystrophy characterized by chronic muscle fiber loss, fat replacement, and fibrosis. To...