Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kelsey Manko"'
Autor:
Emily J Bartley, Meryl J Alappattu, Kelsey Manko, Hannah Lewis, Terrie Vasilopoulos, Georgine Lamvu
Publikováno v:
Women's Health, Vol 20 (2024)
Background: Evidence of overlap between endometriosis and chronic pain conditions is emerging; however, little is known about how the pain experience differs based on the presence or absence of endometriosis. Objectives: In a sample of women reportin
Externí odkaz:
https://doaj.org/article/a5fd996909a84a8590ec77c0346a072d
Autor:
Dorianmarie Vargas-Franco, Peter B. Kang, Chengcheng Li, Madhurima Saha, Rachel Davis, Kelsey Manko, Christina A. Pacak, Isabelle Draper
Publikováno v:
FEBS Open Bio
The exact disease mechanism of MEGF10 deficiency, which causes a rare inherited myopathy, remains unknown. In mice, Megf10 deficiency is associated with slower proliferation and migration of satellite cells, as well as impaired skeletal muscle regene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad77e76958cf001d561e2fd7faf883d0
https://doi.org/10.1002/2211-5463.13031
https://doi.org/10.1002/2211-5463.13031
Autor:
Christine C. Bruels, Satomi Mitsuhashi, Isabelle Draper, Michael D. Jones, Christina A. Pacak, Hemakumar M. Reddy, Kyung Ah Cho, Kelsey Manko, Madhurima Saha, Peter B. Kang
Publikováno v:
Human molecular genetics. 26(15)
Mutations in MEGF10 cause early onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD), a rare congenital muscle disease, but the pathogenic mechanisms remain largely unknown. We demonstrate that short hairpin RNA (shRNA)-mediated kn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7354bda100505149df645c9fcd11addb
https://pubmed.ncbi.nlm.nih.gov/28498977
https://pubmed.ncbi.nlm.nih.gov/28498977
Autor:
Amy Donate, Peter B. Kang, Skylar A. Rizzo, Fowzan S. Alkuraya, Christina A. Pacak, Katherine E. Santostefano, Kelsey Manko, Nao Terada, Michael S. Jones
Publikováno v:
Molecular Therapy. 24:S144
Cockayne Syndrome (CS) is a rare, autosomal recessive, neurodegenerative disorder characterized by deficiencies which all contribute to an overall phenotype of premature aging. The underlying cause is a defect in genes involving DNA repair mechanisms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d133b98e6365298bbd2702a239845eba
https://doi.org/10.1016/s1525-0016(16)33169-0
https://doi.org/10.1016/s1525-0016(16)33169-0