Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Tracey D. Myers"'
Autor:
Tracey D. Myers, Yizhi Li, Stefanie Taiclet, Paulina Cabada-Aguirre, Emily Kuti, Kaitlin McClure, Christopher Blanchard, Marta Wolosowicz, Gregg E. Homanics, Adam C. Straub, Stephen D. Meriney, Michael J. Palladino
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract Triosephosphate isomerase deficiency (TPI Df) is a rare multisystem disorder with severe neuromuscular symptoms which arises exclusively from mutations within the TPI1 gene. Studies of TPI Df have been limited due to the absence of mammalian
Externí odkaz:
https://doaj.org/article/cadf9011a35d4760a00e26990a31124a
Autor:
Tracey D. Myers, Michael J. Palladino
Publikováno v:
Molecular Medicine, Vol 29, Iss 1, Pp 1-6 (2023)
Abstract Triosephosphate isomerase (TPI) is best known as a glycolytic enzyme that interconverts the 3-carbon sugars dihydroxyacetone phosphate (DHAP) and glyceraldehyde-3-phosphate (G3P). TPI is an essential enzyme that is required for the catabolis
Externí odkaz:
https://doaj.org/article/502a1e099bdd4a54994f58c3bbedb07f
Autor:
Andrew P. VanDemark, Stacy L. Hrizo, Samantha L. Eicher, Jules Kowalski, Tracey D. Myers, Megan R. Pfeifer, Kacie N. Riley, Dwight D. Koeberl, Michael J. Palladino
Publikováno v:
Disease Models & Mechanisms, Vol 15, Iss 5 (2022)
Triosephosphate isomerase (TPI) deficiency (TPI Df) is an untreatable glycolytic enzymopathy that results in hemolytic anemia, progressive muscular impairment and irreversible brain damage. Although there is a ‘common’ mutation (TPIE105D), other
Externí odkaz:
https://doaj.org/article/6e587810fc2644ddac6db38219dae764
Publikováno v:
Current Research in Neurobiology, Vol 3, Iss , Pp 100062- (2022)
Triosephosphate isomerase deficiency (TPI Df) is a rare, aggressive genetic disease that typically affects young children and currently has no established treatment. TPI Df is characterized by hemolytic anemia, progressive neuromuscular degeneration,
Externí odkaz:
https://doaj.org/article/79c5ac5e12ca420ca08778d42c2affb9
Autor:
Stacy L. Hrizo, Samantha L. Eicher, Tracey D. Myers, Ian McGrath, Andrew P.K. Wodrich, Hemanth Venkatesh, Daniel Manjooran, Sabrina Swoger, Kim Gagnon, Matthew Bruskin, Maria V. Lebedev, Sherry Zheng, Ana Vitantonio, Sungyoun Kim, Zachary J. Lamb, Andreas Vogt, Maura R.Z. Ruzhnikov, Michael J. Palladino
Publikováno v:
Neurobiology of Disease, Vol 152, Iss , Pp 105299- (2021)
Triosephosphate isomerase (TPI) deficiency (Df) is a rare recessive metabolic disorder that manifests as hemolytic anemia, locomotor impairment, and progressive neurodegeneration. Research suggests that TPI Df mutations, including the “common” TP
Externí odkaz:
https://doaj.org/article/40387faf9837432e845ed51feb7d8d99
Autor:
Michael J. Palladino, Stacy L. Hrizo, Tracey D. Myers, E. Michael Meyer, Samantha L. Eicher, Laura L. Vollmer, Andreas Vogt
Publikováno v:
SLAS Discov
Triose phosphate isomerase deficiency (TPI Df) is an untreatable, childhood-onset glycolytic enzymopathy. Patients typically present with frequent infections, anemia, and muscle weakness that quickly progresses with severe neuromusclar dysfunction re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a78b9d7cf55833eb02dbe04ac409cf5b
https://doi.org/10.1177/24725552211018198
https://doi.org/10.1177/24725552211018198
Autor:
Tracey D. Myers, Hemanth Venkatesh, Andrew P.K. Wodrich, Sherry Zheng, Michael J. Palladino, Ana Vitantonio, Sungyoun Kim, Daniel T. Manjooran, Samantha L. Eicher, Kim Gagnon, Ian McGrath, Maria V. Lebedev, Maura R.Z. Ruzhnikov, Zachary J. Lamb, Sabrina Swoger, Stacy L. Hrizo, Matthew Bruskin, Andreas Vogt
Publikováno v:
Neurobiology of disease
Neurobiology of Disease, Vol 152, Iss, Pp 105299-(2021)
Neurobiology of Disease, Vol 152, Iss, Pp 105299-(2021)
Triosephosphate isomerase (TPI) deficiency (Df) is a rare recessive metabolic disorder that manifests as hemolytic anemia, locomotor impairment, and progressive neurodegeneration. Research suggests that TPI Df mutations, including the “common” TP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b00eb62d992842d29282402417175bd
http://europepmc.org/articles/PMC7993632
http://europepmc.org/articles/PMC7993632