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of 6
pro vyhledávání: '"Kristen E. Bergquist"'
Autor:
Emily N. Cronin-Furman, Jennifer Barber-Singh, Kristen E. Bergquist, Takao Yagi, Patricia A. Trimmer
Publikováno v:
Biomolecules, Vol 9, Iss 4, p 119 (2019)
Parkinson’s disease (PD) is a neurodegenerative disorder that exhibits aberrant protein aggregation and mitochondrial dysfunction. Ndi1, the yeast mitochondrial NADH dehydrogenase (complex I) enzyme, is a single subunit, internal matrix-facing prot
Externí odkaz:
https://doaj.org/article/dff8c86f4e774f288a4c74261319d47a
Autor:
Kristen E. Bergquist, Kathleen M. Schwarz, Patricia A. Trimmer, Shilpa Iyer, Ravindar R. Thomas, Christina M. Papageorge, James P. Bennett, Shaharyar M. Khan, Lisa D. Dunham, Caitlin K. Quigley, Paula M. Keeney, Francisco R. Portell
Publikováno v:
Human Gene Therapy. 20:897-907
Neurodegeneration in Parkinson's disease (PD) affects mainly dopaminergic neurons in the substantia nigra, where age-related, increasing percentages of cells lose detectable respiratory activity associated with depletion of intact mitochondrial DNA (
Autor:
Emily N. Cronin-Furman, Kristen E. Bergquist, Patricia A. Trimmer, M. Kathleen Borland, James P. Bennett
Publikováno v:
Molecular Neurodegeneration, Vol 8, Iss 1, p 6 (2013)
Molecular Neurodegeneration
Molecular Neurodegeneration
Background Lewy bodies (LB) are a neuropathological hallmark of Parkinson’s disease (PD) and other synucleinopathies. The role their formation plays in disease pathogenesis is not well understood, in part because studies of LB have been limited to
Autor:
Shilpa Iyer, Raj R. Rao, James P. Bennett, Erich Gnaiger, Kisha J. Young, Kristen E. Bergquist
Publikováno v:
Human gene therapy. 23(6)
Many incurable mitochondrial disorders result from mutant mitochondrial DNA (mtDNA) and impaired respiration. Leigh's syndrome (LS) is a fatal neurodegenerative disorder of infants, and Leber's hereditary optic neuropathy (LHON) causes blindness in y
Autor:
Caitlin K. Quigley, Kristen E. Bergquist, Stephanie L. Morton, Paula M. Keeney, James P. Bennett, Lisa D. Dunham
Sporadic Parkinson's disease (sPD) is a nervous system-wide disease that presents with a bradykinetic movement disorder and frequently progresses to include depression and cognitive impairment. Cybrid models of sPD are based on expression of sPD plat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc24c93aa89f601a455181b6773de53e
https://europepmc.org/articles/PMC2783275/
https://europepmc.org/articles/PMC2783275/
Autor:
Paula M. Keeney, Caitlin K. Quigley, Lisa D. Dunham, Christina M. Papageorge, Shilpa Iyer, Ravindar R. Thomas, Kathleen M. Schwarz, Patricia A. Trimmer, Shaharyar M. Khan, Francisco R. Portell, Kristen E. Bergquist, James P. Bennett
Publikováno v:
Human Gene Therapy; Aug2009, Vol. 20 Issue 8, p897-907, 11p